Genetic counseling (English Wikipedia)

Australasian Association of Genetic Counsellors. "HGSA Certification for Genetic Counsellors". Human Genetics Society of Australasia.
"Home". www.asgc.org.au. Archived from the original on 2024-07-21. Retrieved 2025-01-13.

asu.edu

embryo.asu.edu

"Sheldon Clark Reed (1910–2003)". The Embryo Project Encyclopedia.
"The Embryo Project Encyclopedia". The National Society of Genetic Counselors (NSGC). Retrieved 2018-09-12.

bls.gov

Bureau of Labor Statistics. "Genetic Counselors: Occupational Outlook Handbook". bls.gov. U.S. Department of Labor. Retrieved 2020-09-27.

cancer.gov

"Genetic Testing for Hereditary Cancer Syndromes". National Cancer Institute. 2013-04-22. Retrieved 2016-03-25.

cancer.org

The American Cancer Society medical and editorial content team. "Family Cancer Syndromes". American Cancer Society. Archived from the original on 2013-08-02. Retrieved 2016-03-25.

cbgc.org.cn

"中国遗传学会遗传咨询分会". cbgc.org.cn. Retrieved 23 March 2018.

cf.ac.uk

orca.cf.ac.uk

Giegling I, Hosak L, Mössner R, Serretti A, Bellivier F, Claes S, et al. (October 2017). "Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics" (PDF). The World Journal of Biological Psychiatry. 18 (7): 492–505. doi:10.1080/15622975.2016.1268715. PMID 28112043. S2CID 4662474.

doi.org

Patch C, Middleton A (June 2018). "Genetic counselling in the era of genomic medicine". British Medical Bulletin. 126 (1): 27–36. doi:10.1093/bmb/ldy008. PMC 5998955. PMID 29617718.
Resta R, Biesecker BB, Bennett RL, Blum S, Hahn SE, Strecker MN, Williams JL (April 2006). "A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report". Journal of Genetic Counseling. 15 (2): 77–83. doi:10.1007/s10897-005-9014-3. PMID 16761103. S2CID 25809385.
Veach PM, LeRoy BS, Bartels DM (2003). Facilitating the Genetic Counselling Process. Springer. doi:10.1007/978-3-319-74799-6. ISBN 978-3-319-74798-9. S2CID 13808432.
Reed SC (December 1974). "A short history of genetic counseling". Social Biology. 21 (4): 332–9. doi:10.1080/19485565.1974.9988131. PMID 4619717.
Kessler S (May 1984). "Book Review: A Genetic Counseling CasebookA Genetic Counseling Casebook. Edited by Gordon ApplebaumEleanor and FiresteinStephen K.New York: Free Press, 1983. 291 pp.$19.95". Social Casework. 65 (5): 314–316. doi:10.1177/104438948406500509. S2CID 80622038.
Veach PM, Bartels DM, Leroy BS (December 2007). "Coming full circle: a reciprocal-engagement model of genetic counseling practice". Journal of Genetic Counseling. 16 (6): 713–28. doi:10.1007/s10897-007-9113-4. PMID 17934802.
Biesecker BB (2016-08-16). "Genetic Counselling: Psychological Issues". ELS. John Wiley & Sons, Ltd. pp. 1–5. doi:10.1002/9780470015902.a0005616.pub3. ISBN 978-0-470-01590-2.
Biesecker B, Austin J, Caleshu C (April 2017). "Response to A Different Vantage Point Commentary: Psychotherapeutic Genetic Counseling, Is it?". Journal of Genetic Counseling. 26 (2): 334–336. doi:10.1007/s10897-016-0025-z. PMC 5383505. PMID 27804046.
Austin J, Semaka A, Hadjipavlou G (December 2014). "Conceptualizing genetic counseling as psychotherapy in the era of genomic medicine". Journal of Genetic Counseling. 23 (6): 903–9. doi:10.1007/s10897-014-9728-1. PMC 4318692. PMID 24841456.
Hodgson JM, Gillam LH, Sahhar MA, Metcalfe SA (February 2010). ""Testing times, challenging choices": an Australian study of prenatal genetic counseling". Journal of Genetic Counseling. 19 (1): 22–37. doi:10.1007/s10897-009-9248-6. PMID 19798554. S2CID 10085887.
Dolan SM (August 2009). "Prenatal genetic testing". Pediatric Annals. 38 (8): 426–30. doi:10.3928/00904481-20090723-05. PMID 19711880.
Madlensky L, Trepanier AM, Cragun D, Lerner B, Shannon KM, Zierhut H (June 2017). "A Rapid Systematic Review of Outcomes Studies in Genetic Counseling". Journal of Genetic Counseling. 26 (3): 361–378. doi:10.1007/s10897-017-0067-x. PMID 28168332.
Corpas M (June 2012). "A family experience of personal genomics". Journal of Genetic Counseling. 21 (3): 386–91. doi:10.1007/s10897-011-9473-7. PMID 22223063. S2CID 10845045.
Gilchrist DM (October 2002). "Medical genetics: 3. An approach to the adult with a genetic disorder". CMAJ. 167 (9): 1021–9. doi:10.1007/s10897-011-9473-7. PMC 134180. PMID 12403743.
Goldberg-Strassler D, Cabey R, Armenti EM, Jordan A (September 2016). "Preimplantation genetic diagnosis (PGD) genetic counseling; but why? The patient experience". Fertility and Sterility. 106 (3 Supplement): e370. doi:10.1016/j.fertnstert.2016.07.1053. ISSN 0015-0282.
Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C, et al. (December 2013). "HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013". Heart Rhythm. 10 (12): 1932–63. doi:10.1016/j.hrthm.2013.05.014. PMID 24011539.
Hershberger RE, Givertz MM, Ho CY, Judge DP, Kantor PF, McBride KL, et al. (May 2018). "Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline". Journal of Cardiac Failure. 24 (5): 281–302. doi:10.1016/j.cardfail.2018.03.004. hdl:1805/15853. PMC 9903357. PMID 29567486.
Gersh BJ, Maron BJ, Bonow RO, Dearani JA, Fifer MA, Link MS, et al. (December 2011). "2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines". Circulation. 124 (24): e783-831. doi:10.1161/CIR.0b013e318223e2bd. PMID 22068434.
Elliott PM, Anastasakis A, Borger MA, Borggrefe M, Cecchi F, Charron P, et al. (October 2014). "2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC)". European Heart Journal. 35 (39): 2733–79. doi:10.1093/eurheartj/ehu284. PMID 25173338.
Goldberg AC, Hopkins PN, Toth PP, Ballantyne CM, Rader DJ, Robinson JG, et al. (June 2011). "Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia". Journal of Clinical Lipidology. 5 (3 Suppl): S1-8. doi:10.1016/j.jacl.2011.04.003. PMID 21600525.
Gidding SS, Champagne MA, de Ferranti SD, Defesche J, Ito MK, Knowles JW, et al. (December 2015). "The Agenda for Familial Hypercholesterolemia: A Scientific Statement From the American Heart Association". Circulation. 132 (22): 2167–92. doi:10.1161/CIR.0000000000000297. PMID 26510694. S2CID 9980924.
Couch FJ, Hart SN, Sharma P, Toland AE, Wang X, Miron P, et al. (February 2015). "Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer". Journal of Clinical Oncology. 33 (4): 304–11. doi:10.1200/jco.2014.57.1414. PMC 4302212. PMID 25452441.
Pritchard CC, Mateo J, Walsh MF, De Sarkar N, Abida W, Beltran H, et al. (August 2016). "Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer". The New England Journal of Medicine. 375 (5): 443–53. doi:10.1056/nejmoa1603144. PMC 4986616. PMID 27433846.
Holter S, Borgida A, Dodd A, Grant R, Semotiuk K, Hedley D, et al. (October 2015). "Germline BRCA Mutations in a Large Clinic-Based Cohort of Patients With Pancreatic Adenocarcinoma". Journal of Clinical Oncology. 33 (28): 3124–9. doi:10.1200/jco.2014.59.7401. PMID 25940717.
Varley JM, McGown G, Thorncroft M, James LA, Margison GP, Forster G, et al. (October 1999). "Are there low-penetrance TP53 Alleles? evidence from childhood adrenocortical tumors". American Journal of Human Genetics. 65 (4): 995–1006. doi:10.1086/302575. PMC 1288270. PMID 10486318.
Lenders JW, Duh QY, Eisenhofer G, Gimenez-Roqueplo AP, Grebe SK, Murad MH, et al. (June 2014). "Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline". The Journal of Clinical Endocrinology and Metabolism. 99 (6): 1915–42. doi:10.1210/jc.2014-1498. PMID 24893135.
Walsh T, Mandell JB, Norquist BM, Casadei S, Gulsuner S, Lee MK, King MC (December 2017). "Genetic Predisposition to Breast Cancer Due to Mutations Other Than BRCA1 and BRCA2 Founder Alleles Among Ashkenazi Jewish Women". JAMA Oncology. 3 (12): 1647–1653. doi:10.1001/jamaoncol.2017.1996. PMC 5824270. PMID 28727877.
Raymond VM, Gray SW, Roychowdhury S, Joffe S, Chinnaiyan AM, Parsons DW, Plon SE (April 2016). "Germline Findings in Tumor-Only Sequencing: Points to Consider for Clinicians and Laboratories". Journal of the National Cancer Institute. 108 (4): djv351. doi:10.1093/jnci/djv351. PMC 4849259. PMID 26590952.
Radtke HB, Sebold CD, Allison C, Haidle JL, Schneider G (August 2007). "Neurofibromatosis type 1 in genetic counseling practice: recommendations of the National Society of Genetic Counselors". Journal of Genetic Counseling. 16 (4): 387–407. doi:10.1007/s10897-007-9101-8. PMC 6338721. PMID 17636453.
Pong AW, Pal DK, Chung WK (May 2011). "Developments in molecular genetic diagnostics: an update for the pediatric epilepsy specialist". Pediatric Neurology. 44 (5): 317–27. doi:10.1016/j.pediatrneurol.2011.01.017. PMID 21481738.
Helbig I, Scheffer IE, Mulley JC, Berkovic SF (March 2008). "Navigating the channels and beyond: unravelling the genetics of the epilepsies". The Lancet. Neurology. 7 (3): 231–45. doi:10.1016/S1474-4422(08)70039-5. PMID 18275925. S2CID 23243066.
Scheffer IE (April 2014). "Epilepsy genetics revolutionizes clinical practice". Neuropediatrics. 45 (2): 70–4. doi:10.1055/s-0034-1371508. PMID 24615646.
Renton AE, Chiò A, Traynor BJ (January 2014). "State of play in amyotrophic lateral sclerosis genetics". Nature Neuroscience. 17 (1): 17–23. doi:10.1038/nn.3584. PMC 4544832. PMID 24369373.
Benatar M, Stanislaw C, Reyes E, Hussain S, Cooley A, Fernandez MC, et al. (June 2016). "Presymptomatic ALS genetic counseling and testing: Experience and recommendations". Neurology. 86 (24): 2295–302. doi:10.1212/WNL.0000000000002773. PMC 4909562. PMID 27194384.
Miles JH (April 2011). "Autism spectrum disorders--a genetics review". Genetics in Medicine. 13 (4): 278–94. doi:10.1097/GIM.0b013e3181ff67ba. PMID 21358411.
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, et al. (May 2010). "Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies". American Journal of Human Genetics. 86 (5): 749–64. doi:10.1016/j.ajhg.2010.04.006. PMC 2869000. PMID 20466091.
Campion D, Dumanchin C, Hannequin D, Dubois B, Belliard S, Puel M, et al. (September 1999). "Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum". American Journal of Human Genetics. 65 (3): 664–70. doi:10.1086/302553. PMC 1377972. PMID 10441572.
Goldman JS, Hahn SE, Catania JW, LaRusse-Eckert S, Butson MB, Rumbaugh M, et al. (June 2011). "Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors". Genetics in Medicine. 13 (6): 597–605. doi:10.1097/GIM.0b013e31821d69b8. PMC 3326653. PMID 21577118.
Crozier S, Robertson N, Dale M (February 2015). "The psychological impact of predictive genetic testing for Huntington's disease: a systematic review of the literature". Journal of Genetic Counseling. 24 (1): 29–39. doi:10.1007/s10897-014-9755-y. PMID 25236481. S2CID 18140209.
Went L (January 1990). "Ethical issues policy statement on Huntington's disease molecular genetics predictive test. International Huntington Association. World Federation of Neurology". Journal of Medical Genetics. 27 (1): 34–8. doi:10.1136/jmg.27.1.34. PMC 1016877. PMID 2137881.
Singleton AB, Farrer MJ, Bonifati V (January 2013). "The genetics of Parkinson's disease: progress and therapeutic implications". Movement Disorders. 28 (1): 14–23. doi:10.1002/mds.25249. PMC 3578399. PMID 23389780.
Trinh J, Farrer M (August 2013). "Advances in the genetics of Parkinson disease". Nature Reviews. Neurology. 9 (8): 445–54. doi:10.1038/nrneurol.2013.132. PMID 23857047. S2CID 31028719.
Pletcher BA, Toriello HV, Noblin SJ, Seaver LH, Driscoll DA, Bennett RL, Gross SJ (June 2007). "Indications for genetic referral: a guide for healthcare providers". Genetics in Medicine. 9 (6): 385–9. doi:10.1097/GIM.0b013e318064e70c. PMC 3110962. PMID 17575505.
Macdonald F (1 November 2008). "Practice of prenatal diagnosis in the UK". Clinical Risk. 14 (6): 218–221. doi:10.1258/cr.2008.080062. S2CID 58245546.
American College of Obstetricians Gynecologists' Committee on Practice Bulletins—Obstetrics; Society for Maternal–Fetal Medicine (May 2016). "Practice Bulletin No. 162: Prenatal Diagnostic Testing for Genetic Disorders". Obstetrics and Gynecology. 127 (5): e108 – e122. doi:10.1097/AOG.0000000000001405. PMID 26938573. S2CID 25791506.
Benn P, Borrell A, Chiu RW, Cuckle H, Dugoff L, Faas B, et al. (August 2015). "Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis". Prenatal Diagnosis. 35 (8): 725–34. doi:10.1002/pd.4608. PMID 25970088. S2CID 23477914.
Gregg AR, Skotko BG, Benkendorf JL, Monaghan KG, Bajaj K, Best RG, et al. (October 2016). "Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics". Genetics in Medicine. 18 (10): 1056–65. doi:10.1038/gim.2016.97. PMID 27467454.
Wilson KL, Czerwinski JL, Hoskovec JM, Noblin SJ, Sullivan CM, Harbison A, et al. (February 2013). "NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy". Journal of Genetic Counseling. 22 (1): 4–15. doi:10.1007/s10897-012-9545-3. PMID 23179172. S2CID 13126623.
Committee On Practice Bulletins—Obstetrics; Committee on Genetics (May 2016). "Practice Bulletin No. 163: Screening for Fetal Aneuploidy". Obstetrics and Gynecology. 127 (5): e123 – e137. doi:10.1097/AOG.0000000000001406. PMID 26938574. S2CID 40095460.
Dugoff L, Norton ME, Kuller JA (October 2016). "The use of chromosomal microarray for prenatal diagnosis". American Journal of Obstetrics and Gynecology. 215 (4): B2-9. doi:10.1016/j.ajog.2016.07.016. PMID 27427470.
International Society for Prenatal Diagnosis; Society for Maternal Fetal Medicine (January 2018). "Joint Position Statement from the International Society for Prenatal Diagnosis (ISPD), the Society for Maternal Fetal Medicine (SMFM), and the Perinatal Quality Foundation (PQF) on the use of genome-wide sequencing for fetal diagnosis". Prenatal Diagnosis. 38 (1): 6–9. doi:10.1002/pd.5195. PMID 29315690.
Grody WW, Thompson BH, Gregg AR, Bean LH, Monaghan KG, Schneider A, Lebo RV (June 2013). "ACMG position statement on prenatal/preconception expanded carrier screening". Genetics in Medicine. 15 (6): 482–3. doi:10.1038/gim.2013.47. PMID 23619275.
"Committee Opinion No. 640: Cell-Free DNA Screening For Fetal Aneuploidy". Obstetrics and Gynecology. 126 (3): e31 – e37. September 2015. doi:10.1097/AOG.0000000000001051. PMID 26287791. S2CID 10876600.
Dondorp W, de Wert G, Bombard Y, Bianchi DW, Bergmann C, Borry P, et al. (April 2015). "Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations". European Journal of Human Genetics. doi:10.1038/ejhg.2015.56. PMID 25828867.
"Committee Opinion No. 690 Summary: Carrier Screening in the Age of Genomic Medicine". Obstetrics and Gynecology. 129 (3): 595–596. March 2017. doi:10.1097/AOG.0000000000001947. PMID 28225420.
Bennett RL, Motulsky AG, Bittles A, Hudgins L, Uhrich S, Doyle DL, et al. (April 2002). "Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic Counselors". Journal of Genetic Counseling. 11 (2): 97–119. doi:10.1023/A:1014593404915. PMID 26141656. S2CID 23922750.
Rothwell E, Johnson E, Mathiesen A, Golden K, Metcalf A, Rose NC, Botkin JR (August 2017). "Experiences among Women with Positive Prenatal Expanded Carrier Screening Results". Journal of Genetic Counseling. 26 (4): 690–696. doi:10.1007/s10897-016-0037-8. PMC 5432405. PMID 27796679.
Stefansdottir V, Skirton H, Jonasson K, Hardardottir H, Jonsson JJ (July 2010). "Effects of knowledge, education, and experience on acceptance of first trimester screening for chromosomal anomalies". Acta Obstetricia et Gynecologica Scandinavica. 89 (7): 931–8. doi:10.3109/00016341003686073. PMID 20235896. S2CID 22380002.
Giegling I, Hosak L, Mössner R, Serretti A, Bellivier F, Claes S, et al. (October 2017). "Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics" (PDF). The World Journal of Biological Psychiatry. 18 (7): 492–505. doi:10.1080/15622975.2016.1268715. PMID 28112043. S2CID 4662474.
Inglis A, Morris E, Austin J (January 2017). "Prenatal genetic counselling for psychiatric disorders". Prenatal Diagnosis. 37 (1): 6–13. doi:10.1002/pd.4878. PMC 5247258. PMID 27466037.
Ryan J, Virani A, Austin JC (June 2015). "Ethical issues associated with genetic counseling in the context of adolescent psychiatry". Applied & Translational Genomics. 5: 23–9. doi:10.1016/j.atg.2015.06.001. PMC 4745399. PMID 26937355.
Demkow U, Wolańczyk T (June 2017). "Genetic tests in major psychiatric disorders-integrating molecular medicine with clinical psychiatry-why is it so difficult?". Translational Psychiatry. 7 (6): e1151. doi:10.1038/tp.2017.106. PMC 5537634. PMID 28608853.
Moldovan R, Pintea S, Austin J (December 2017). "The Efficacy of Genetic Counseling for Psychiatric Disorders: a Meta-Analysis". Journal of Genetic Counseling. 26 (6): 1341–1347. doi:10.1007/s10897-017-0113-8. hdl:2429/68096. PMID 28616830.
Tsuang MT (December 1978). "Genetic counseling for psychiatric patients and their families". The American Journal of Psychiatry. 135 (12): 1465–75. doi:10.1176/ajp.135.12.1465. PMID 717559.
Ormond, Kelly E.; Abad, Peter James; MacLeod, Rhona; Nishigaki, Masakazu; Wessels, Tina-Marié (2024-08-07). "The global status of genetic counselors in 2023: What has changed in the past 5 years?". Genetics in Medicine Open: 101887. doi:10.1016/j.gimo.2024.101887. hdl:20.500.11850/704802. Retrieved 2024-10-11.
Abacan M, Alsubaie L, Barlow-Stewart K, Caanen B, Cordier C, Courtney E, et al. (February 2019). "The Global State of the Genetic Counseling Profession". European Journal of Human Genetics. 27 (2): 183–197. doi:10.1038/s41431-018-0252-x. PMC 6336871. PMID 30291341.
Zhao X, Wang P, Tao X, Zhong N (July 2013). "Genetic services and testing in China". Journal of Community Genetics. 4 (3): 379–90. doi:10.1007/s12687-013-0144-2. PMC 3739851. PMID 23595912.
Li J, Xu T, Yashar BM (September 2015). "Genetics educational needs in China: physicians' experience and knowledge of genetic testing". Genetics in Medicine. 17 (9): 757–60. doi:10.1038/gim.2014.182. PMID 25503494. S2CID 21625217.
Kromberg JG, Wessels TM, Krause A (December 2013). "Roles of genetic counselors in South Africa". Journal of Genetic Counseling. 22 (6): 753–61. doi:10.1007/s10897-013-9606-2. PMID 23723047. S2CID 18335348.
Ormond KE, Laurino MY, Barlow-Stewart K, Wessels TM, Macaulay S, Austin J, Middleton A (March 2018). "Genetic counseling globally: Where are we now?". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 178 (1): 98–107. doi:10.1002/ajmg.c.31607. PMC 5947883. PMID 29575600.
Abacan M, Alsubaie L, Barlow-Stewart K, Caanen B, Cordier C, Courtney E, et al. (February 2019). "The Global State of the Genetic Counseling Profession". European Journal of Human Genetics. 27 (2): 183–197. doi:10.1038/s41431-018-0252-x. PMC 6336871. PMID 30291341.
Isbister, Joanne; Sexton, Adrienne; Forrest, Laura E.; James, Paul; Dowty, James; Taylor, Jessica; Austin, Jehannine; Winship, Ingrid (April 2023). "Psychiatric genetic counseling: A survey of Australian genetic counselors' practice and attitudes". Journal of Genetic Counseling. 32 (2): 495–502. doi:10.1002/jgc4.1659. ISSN 1059-7700. PMID 36480151. S2CID 254478392.
Kanga-Parabia, Anaita; Mitchell, Lucas; Smyth, Renee; Kapoor, Trisha; Duggal, Jaitika; Pearn, Amy; Williams, Rachel; Courtney, Eliza; Edwards, Emma; Bowman, Michelle; Belekar, Mithila; Nisselle, Amy; Pearn, Amy; Kanga-Parabia, Anaita; Lundie, Ben (2024-05-07). "Genetic counseling workforce diversity, inclusion, and capacity in Australia and New Zealand". Genetics in Medicine Open: 101848. doi:10.1016/j.gimo.2024.101848. ISSN 2949-7744. PMC 11658314.
Balobaid A, Qari A, Al-Zaidan H (March 2016). "Genetic counselors' scope of practice and challenges in genetic counseling services in Saudi Arabia". International Journal of Pediatrics & Adolescent Medicine. 3 (1): 1–6. doi:10.1016/j.ijpam.2015.12.002. PMC 6372413. PMID 30805460.
Gallagher TM, Bucciarelli M, Kavalukas SL, Baker MJ, Saunders BD (September 2017). "Attitudes toward genetic counseling and testing in patients with inherited endocrinopathies". Endocrine Practice. 23 (9): 1039–1044. doi:10.4158/EP171875.OR. PMID 28613942.
Haga SB, Barry WT, Mills R, Ginsburg GS, Svetkey L, Sullivan J, Willard HF (April 2013). "Public knowledge of and attitudes toward genetics and genetic testing". Genetic Testing and Molecular Biomarkers. 17 (4): 327–35. doi:10.1089/gtmb.2012.0350. PMC 3609633. PMID 23406207.
Scuffham TM, McInerny-Leo A, Ng SK, Mellick G (April 2014). "Knowledge and attitudes towards genetic testing in those affected with Parkinson's disease". Journal of Community Genetics. 5 (2): 167–77. doi:10.1007/s12687-013-0168-7. PMC 3955457. PMID 24018619.
Singer E, Couper MP, Raghunathan TE, Van Hoewyk J, Antonucci TC (Fall 2008). "Trends in U.S. Attitudes Toward Genetic Testing, 1990-2004". Public Opinion Quarterly. 72 (3): 446–458. doi:10.1093/poq/nfn033. PMC 3045776. PMID 22476359.
Halbert CH, Harrison BW (March 2018). "Genetic counseling among minority populations in the era of precision medicine". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 178 (1): 68–74. doi:10.1002/ajmg.c.31604. PMID 29575517. S2CID 4325950.
Yanes, Tatiane; Sullivan, Anna; Barbaro, Pasquale; Brion, Kristian; Hollway, Georgina; Peake, Jane; McNaughton, Peter (2023-10-01). "Evaluation and pilot testing of a multidisciplinary model of care to mainstream genomic testing for paediatric inborn errors of immunity". European Journal of Human Genetics. 31 (10): 1125–1132. doi:10.1038/s41431-023-01321-z. ISSN 1476-5438. PMC 10545723. PMID 36864115.
Bokkers, Kyra; Vlaming, Michiel; Engelhardt, Ellen G.; Zweemer, Ronald P.; van Oort, Inge M.; Kiemeney, Lambertus A. L. M.; Bleiker, Eveline M. A.; Ausems, Margreet G. E. M. (January 2022). "The Feasibility of Implementing Mainstream Germline Genetic Testing in Routine Cancer Care—A Systematic Review". Cancers. 14 (4): 1059. doi:10.3390/cancers14041059. ISSN 2072-6694. PMC 8870548. PMID 35205807.

elsevier.com

linkinghub.elsevier.com

Ormond, Kelly E.; Abad, Peter James; MacLeod, Rhona; Nishigaki, Masakazu; Wessels, Tina-Marié (2024-08-07). "The global status of genetic counselors in 2023: What has changed in the past 5 years?". Genetics in Medicine Open: 101887. doi:10.1016/j.gimo.2024.101887. hdl:20.500.11850/704802. Retrieved 2024-10-11.

gceducation.org

"Accredited Programs". gceducation.org. Archived from the original on 2018-12-09. Retrieved 2018-10-01.

gcrb.org.uk

"Overseas Applicants". Genetic Counsellor Registration Board. Archived from the original on 2021-04-29. Retrieved 2021-04-29.

geneticalliance.org

"Genetic Alliance Site". Retrieved 29 October 2010.

gotowebinar.com

register.gotowebinar.com

Schwartz, Lisa (2024-10-29). "UTS Webinar: Times are Changing: GC Professional Identity". GoToWebinar. Retrieved 2025-01-13.

govtrack.us

Tauberer J. "H.R. 3235 (116th): Access to Genetic Counselor Services Act of 2019". GovTrack. Civic Impulse, LLC.
Tauberer J. "Access to Genetic Counselor Services Act of 2019 (H.R. 3235)". GovTrack. Civic Impulse, LLC. Retrieved 2019-08-14.

handle.net

hdl.handle.net

Hershberger RE, Givertz MM, Ho CY, Judge DP, Kantor PF, McBride KL, et al. (May 2018). "Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline". Journal of Cardiac Failure. 24 (5): 281–302. doi:10.1016/j.cardfail.2018.03.004. hdl:1805/15853. PMC 9903357. PMID 29567486.
Moldovan R, Pintea S, Austin J (December 2017). "The Efficacy of Genetic Counseling for Psychiatric Disorders: a Meta-Analysis". Journal of Genetic Counseling. 26 (6): 1341–1347. doi:10.1007/s10897-017-0113-8. hdl:2429/68096. PMID 28616830.
Ormond, Kelly E.; Abad, Peter James; MacLeod, Rhona; Nishigaki, Masakazu; Wessels, Tina-Marié (2024-08-07). "The global status of genetic counselors in 2023: What has changed in the past 5 years?". Genetics in Medicine Open: 101887. doi:10.1016/j.gimo.2024.101887. hdl:20.500.11850/704802. Retrieved 2024-10-11.

hgsa.org.au

"GENETIC COUNSELLING IN AUSTRALIA:COST BENEFIT ANALYSIS OF MEDICARE LISTING" (PDF). Human Genetics Society of Australasia. Econisis. 2024-12-02. p. 6. Retrieved 2025-01-16.

hpcsa.co.za

"Home Page – HPCSA". hpcsa.co.za. Retrieved 2018-08-15.

nccn.org

"Clinical Practice Guidelines in Oncology". National Comprehensive Cancer Network (NCCN). Retrieved 2018-09-30.

nhs.uk

"Genetic testing and counselling". nhs.uk. Retrieved 2018-08-16.

nih.gov

pubmed.ncbi.nlm.nih.gov

Patch C, Middleton A (June 2018). "Genetic counselling in the era of genomic medicine". British Medical Bulletin. 126 (1): 27–36. doi:10.1093/bmb/ldy008. PMC 5998955. PMID 29617718.
Resta R, Biesecker BB, Bennett RL, Blum S, Hahn SE, Strecker MN, Williams JL (April 2006). "A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report". Journal of Genetic Counseling. 15 (2): 77–83. doi:10.1007/s10897-005-9014-3. PMID 16761103. S2CID 25809385.
Reed SC (December 1974). "A short history of genetic counseling". Social Biology. 21 (4): 332–9. doi:10.1080/19485565.1974.9988131. PMID 4619717.
Veach PM, Bartels DM, Leroy BS (December 2007). "Coming full circle: a reciprocal-engagement model of genetic counseling practice". Journal of Genetic Counseling. 16 (6): 713–28. doi:10.1007/s10897-007-9113-4. PMID 17934802.
Biesecker B, Austin J, Caleshu C (April 2017). "Response to A Different Vantage Point Commentary: Psychotherapeutic Genetic Counseling, Is it?". Journal of Genetic Counseling. 26 (2): 334–336. doi:10.1007/s10897-016-0025-z. PMC 5383505. PMID 27804046.
Austin J, Semaka A, Hadjipavlou G (December 2014). "Conceptualizing genetic counseling as psychotherapy in the era of genomic medicine". Journal of Genetic Counseling. 23 (6): 903–9. doi:10.1007/s10897-014-9728-1. PMC 4318692. PMID 24841456.
Hodgson JM, Gillam LH, Sahhar MA, Metcalfe SA (February 2010). ""Testing times, challenging choices": an Australian study of prenatal genetic counseling". Journal of Genetic Counseling. 19 (1): 22–37. doi:10.1007/s10897-009-9248-6. PMID 19798554. S2CID 10085887.
Dolan SM (August 2009). "Prenatal genetic testing". Pediatric Annals. 38 (8): 426–30. doi:10.3928/00904481-20090723-05. PMID 19711880.
Madlensky L, Trepanier AM, Cragun D, Lerner B, Shannon KM, Zierhut H (June 2017). "A Rapid Systematic Review of Outcomes Studies in Genetic Counseling". Journal of Genetic Counseling. 26 (3): 361–378. doi:10.1007/s10897-017-0067-x. PMID 28168332.
Corpas M (June 2012). "A family experience of personal genomics". Journal of Genetic Counseling. 21 (3): 386–91. doi:10.1007/s10897-011-9473-7. PMID 22223063. S2CID 10845045.
Gilchrist DM (October 2002). "Medical genetics: 3. An approach to the adult with a genetic disorder". CMAJ. 167 (9): 1021–9. doi:10.1007/s10897-011-9473-7. PMC 134180. PMID 12403743.
Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C, et al. (December 2013). "HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013". Heart Rhythm. 10 (12): 1932–63. doi:10.1016/j.hrthm.2013.05.014. PMID 24011539.
Hershberger RE, Givertz MM, Ho CY, Judge DP, Kantor PF, McBride KL, et al. (May 2018). "Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline". Journal of Cardiac Failure. 24 (5): 281–302. doi:10.1016/j.cardfail.2018.03.004. hdl:1805/15853. PMC 9903357. PMID 29567486.
Gersh BJ, Maron BJ, Bonow RO, Dearani JA, Fifer MA, Link MS, et al. (December 2011). "2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines". Circulation. 124 (24): e783-831. doi:10.1161/CIR.0b013e318223e2bd. PMID 22068434.
Elliott PM, Anastasakis A, Borger MA, Borggrefe M, Cecchi F, Charron P, et al. (October 2014). "2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC)". European Heart Journal. 35 (39): 2733–79. doi:10.1093/eurheartj/ehu284. PMID 25173338.
Goldberg AC, Hopkins PN, Toth PP, Ballantyne CM, Rader DJ, Robinson JG, et al. (June 2011). "Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia". Journal of Clinical Lipidology. 5 (3 Suppl): S1-8. doi:10.1016/j.jacl.2011.04.003. PMID 21600525.
Gidding SS, Champagne MA, de Ferranti SD, Defesche J, Ito MK, Knowles JW, et al. (December 2015). "The Agenda for Familial Hypercholesterolemia: A Scientific Statement From the American Heart Association". Circulation. 132 (22): 2167–92. doi:10.1161/CIR.0000000000000297. PMID 26510694. S2CID 9980924.
Couch FJ, Hart SN, Sharma P, Toland AE, Wang X, Miron P, et al. (February 2015). "Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer". Journal of Clinical Oncology. 33 (4): 304–11. doi:10.1200/jco.2014.57.1414. PMC 4302212. PMID 25452441.
Pritchard CC, Mateo J, Walsh MF, De Sarkar N, Abida W, Beltran H, et al. (August 2016). "Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer". The New England Journal of Medicine. 375 (5): 443–53. doi:10.1056/nejmoa1603144. PMC 4986616. PMID 27433846.
Holter S, Borgida A, Dodd A, Grant R, Semotiuk K, Hedley D, et al. (October 2015). "Germline BRCA Mutations in a Large Clinic-Based Cohort of Patients With Pancreatic Adenocarcinoma". Journal of Clinical Oncology. 33 (28): 3124–9. doi:10.1200/jco.2014.59.7401. PMID 25940717.
Varley JM, McGown G, Thorncroft M, James LA, Margison GP, Forster G, et al. (October 1999). "Are there low-penetrance TP53 Alleles? evidence from childhood adrenocortical tumors". American Journal of Human Genetics. 65 (4): 995–1006. doi:10.1086/302575. PMC 1288270. PMID 10486318.
Lenders JW, Duh QY, Eisenhofer G, Gimenez-Roqueplo AP, Grebe SK, Murad MH, et al. (June 2014). "Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline". The Journal of Clinical Endocrinology and Metabolism. 99 (6): 1915–42. doi:10.1210/jc.2014-1498. PMID 24893135.
Walsh T, Mandell JB, Norquist BM, Casadei S, Gulsuner S, Lee MK, King MC (December 2017). "Genetic Predisposition to Breast Cancer Due to Mutations Other Than BRCA1 and BRCA2 Founder Alleles Among Ashkenazi Jewish Women". JAMA Oncology. 3 (12): 1647–1653. doi:10.1001/jamaoncol.2017.1996. PMC 5824270. PMID 28727877.
Raymond VM, Gray SW, Roychowdhury S, Joffe S, Chinnaiyan AM, Parsons DW, Plon SE (April 2016). "Germline Findings in Tumor-Only Sequencing: Points to Consider for Clinicians and Laboratories". Journal of the National Cancer Institute. 108 (4): djv351. doi:10.1093/jnci/djv351. PMC 4849259. PMID 26590952.
Radtke HB, Sebold CD, Allison C, Haidle JL, Schneider G (August 2007). "Neurofibromatosis type 1 in genetic counseling practice: recommendations of the National Society of Genetic Counselors". Journal of Genetic Counseling. 16 (4): 387–407. doi:10.1007/s10897-007-9101-8. PMC 6338721. PMID 17636453.
Pong AW, Pal DK, Chung WK (May 2011). "Developments in molecular genetic diagnostics: an update for the pediatric epilepsy specialist". Pediatric Neurology. 44 (5): 317–27. doi:10.1016/j.pediatrneurol.2011.01.017. PMID 21481738.
Helbig I, Scheffer IE, Mulley JC, Berkovic SF (March 2008). "Navigating the channels and beyond: unravelling the genetics of the epilepsies". The Lancet. Neurology. 7 (3): 231–45. doi:10.1016/S1474-4422(08)70039-5. PMID 18275925. S2CID 23243066.
Scheffer IE (April 2014). "Epilepsy genetics revolutionizes clinical practice". Neuropediatrics. 45 (2): 70–4. doi:10.1055/s-0034-1371508. PMID 24615646.
Renton AE, Chiò A, Traynor BJ (January 2014). "State of play in amyotrophic lateral sclerosis genetics". Nature Neuroscience. 17 (1): 17–23. doi:10.1038/nn.3584. PMC 4544832. PMID 24369373.
Benatar M, Stanislaw C, Reyes E, Hussain S, Cooley A, Fernandez MC, et al. (June 2016). "Presymptomatic ALS genetic counseling and testing: Experience and recommendations". Neurology. 86 (24): 2295–302. doi:10.1212/WNL.0000000000002773. PMC 4909562. PMID 27194384.
Miles JH (April 2011). "Autism spectrum disorders--a genetics review". Genetics in Medicine. 13 (4): 278–94. doi:10.1097/GIM.0b013e3181ff67ba. PMID 21358411.
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, et al. (May 2010). "Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies". American Journal of Human Genetics. 86 (5): 749–64. doi:10.1016/j.ajhg.2010.04.006. PMC 2869000. PMID 20466091.
Campion D, Dumanchin C, Hannequin D, Dubois B, Belliard S, Puel M, et al. (September 1999). "Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum". American Journal of Human Genetics. 65 (3): 664–70. doi:10.1086/302553. PMC 1377972. PMID 10441572.
Goldman JS, Hahn SE, Catania JW, LaRusse-Eckert S, Butson MB, Rumbaugh M, et al. (June 2011). "Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors". Genetics in Medicine. 13 (6): 597–605. doi:10.1097/GIM.0b013e31821d69b8. PMC 3326653. PMID 21577118.
Crozier S, Robertson N, Dale M (February 2015). "The psychological impact of predictive genetic testing for Huntington's disease: a systematic review of the literature". Journal of Genetic Counseling. 24 (1): 29–39. doi:10.1007/s10897-014-9755-y. PMID 25236481. S2CID 18140209.
Went L (January 1990). "Ethical issues policy statement on Huntington's disease molecular genetics predictive test. International Huntington Association. World Federation of Neurology". Journal of Medical Genetics. 27 (1): 34–8. doi:10.1136/jmg.27.1.34. PMC 1016877. PMID 2137881.
Singleton AB, Farrer MJ, Bonifati V (January 2013). "The genetics of Parkinson's disease: progress and therapeutic implications". Movement Disorders. 28 (1): 14–23. doi:10.1002/mds.25249. PMC 3578399. PMID 23389780.
Trinh J, Farrer M (August 2013). "Advances in the genetics of Parkinson disease". Nature Reviews. Neurology. 9 (8): 445–54. doi:10.1038/nrneurol.2013.132. PMID 23857047. S2CID 31028719.
Pletcher BA, Toriello HV, Noblin SJ, Seaver LH, Driscoll DA, Bennett RL, Gross SJ (June 2007). "Indications for genetic referral: a guide for healthcare providers". Genetics in Medicine. 9 (6): 385–9. doi:10.1097/GIM.0b013e318064e70c. PMC 3110962. PMID 17575505.
American College of Obstetricians Gynecologists' Committee on Practice Bulletins—Obstetrics; Society for Maternal–Fetal Medicine (May 2016). "Practice Bulletin No. 162: Prenatal Diagnostic Testing for Genetic Disorders". Obstetrics and Gynecology. 127 (5): e108 – e122. doi:10.1097/AOG.0000000000001405. PMID 26938573. S2CID 25791506.
Benn P, Borrell A, Chiu RW, Cuckle H, Dugoff L, Faas B, et al. (August 2015). "Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis". Prenatal Diagnosis. 35 (8): 725–34. doi:10.1002/pd.4608. PMID 25970088. S2CID 23477914.
Gregg AR, Skotko BG, Benkendorf JL, Monaghan KG, Bajaj K, Best RG, et al. (October 2016). "Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics". Genetics in Medicine. 18 (10): 1056–65. doi:10.1038/gim.2016.97. PMID 27467454.
Wilson KL, Czerwinski JL, Hoskovec JM, Noblin SJ, Sullivan CM, Harbison A, et al. (February 2013). "NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy". Journal of Genetic Counseling. 22 (1): 4–15. doi:10.1007/s10897-012-9545-3. PMID 23179172. S2CID 13126623.
Committee On Practice Bulletins—Obstetrics; Committee on Genetics (May 2016). "Practice Bulletin No. 163: Screening for Fetal Aneuploidy". Obstetrics and Gynecology. 127 (5): e123 – e137. doi:10.1097/AOG.0000000000001406. PMID 26938574. S2CID 40095460.
Dugoff L, Norton ME, Kuller JA (October 2016). "The use of chromosomal microarray for prenatal diagnosis". American Journal of Obstetrics and Gynecology. 215 (4): B2-9. doi:10.1016/j.ajog.2016.07.016. PMID 27427470.
International Society for Prenatal Diagnosis; Society for Maternal Fetal Medicine (January 2018). "Joint Position Statement from the International Society for Prenatal Diagnosis (ISPD), the Society for Maternal Fetal Medicine (SMFM), and the Perinatal Quality Foundation (PQF) on the use of genome-wide sequencing for fetal diagnosis". Prenatal Diagnosis. 38 (1): 6–9. doi:10.1002/pd.5195. PMID 29315690.
Grody WW, Thompson BH, Gregg AR, Bean LH, Monaghan KG, Schneider A, Lebo RV (June 2013). "ACMG position statement on prenatal/preconception expanded carrier screening". Genetics in Medicine. 15 (6): 482–3. doi:10.1038/gim.2013.47. PMID 23619275.
"Committee Opinion No. 640: Cell-Free DNA Screening For Fetal Aneuploidy". Obstetrics and Gynecology. 126 (3): e31 – e37. September 2015. doi:10.1097/AOG.0000000000001051. PMID 26287791. S2CID 10876600.
Dondorp W, de Wert G, Bombard Y, Bianchi DW, Bergmann C, Borry P, et al. (April 2015). "Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations". European Journal of Human Genetics. doi:10.1038/ejhg.2015.56. PMID 25828867.
"Committee Opinion No. 690 Summary: Carrier Screening in the Age of Genomic Medicine". Obstetrics and Gynecology. 129 (3): 595–596. March 2017. doi:10.1097/AOG.0000000000001947. PMID 28225420.
Bennett RL, Motulsky AG, Bittles A, Hudgins L, Uhrich S, Doyle DL, et al. (April 2002). "Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic Counselors". Journal of Genetic Counseling. 11 (2): 97–119. doi:10.1023/A:1014593404915. PMID 26141656. S2CID 23922750.
Rothwell E, Johnson E, Mathiesen A, Golden K, Metcalf A, Rose NC, Botkin JR (August 2017). "Experiences among Women with Positive Prenatal Expanded Carrier Screening Results". Journal of Genetic Counseling. 26 (4): 690–696. doi:10.1007/s10897-016-0037-8. PMC 5432405. PMID 27796679.
Stefansdottir V, Skirton H, Jonasson K, Hardardottir H, Jonsson JJ (July 2010). "Effects of knowledge, education, and experience on acceptance of first trimester screening for chromosomal anomalies". Acta Obstetricia et Gynecologica Scandinavica. 89 (7): 931–8. doi:10.3109/00016341003686073. PMID 20235896. S2CID 22380002.
Muthuswamy, Vasantha (October 2011). "Ethical issues in genetic counselling with special reference to haemoglobinopathies". The Indian Journal of Medical Research. 134 (4): 547–551. ISSN 0971-5916. PMC 3237255. PMID 22089619.
Giegling I, Hosak L, Mössner R, Serretti A, Bellivier F, Claes S, et al. (October 2017). "Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics" (PDF). The World Journal of Biological Psychiatry. 18 (7): 492–505. doi:10.1080/15622975.2016.1268715. PMID 28112043. S2CID 4662474.
Inglis A, Morris E, Austin J (January 2017). "Prenatal genetic counselling for psychiatric disorders". Prenatal Diagnosis. 37 (1): 6–13. doi:10.1002/pd.4878. PMC 5247258. PMID 27466037.
Ryan J, Virani A, Austin JC (June 2015). "Ethical issues associated with genetic counseling in the context of adolescent psychiatry". Applied & Translational Genomics. 5: 23–9. doi:10.1016/j.atg.2015.06.001. PMC 4745399. PMID 26937355.
Demkow U, Wolańczyk T (June 2017). "Genetic tests in major psychiatric disorders-integrating molecular medicine with clinical psychiatry-why is it so difficult?". Translational Psychiatry. 7 (6): e1151. doi:10.1038/tp.2017.106. PMC 5537634. PMID 28608853.
Moldovan R, Pintea S, Austin J (December 2017). "The Efficacy of Genetic Counseling for Psychiatric Disorders: a Meta-Analysis". Journal of Genetic Counseling. 26 (6): 1341–1347. doi:10.1007/s10897-017-0113-8. hdl:2429/68096. PMID 28616830.
Tsuang MT (December 1978). "Genetic counseling for psychiatric patients and their families". The American Journal of Psychiatry. 135 (12): 1465–75. doi:10.1176/ajp.135.12.1465. PMID 717559.
Abacan M, Alsubaie L, Barlow-Stewart K, Caanen B, Cordier C, Courtney E, et al. (February 2019). "The Global State of the Genetic Counseling Profession". European Journal of Human Genetics. 27 (2): 183–197. doi:10.1038/s41431-018-0252-x. PMC 6336871. PMID 30291341.
Zhao X, Wang P, Tao X, Zhong N (July 2013). "Genetic services and testing in China". Journal of Community Genetics. 4 (3): 379–90. doi:10.1007/s12687-013-0144-2. PMC 3739851. PMID 23595912.
Li J, Xu T, Yashar BM (September 2015). "Genetics educational needs in China: physicians' experience and knowledge of genetic testing". Genetics in Medicine. 17 (9): 757–60. doi:10.1038/gim.2014.182. PMID 25503494. S2CID 21625217.
Kromberg JG, Wessels TM, Krause A (December 2013). "Roles of genetic counselors in South Africa". Journal of Genetic Counseling. 22 (6): 753–61. doi:10.1007/s10897-013-9606-2. PMID 23723047. S2CID 18335348.
Ormond KE, Laurino MY, Barlow-Stewart K, Wessels TM, Macaulay S, Austin J, Middleton A (March 2018). "Genetic counseling globally: Where are we now?". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 178 (1): 98–107. doi:10.1002/ajmg.c.31607. PMC 5947883. PMID 29575600.
Abacan M, Alsubaie L, Barlow-Stewart K, Caanen B, Cordier C, Courtney E, et al. (February 2019). "The Global State of the Genetic Counseling Profession". European Journal of Human Genetics. 27 (2): 183–197. doi:10.1038/s41431-018-0252-x. PMC 6336871. PMID 30291341.
Isbister, Joanne; Sexton, Adrienne; Forrest, Laura E.; James, Paul; Dowty, James; Taylor, Jessica; Austin, Jehannine; Winship, Ingrid (April 2023). "Psychiatric genetic counseling: A survey of Australian genetic counselors' practice and attitudes". Journal of Genetic Counseling. 32 (2): 495–502. doi:10.1002/jgc4.1659. ISSN 1059-7700. PMID 36480151. S2CID 254478392.
Balobaid A, Qari A, Al-Zaidan H (March 2016). "Genetic counselors' scope of practice and challenges in genetic counseling services in Saudi Arabia". International Journal of Pediatrics & Adolescent Medicine. 3 (1): 1–6. doi:10.1016/j.ijpam.2015.12.002. PMC 6372413. PMID 30805460.
Gallagher TM, Bucciarelli M, Kavalukas SL, Baker MJ, Saunders BD (September 2017). "Attitudes toward genetic counseling and testing in patients with inherited endocrinopathies". Endocrine Practice. 23 (9): 1039–1044. doi:10.4158/EP171875.OR. PMID 28613942.
Haga SB, Barry WT, Mills R, Ginsburg GS, Svetkey L, Sullivan J, Willard HF (April 2013). "Public knowledge of and attitudes toward genetics and genetic testing". Genetic Testing and Molecular Biomarkers. 17 (4): 327–35. doi:10.1089/gtmb.2012.0350. PMC 3609633. PMID 23406207.
Scuffham TM, McInerny-Leo A, Ng SK, Mellick G (April 2014). "Knowledge and attitudes towards genetic testing in those affected with Parkinson's disease". Journal of Community Genetics. 5 (2): 167–77. doi:10.1007/s12687-013-0168-7. PMC 3955457. PMID 24018619.
Singer E, Couper MP, Raghunathan TE, Van Hoewyk J, Antonucci TC (Fall 2008). "Trends in U.S. Attitudes Toward Genetic Testing, 1990-2004". Public Opinion Quarterly. 72 (3): 446–458. doi:10.1093/poq/nfn033. PMC 3045776. PMID 22476359.
Halbert CH, Harrison BW (March 2018). "Genetic counseling among minority populations in the era of precision medicine". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 178 (1): 68–74. doi:10.1002/ajmg.c.31604. PMID 29575517. S2CID 4325950.
Yanes, Tatiane; Sullivan, Anna; Barbaro, Pasquale; Brion, Kristian; Hollway, Georgina; Peake, Jane; McNaughton, Peter (2023-10-01). "Evaluation and pilot testing of a multidisciplinary model of care to mainstream genomic testing for paediatric inborn errors of immunity". European Journal of Human Genetics. 31 (10): 1125–1132. doi:10.1038/s41431-023-01321-z. ISSN 1476-5438. PMC 10545723. PMID 36864115.
Bokkers, Kyra; Vlaming, Michiel; Engelhardt, Ellen G.; Zweemer, Ronald P.; van Oort, Inge M.; Kiemeney, Lambertus A. L. M.; Bleiker, Eveline M. A.; Ausems, Margreet G. E. M. (January 2022). "The Feasibility of Implementing Mainstream Germline Genetic Testing in Routine Cancer Care—A Systematic Review". Cancers. 14 (4): 1059. doi:10.3390/cancers14041059. ISSN 2072-6694. PMC 8870548. PMID 35205807.

ncbi.nlm.nih.gov

Patch C, Middleton A (June 2018). "Genetic counselling in the era of genomic medicine". British Medical Bulletin. 126 (1): 27–36. doi:10.1093/bmb/ldy008. PMC 5998955. PMID 29617718.
Biesecker B, Austin J, Caleshu C (April 2017). "Response to A Different Vantage Point Commentary: Psychotherapeutic Genetic Counseling, Is it?". Journal of Genetic Counseling. 26 (2): 334–336. doi:10.1007/s10897-016-0025-z. PMC 5383505. PMID 27804046.
Austin J, Semaka A, Hadjipavlou G (December 2014). "Conceptualizing genetic counseling as psychotherapy in the era of genomic medicine". Journal of Genetic Counseling. 23 (6): 903–9. doi:10.1007/s10897-014-9728-1. PMC 4318692. PMID 24841456.
Gilchrist DM (October 2002). "Medical genetics: 3. An approach to the adult with a genetic disorder". CMAJ. 167 (9): 1021–9. doi:10.1007/s10897-011-9473-7. PMC 134180. PMID 12403743.
Hershberger RE, Givertz MM, Ho CY, Judge DP, Kantor PF, McBride KL, et al. (May 2018). "Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline". Journal of Cardiac Failure. 24 (5): 281–302. doi:10.1016/j.cardfail.2018.03.004. hdl:1805/15853. PMC 9903357. PMID 29567486.
Couch FJ, Hart SN, Sharma P, Toland AE, Wang X, Miron P, et al. (February 2015). "Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer". Journal of Clinical Oncology. 33 (4): 304–11. doi:10.1200/jco.2014.57.1414. PMC 4302212. PMID 25452441.
Pritchard CC, Mateo J, Walsh MF, De Sarkar N, Abida W, Beltran H, et al. (August 2016). "Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer". The New England Journal of Medicine. 375 (5): 443–53. doi:10.1056/nejmoa1603144. PMC 4986616. PMID 27433846.
Varley JM, McGown G, Thorncroft M, James LA, Margison GP, Forster G, et al. (October 1999). "Are there low-penetrance TP53 Alleles? evidence from childhood adrenocortical tumors". American Journal of Human Genetics. 65 (4): 995–1006. doi:10.1086/302575. PMC 1288270. PMID 10486318.
Walsh T, Mandell JB, Norquist BM, Casadei S, Gulsuner S, Lee MK, King MC (December 2017). "Genetic Predisposition to Breast Cancer Due to Mutations Other Than BRCA1 and BRCA2 Founder Alleles Among Ashkenazi Jewish Women". JAMA Oncology. 3 (12): 1647–1653. doi:10.1001/jamaoncol.2017.1996. PMC 5824270. PMID 28727877.
Raymond VM, Gray SW, Roychowdhury S, Joffe S, Chinnaiyan AM, Parsons DW, Plon SE (April 2016). "Germline Findings in Tumor-Only Sequencing: Points to Consider for Clinicians and Laboratories". Journal of the National Cancer Institute. 108 (4): djv351. doi:10.1093/jnci/djv351. PMC 4849259. PMID 26590952.
Radtke HB, Sebold CD, Allison C, Haidle JL, Schneider G (August 2007). "Neurofibromatosis type 1 in genetic counseling practice: recommendations of the National Society of Genetic Counselors". Journal of Genetic Counseling. 16 (4): 387–407. doi:10.1007/s10897-007-9101-8. PMC 6338721. PMID 17636453.
Renton AE, Chiò A, Traynor BJ (January 2014). "State of play in amyotrophic lateral sclerosis genetics". Nature Neuroscience. 17 (1): 17–23. doi:10.1038/nn.3584. PMC 4544832. PMID 24369373.
Benatar M, Stanislaw C, Reyes E, Hussain S, Cooley A, Fernandez MC, et al. (June 2016). "Presymptomatic ALS genetic counseling and testing: Experience and recommendations". Neurology. 86 (24): 2295–302. doi:10.1212/WNL.0000000000002773. PMC 4909562. PMID 27194384.
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, et al. (May 2010). "Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies". American Journal of Human Genetics. 86 (5): 749–64. doi:10.1016/j.ajhg.2010.04.006. PMC 2869000. PMID 20466091.
Campion D, Dumanchin C, Hannequin D, Dubois B, Belliard S, Puel M, et al. (September 1999). "Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum". American Journal of Human Genetics. 65 (3): 664–70. doi:10.1086/302553. PMC 1377972. PMID 10441572.
Goldman JS, Hahn SE, Catania JW, LaRusse-Eckert S, Butson MB, Rumbaugh M, et al. (June 2011). "Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors". Genetics in Medicine. 13 (6): 597–605. doi:10.1097/GIM.0b013e31821d69b8. PMC 3326653. PMID 21577118.
Went L (January 1990). "Ethical issues policy statement on Huntington's disease molecular genetics predictive test. International Huntington Association. World Federation of Neurology". Journal of Medical Genetics. 27 (1): 34–8. doi:10.1136/jmg.27.1.34. PMC 1016877. PMID 2137881.
Singleton AB, Farrer MJ, Bonifati V (January 2013). "The genetics of Parkinson's disease: progress and therapeutic implications". Movement Disorders. 28 (1): 14–23. doi:10.1002/mds.25249. PMC 3578399. PMID 23389780.
Pletcher BA, Toriello HV, Noblin SJ, Seaver LH, Driscoll DA, Bennett RL, Gross SJ (June 2007). "Indications for genetic referral: a guide for healthcare providers". Genetics in Medicine. 9 (6): 385–9. doi:10.1097/GIM.0b013e318064e70c. PMC 3110962. PMID 17575505.
Rothwell E, Johnson E, Mathiesen A, Golden K, Metcalf A, Rose NC, Botkin JR (August 2017). "Experiences among Women with Positive Prenatal Expanded Carrier Screening Results". Journal of Genetic Counseling. 26 (4): 690–696. doi:10.1007/s10897-016-0037-8. PMC 5432405. PMID 27796679.
Muthuswamy, Vasantha (October 2011). "Ethical issues in genetic counselling with special reference to haemoglobinopathies". The Indian Journal of Medical Research. 134 (4): 547–551. ISSN 0971-5916. PMC 3237255. PMID 22089619.
Inglis A, Morris E, Austin J (January 2017). "Prenatal genetic counselling for psychiatric disorders". Prenatal Diagnosis. 37 (1): 6–13. doi:10.1002/pd.4878. PMC 5247258. PMID 27466037.
Ryan J, Virani A, Austin JC (June 2015). "Ethical issues associated with genetic counseling in the context of adolescent psychiatry". Applied & Translational Genomics. 5: 23–9. doi:10.1016/j.atg.2015.06.001. PMC 4745399. PMID 26937355.
Demkow U, Wolańczyk T (June 2017). "Genetic tests in major psychiatric disorders-integrating molecular medicine with clinical psychiatry-why is it so difficult?". Translational Psychiatry. 7 (6): e1151. doi:10.1038/tp.2017.106. PMC 5537634. PMID 28608853.
Abacan M, Alsubaie L, Barlow-Stewart K, Caanen B, Cordier C, Courtney E, et al. (February 2019). "The Global State of the Genetic Counseling Profession". European Journal of Human Genetics. 27 (2): 183–197. doi:10.1038/s41431-018-0252-x. PMC 6336871. PMID 30291341.
Zhao X, Wang P, Tao X, Zhong N (July 2013). "Genetic services and testing in China". Journal of Community Genetics. 4 (3): 379–90. doi:10.1007/s12687-013-0144-2. PMC 3739851. PMID 23595912.
Ormond KE, Laurino MY, Barlow-Stewart K, Wessels TM, Macaulay S, Austin J, Middleton A (March 2018). "Genetic counseling globally: Where are we now?". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 178 (1): 98–107. doi:10.1002/ajmg.c.31607. PMC 5947883. PMID 29575600.
Abacan M, Alsubaie L, Barlow-Stewart K, Caanen B, Cordier C, Courtney E, et al. (February 2019). "The Global State of the Genetic Counseling Profession". European Journal of Human Genetics. 27 (2): 183–197. doi:10.1038/s41431-018-0252-x. PMC 6336871. PMID 30291341.
Kanga-Parabia, Anaita; Mitchell, Lucas; Smyth, Renee; Kapoor, Trisha; Duggal, Jaitika; Pearn, Amy; Williams, Rachel; Courtney, Eliza; Edwards, Emma; Bowman, Michelle; Belekar, Mithila; Nisselle, Amy; Pearn, Amy; Kanga-Parabia, Anaita; Lundie, Ben (2024-05-07). "Genetic counseling workforce diversity, inclusion, and capacity in Australia and New Zealand". Genetics in Medicine Open: 101848. doi:10.1016/j.gimo.2024.101848. ISSN 2949-7744. PMC 11658314.
Balobaid A, Qari A, Al-Zaidan H (March 2016). "Genetic counselors' scope of practice and challenges in genetic counseling services in Saudi Arabia". International Journal of Pediatrics & Adolescent Medicine. 3 (1): 1–6. doi:10.1016/j.ijpam.2015.12.002. PMC 6372413. PMID 30805460.
Haga SB, Barry WT, Mills R, Ginsburg GS, Svetkey L, Sullivan J, Willard HF (April 2013). "Public knowledge of and attitudes toward genetics and genetic testing". Genetic Testing and Molecular Biomarkers. 17 (4): 327–35. doi:10.1089/gtmb.2012.0350. PMC 3609633. PMID 23406207.
Scuffham TM, McInerny-Leo A, Ng SK, Mellick G (April 2014). "Knowledge and attitudes towards genetic testing in those affected with Parkinson's disease". Journal of Community Genetics. 5 (2): 167–77. doi:10.1007/s12687-013-0168-7. PMC 3955457. PMID 24018619.
Singer E, Couper MP, Raghunathan TE, Van Hoewyk J, Antonucci TC (Fall 2008). "Trends in U.S. Attitudes Toward Genetic Testing, 1990-2004". Public Opinion Quarterly. 72 (3): 446–458. doi:10.1093/poq/nfn033. PMC 3045776. PMID 22476359.
Yanes, Tatiane; Sullivan, Anna; Barbaro, Pasquale; Brion, Kristian; Hollway, Georgina; Peake, Jane; McNaughton, Peter (2023-10-01). "Evaluation and pilot testing of a multidisciplinary model of care to mainstream genomic testing for paediatric inborn errors of immunity". European Journal of Human Genetics. 31 (10): 1125–1132. doi:10.1038/s41431-023-01321-z. ISSN 1476-5438. PMC 10545723. PMID 36864115.
Bokkers, Kyra; Vlaming, Michiel; Engelhardt, Ellen G.; Zweemer, Ronald P.; van Oort, Inge M.; Kiemeney, Lambertus A. L. M.; Bleiker, Eveline M. A.; Ausems, Margreet G. E. M. (January 2022). "The Feasibility of Implementing Mainstream Germline Genetic Testing in Routine Cancer Care—A Systematic Review". Cancers. 14 (4): 1059. doi:10.3390/cancers14041059. ISSN 2072-6694. PMC 8870548. PMID 35205807.

npr.org

Stallings E (27 July 2019). "Genetic Counselors Of Color Tackle Racial, Ethnic Disparities In Health Care". NPR.org. National Public Radio. Retrieved 2021-02-12.

nsgc.org

"Interested in Becoming a Genetic Counselor". nsgc.org. Retrieved 2018-01-30.
"States Issuing Licenses for Genetic Counselors". National Society of Genetic Counselors. Archived from the original on 16 July 2018. Retrieved 3 October 2018.
"NSGC Blog". National Society of Genetic Counselors. Archived from the original on 15 August 2019. Retrieved 15 August 2019.
"Blogs: Black History Month: Bearing the torch of equity as an African-American genetic counselor and scientist". nsgc.org. National Society of Genetic Counselors. Archived from the original on 2021-01-20. Retrieved 2021-02-12.

nysgeneticcounselors.org

"NYS Genetic Counseling Information Resource". nysgeneticcounselors.org. Retrieved 2018-09-12.

sarahlawrence.edu

"History of the Joan H. Marks Graduate Program in Human Genetics at Sarah Lawrence College". Retrieved 2018-09-12.

sashg.org

"Genetic Counselling South Africa". sashg.org. Archived from the original on 2018-08-16. Retrieved 2018-08-15.
"Southern African Society for Human Genetics (SASHG)". SASHG.org. Retrieved 2018-08-15.

semanticscholar.org

api.semanticscholar.org

Resta R, Biesecker BB, Bennett RL, Blum S, Hahn SE, Strecker MN, Williams JL (April 2006). "A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report". Journal of Genetic Counseling. 15 (2): 77–83. doi:10.1007/s10897-005-9014-3. PMID 16761103. S2CID 25809385.
Veach PM, LeRoy BS, Bartels DM (2003). Facilitating the Genetic Counselling Process. Springer. doi:10.1007/978-3-319-74799-6. ISBN 978-3-319-74798-9. S2CID 13808432.
Kessler S (May 1984). "Book Review: A Genetic Counseling CasebookA Genetic Counseling Casebook. Edited by Gordon ApplebaumEleanor and FiresteinStephen K.New York: Free Press, 1983. 291 pp.$19.95". Social Casework. 65 (5): 314–316. doi:10.1177/104438948406500509. S2CID 80622038.
Hodgson JM, Gillam LH, Sahhar MA, Metcalfe SA (February 2010). ""Testing times, challenging choices": an Australian study of prenatal genetic counseling". Journal of Genetic Counseling. 19 (1): 22–37. doi:10.1007/s10897-009-9248-6. PMID 19798554. S2CID 10085887.
Corpas M (June 2012). "A family experience of personal genomics". Journal of Genetic Counseling. 21 (3): 386–91. doi:10.1007/s10897-011-9473-7. PMID 22223063. S2CID 10845045.
Gidding SS, Champagne MA, de Ferranti SD, Defesche J, Ito MK, Knowles JW, et al. (December 2015). "The Agenda for Familial Hypercholesterolemia: A Scientific Statement From the American Heart Association". Circulation. 132 (22): 2167–92. doi:10.1161/CIR.0000000000000297. PMID 26510694. S2CID 9980924.
Helbig I, Scheffer IE, Mulley JC, Berkovic SF (March 2008). "Navigating the channels and beyond: unravelling the genetics of the epilepsies". The Lancet. Neurology. 7 (3): 231–45. doi:10.1016/S1474-4422(08)70039-5. PMID 18275925. S2CID 23243066.
Crozier S, Robertson N, Dale M (February 2015). "The psychological impact of predictive genetic testing for Huntington's disease: a systematic review of the literature". Journal of Genetic Counseling. 24 (1): 29–39. doi:10.1007/s10897-014-9755-y. PMID 25236481. S2CID 18140209.
Trinh J, Farrer M (August 2013). "Advances in the genetics of Parkinson disease". Nature Reviews. Neurology. 9 (8): 445–54. doi:10.1038/nrneurol.2013.132. PMID 23857047. S2CID 31028719.
Macdonald F (1 November 2008). "Practice of prenatal diagnosis in the UK". Clinical Risk. 14 (6): 218–221. doi:10.1258/cr.2008.080062. S2CID 58245546.
American College of Obstetricians Gynecologists' Committee on Practice Bulletins—Obstetrics; Society for Maternal–Fetal Medicine (May 2016). "Practice Bulletin No. 162: Prenatal Diagnostic Testing for Genetic Disorders". Obstetrics and Gynecology. 127 (5): e108 – e122. doi:10.1097/AOG.0000000000001405. PMID 26938573. S2CID 25791506.
Benn P, Borrell A, Chiu RW, Cuckle H, Dugoff L, Faas B, et al. (August 2015). "Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis". Prenatal Diagnosis. 35 (8): 725–34. doi:10.1002/pd.4608. PMID 25970088. S2CID 23477914.
Wilson KL, Czerwinski JL, Hoskovec JM, Noblin SJ, Sullivan CM, Harbison A, et al. (February 2013). "NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy". Journal of Genetic Counseling. 22 (1): 4–15. doi:10.1007/s10897-012-9545-3. PMID 23179172. S2CID 13126623.
Committee On Practice Bulletins—Obstetrics; Committee on Genetics (May 2016). "Practice Bulletin No. 163: Screening for Fetal Aneuploidy". Obstetrics and Gynecology. 127 (5): e123 – e137. doi:10.1097/AOG.0000000000001406. PMID 26938574. S2CID 40095460.
"Committee Opinion No. 640: Cell-Free DNA Screening For Fetal Aneuploidy". Obstetrics and Gynecology. 126 (3): e31 – e37. September 2015. doi:10.1097/AOG.0000000000001051. PMID 26287791. S2CID 10876600.
Bennett RL, Motulsky AG, Bittles A, Hudgins L, Uhrich S, Doyle DL, et al. (April 2002). "Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic Counselors". Journal of Genetic Counseling. 11 (2): 97–119. doi:10.1023/A:1014593404915. PMID 26141656. S2CID 23922750.
Stefansdottir V, Skirton H, Jonasson K, Hardardottir H, Jonsson JJ (July 2010). "Effects of knowledge, education, and experience on acceptance of first trimester screening for chromosomal anomalies". Acta Obstetricia et Gynecologica Scandinavica. 89 (7): 931–8. doi:10.3109/00016341003686073. PMID 20235896. S2CID 22380002.
Giegling I, Hosak L, Mössner R, Serretti A, Bellivier F, Claes S, et al. (October 2017). "Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics" (PDF). The World Journal of Biological Psychiatry. 18 (7): 492–505. doi:10.1080/15622975.2016.1268715. PMID 28112043. S2CID 4662474.
Li J, Xu T, Yashar BM (September 2015). "Genetics educational needs in China: physicians' experience and knowledge of genetic testing". Genetics in Medicine. 17 (9): 757–60. doi:10.1038/gim.2014.182. PMID 25503494. S2CID 21625217.
Kromberg JG, Wessels TM, Krause A (December 2013). "Roles of genetic counselors in South Africa". Journal of Genetic Counseling. 22 (6): 753–61. doi:10.1007/s10897-013-9606-2. PMID 23723047. S2CID 18335348.
Isbister, Joanne; Sexton, Adrienne; Forrest, Laura E.; James, Paul; Dowty, James; Taylor, Jessica; Austin, Jehannine; Winship, Ingrid (April 2023). "Psychiatric genetic counseling: A survey of Australian genetic counselors' practice and attitudes". Journal of Genetic Counseling. 32 (2): 495–502. doi:10.1002/jgc4.1659. ISSN 1059-7700. PMID 36480151. S2CID 254478392.
Halbert CH, Harrison BW (March 2018). "Genetic counseling among minority populations in the era of precision medicine". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 178 (1): 68–74. doi:10.1002/ajmg.c.31604. PMID 29575517. S2CID 4325950.

springer.com

Veach PM, LeRoy BS, Bartels DM (2003). Facilitating the Genetic Counselling Process. Springer. doi:10.1007/978-3-319-74799-6. ISBN 978-3-319-74798-9. S2CID 13808432.

uct.ac.za

humangenetics.uct.ac.za

"Genetic Counselling Courses | Division of Human Genetics". humangenetics.uct.ac.za. Archived from the original on 2022-07-09. Retrieved 2018-08-15.

unimelb.edu.au

study.unimelb.edu.au

"Master of Genetic Counselling - The University of Melbourne". study.unimelb.edu.au. Retrieved 2024-02-21.

uptodate.com

Schattman GL, Xu K (17 November 2020). Wilkins-Haug L, Barss VA (eds.). "Preimplantation genetic testing". UpToDate.

uts.edu.au

"Course". University of Technology Sydney. Retrieved 2024-02-21.

web.archive.org

The American Cancer Society medical and editorial content team. "Family Cancer Syndromes". American Cancer Society. Archived from the original on 2013-08-02. Retrieved 2016-03-25.
"Genetic Counselling – Wits University". Johannesburg: The University of the Witwatersrand. Archived from the original on 2018-08-16. Retrieved 2018-08-15.
"Genetic Counselling Courses | Division of Human Genetics". humangenetics.uct.ac.za. Archived from the original on 2022-07-09. Retrieved 2018-08-15.
"Genetic Counselling South Africa". sashg.org. Archived from the original on 2018-08-16. Retrieved 2018-08-15.
"Overseas Applicants". Genetic Counsellor Registration Board. Archived from the original on 2021-04-29. Retrieved 2021-04-29.
"Home". www.asgc.org.au. Archived from the original on 2024-07-21. Retrieved 2025-01-13.
"Accredited Programs". gceducation.org. Archived from the original on 2018-12-09. Retrieved 2018-10-01.
"States Issuing Licenses for Genetic Counselors". National Society of Genetic Counselors. Archived from the original on 16 July 2018. Retrieved 3 October 2018.
"NSGC Blog". National Society of Genetic Counselors. Archived from the original on 15 August 2019. Retrieved 15 August 2019.
"Blogs: Black History Month: Bearing the torch of equity as an African-American genetic counselor and scientist". nsgc.org. National Society of Genetic Counselors. Archived from the original on 2021-01-20. Retrieved 2021-02-12.

wiley.com

Uhlmann WR, Schuette JL, Yashar BM (2009). "A Guide to Genetic Counseling".

onlinelibrary.wiley.com

Isbister, Joanne; Sexton, Adrienne; Forrest, Laura E.; James, Paul; Dowty, James; Taylor, Jessica; Austin, Jehannine; Winship, Ingrid (April 2023). "Psychiatric genetic counseling: A survey of Australian genetic counselors' practice and attitudes". Journal of Genetic Counseling. 32 (2): 495–502. doi:10.1002/jgc4.1659. ISSN 1059-7700. PMID 36480151. S2CID 254478392.

wits.ac.za

"Genetic Counselling – Wits University". Johannesburg: The University of the Witwatersrand. Archived from the original on 2018-08-16. Retrieved 2018-08-15.

worldcat.org

search.worldcat.org

Goldberg-Strassler D, Cabey R, Armenti EM, Jordan A (September 2016). "Preimplantation genetic diagnosis (PGD) genetic counseling; but why? The patient experience". Fertility and Sterility. 106 (3 Supplement): e370. doi:10.1016/j.fertnstert.2016.07.1053. ISSN 0015-0282.
Muthuswamy, Vasantha (October 2011). "Ethical issues in genetic counselling with special reference to haemoglobinopathies". The Indian Journal of Medical Research. 134 (4): 547–551. ISSN 0971-5916. PMC 3237255. PMID 22089619.
Isbister, Joanne; Sexton, Adrienne; Forrest, Laura E.; James, Paul; Dowty, James; Taylor, Jessica; Austin, Jehannine; Winship, Ingrid (April 2023). "Psychiatric genetic counseling: A survey of Australian genetic counselors' practice and attitudes". Journal of Genetic Counseling. 32 (2): 495–502. doi:10.1002/jgc4.1659. ISSN 1059-7700. PMID 36480151. S2CID 254478392.
Kanga-Parabia, Anaita; Mitchell, Lucas; Smyth, Renee; Kapoor, Trisha; Duggal, Jaitika; Pearn, Amy; Williams, Rachel; Courtney, Eliza; Edwards, Emma; Bowman, Michelle; Belekar, Mithila; Nisselle, Amy; Pearn, Amy; Kanga-Parabia, Anaita; Lundie, Ben (2024-05-07). "Genetic counseling workforce diversity, inclusion, and capacity in Australia and New Zealand". Genetics in Medicine Open: 101848. doi:10.1016/j.gimo.2024.101848. ISSN 2949-7744. PMC 11658314.
Yanes, Tatiane; Sullivan, Anna; Barbaro, Pasquale; Brion, Kristian; Hollway, Georgina; Peake, Jane; McNaughton, Peter (2023-10-01). "Evaluation and pilot testing of a multidisciplinary model of care to mainstream genomic testing for paediatric inborn errors of immunity". European Journal of Human Genetics. 31 (10): 1125–1132. doi:10.1038/s41431-023-01321-z. ISSN 1476-5438. PMC 10545723. PMID 36864115.
Bokkers, Kyra; Vlaming, Michiel; Engelhardt, Ellen G.; Zweemer, Ronald P.; van Oort, Inge M.; Kiemeney, Lambertus A. L. M.; Bleiker, Eveline M. A.; Ausems, Margreet G. E. M. (January 2022). "The Feasibility of Implementing Mainstream Germline Genetic Testing in Routine Cancer Care—A Systematic Review". Cancers. 14 (4): 1059. doi:10.3390/cancers14041059. ISSN 2072-6694. PMC 8870548. PMID 35205807.