Alagille syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Alagille syndrome" in English language version.

refsWebsite

Global rank English rank

28nih.gov

4^th place

16doi.org

2^nd place

3semanticscholar.org

11^th place

8^th place

3worldcat.org

5^th place

2fda.gov

447^th place

338^th place

1whonamedit.com

2,888^th place

2,730^th place

1zenodo.org

621^st place

380^th place

1childrenshospital.org

low place

1ucsf.edu

5,479^th place

3,911^th place

1lahey.org

low place

childrenshospital.org

"Alagille Syndrome - Diagnosis & Treatment". Boston Children's Hospital.

doi.org

Mitchell E, Gilbert M, Loomes KM (November 2018). "Alagille Syndrome". Clinics in Liver Disease. 22 (4): 625–641. doi:10.1016/j.cld.2018.06.001. PMID 30266153.
Ayoub MD, Kamath BM (August 2022). "Alagille Syndrome: Current Understanding of Pathogenesis, and Challenges in Diagnosis and Management". Clinics in Liver Disease. 26 (3): 355–370. doi:10.1016/j.cld.2022.03.002. PMID 35868679.
Alagille D, Odièvre M, Gautier M, Dommergues JP (January 1975). "Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur". The Journal of Pediatrics. 86 (1): 63–71. doi:10.1016/S0022-3476(75)80706-2. PMID 803282.
Ayoub MD, Bakhsh AA, Vandriel SM, Keitel V, Kamath BM (October 2023). "Management of adults with Alagille syndrome". Hepatology International. 17 (5): 1098–1112. doi:10.1007/s12072-023-10578-x. PMC 10522532. PMID 37584849.
Kamath BM, Baker A, Houwen R, Todorova L, Kerkar N (August 2018). "Systematic Review: The Epidemiology, Natural History, and Burden of Alagille Syndrome". Journal of Pediatric Gastroenterology and Nutrition. 67 (2). J Pediatr Gastroenterol Nutr: 148–156. doi:10.1097/MPG.0000000000001958. PMC 6110620. PMID 29543694.
Krantz ID, Piccoli DA, Spinner NB (February 1997). "Alagille syndrome". Journal of Medical Genetics. 34 (2): 152–157. doi:10.1136/jmg.34.2.152. PMC 1050871. PMID 9039994.
Sijmons RH (February 2008). "Encyclopaedia of tumour-associated familial disorders. Part I: from AIMAH to CHIME syndrome". Hereditary Cancer in Clinical Practice. 6 (1): 22–57. doi:10.1186/1897-4287-6-1-22. PMC 2735164. PMID 19706204.
Sokol RJ, Heubi JE, Balistreri WF (August 1983). "Intrahepatic "cholestasis facies": is it specific for Alagille syndrome?". The Journal of Pediatrics. 103 (2): 205–208. doi:10.1016/s0022-3476(83)80345-x. PMID 6875709.
Bissonnette ML, Lane JC, Chang A (May 2017). "Extreme Renal Pathology in Alagille Syndrome". Kidney International Reports. 2 (3): 493–497. doi:10.1016/j.ekir.2016.11.002. PMC 5720621. PMID 29318215.
Oda T, Elkahloun AG, Pike BL, Okajima K, Krantz ID, Genin A, et al. (July 1997). "Mutations in the human Jagged1 gene are responsible for Alagille syndrome". Nature Genetics. 16 (3): 235–242. doi:10.1038/ng0797-235. PMID 9207787. S2CID 5775213.
Kamath BM, Bauer RC, Loomes KM, Chao G, Gerfen J, Hutchinson A, et al. (February 2012). "NOTCH2 mutations in Alagille syndrome". Journal of Medical Genetics. 49 (2): 138–144. doi:10.1136/jmedgenet-2011-100544. PMC 3682659. PMID 22209762.
Vajro P, Ferrante L, Paolella G (June 2012). "Alagille syndrome: an overview". Clinics and Research in Hepatology and Gastroenterology. 36 (3): 275–277. doi:10.1016/j.clinre.2012.03.019. PMID 22521120.
Mitchell E, Gilbert M, Loomes KM (November 2018). "Alagille Syndrome". Clinics in Liver Disease. 22 (4). Springer: 625–641. doi:10.1016/j.cld.2018.06.001. PMID 30266153. S2CID 52883591.
Ohashi K, Togawa T, Sugiura T, Ito K, Endo T, Aoyama K, et al. (November 2017). "Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome". Acta Paediatrica. 106 (11): 1817–1824. doi:10.1111/apa.13981. PMID 28695677. S2CID 24604635.
Jesina D (2017-11-01). "Alagille Syndrome: An Overview". Neonatal Network. 36 (6): 343–347. doi:10.1891/0730-0832.36.6.343. ISSN 1539-2880. PMID 29185945.
Turnpenny PD, Ellard S (March 2012). "Alagille syndrome: pathogenesis, diagnosis and management". European Journal of Human Genetics. 20 (3): 251–257. doi:10.1038/ejhg.2011.181. ISSN 1476-5438. PMC 3283172. PMID 21934706.

fda.gov

accessdata.fda.gov

"Highlights of prescribing information: LIVMARLITM (maralixibat) oral solution" (PDF). Mirum Pharmaceuticals, Inc. U.S. Food and Drug Administration.
"Maralixibat: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). Retrieved 29 September 2021.

lahey.org

"Donor Requirements & Evaluation - Live Liver Transplant". Lahey Hospital & Medical Center, Burlington & Peabody. Retrieved 2019-10-08.

nih.gov

pubmed.ncbi.nlm.nih.gov

Mitchell E, Gilbert M, Loomes KM (November 2018). "Alagille Syndrome". Clinics in Liver Disease. 22 (4): 625–641. doi:10.1016/j.cld.2018.06.001. PMID 30266153.
Ayoub MD, Kamath BM (August 2022). "Alagille Syndrome: Current Understanding of Pathogenesis, and Challenges in Diagnosis and Management". Clinics in Liver Disease. 26 (3): 355–370. doi:10.1016/j.cld.2022.03.002. PMID 35868679.
Alagille D, Odièvre M, Gautier M, Dommergues JP (January 1975). "Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur". The Journal of Pediatrics. 86 (1): 63–71. doi:10.1016/S0022-3476(75)80706-2. PMID 803282.
Ayoub MD, Bakhsh AA, Vandriel SM, Keitel V, Kamath BM (October 2023). "Management of adults with Alagille syndrome". Hepatology International. 17 (5): 1098–1112. doi:10.1007/s12072-023-10578-x. PMC 10522532. PMID 37584849.
Diaz-Frias J, Kondamudi NP (2019). "Alagille Syndrome". StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing. PMID 29939604.
Kamath BM, Baker A, Houwen R, Todorova L, Kerkar N (August 2018). "Systematic Review: The Epidemiology, Natural History, and Burden of Alagille Syndrome". Journal of Pediatric Gastroenterology and Nutrition. 67 (2). J Pediatr Gastroenterol Nutr: 148–156. doi:10.1097/MPG.0000000000001958. PMC 6110620. PMID 29543694.
Krantz ID, Piccoli DA, Spinner NB (February 1997). "Alagille syndrome". Journal of Medical Genetics. 34 (2): 152–157. doi:10.1136/jmg.34.2.152. PMC 1050871. PMID 9039994.
Sijmons RH (February 2008). "Encyclopaedia of tumour-associated familial disorders. Part I: from AIMAH to CHIME syndrome". Hereditary Cancer in Clinical Practice. 6 (1): 22–57. doi:10.1186/1897-4287-6-1-22. PMC 2735164. PMID 19706204.
Sokol RJ, Heubi JE, Balistreri WF (August 1983). "Intrahepatic "cholestasis facies": is it specific for Alagille syndrome?". The Journal of Pediatrics. 103 (2): 205–208. doi:10.1016/s0022-3476(83)80345-x. PMID 6875709.
Bissonnette ML, Lane JC, Chang A (May 2017). "Extreme Renal Pathology in Alagille Syndrome". Kidney International Reports. 2 (3): 493–497. doi:10.1016/j.ekir.2016.11.002. PMC 5720621. PMID 29318215.
Oda T, Elkahloun AG, Pike BL, Okajima K, Krantz ID, Genin A, et al. (July 1997). "Mutations in the human Jagged1 gene are responsible for Alagille syndrome". Nature Genetics. 16 (3): 235–242. doi:10.1038/ng0797-235. PMID 9207787. S2CID 5775213.
Kamath BM, Bauer RC, Loomes KM, Chao G, Gerfen J, Hutchinson A, et al. (February 2012). "NOTCH2 mutations in Alagille syndrome". Journal of Medical Genetics. 49 (2): 138–144. doi:10.1136/jmedgenet-2011-100544. PMC 3682659. PMID 22209762.
Vajro P, Ferrante L, Paolella G (June 2012). "Alagille syndrome: an overview". Clinics and Research in Hepatology and Gastroenterology. 36 (3): 275–277. doi:10.1016/j.clinre.2012.03.019. PMID 22521120.
Mitchell E, Gilbert M, Loomes KM (November 2018). "Alagille Syndrome". Clinics in Liver Disease. 22 (4). Springer: 625–641. doi:10.1016/j.cld.2018.06.001. PMID 30266153. S2CID 52883591.
Ohashi K, Togawa T, Sugiura T, Ito K, Endo T, Aoyama K, et al. (November 2017). "Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome". Acta Paediatrica. 106 (11): 1817–1824. doi:10.1111/apa.13981. PMID 28695677. S2CID 24604635.
Jesina D (2017-11-01). "Alagille Syndrome: An Overview". Neonatal Network. 36 (6): 343–347. doi:10.1891/0730-0832.36.6.343. ISSN 1539-2880. PMID 29185945.
Turnpenny PD, Ellard S (March 2012). "Alagille syndrome: pathogenesis, diagnosis and management". European Journal of Human Genetics. 20 (3): 251–257. doi:10.1038/ejhg.2011.181. ISSN 1476-5438. PMC 3283172. PMID 21934706.

ncbi.nlm.nih.gov

Ayoub MD, Bakhsh AA, Vandriel SM, Keitel V, Kamath BM (October 2023). "Management of adults with Alagille syndrome". Hepatology International. 17 (5): 1098–1112. doi:10.1007/s12072-023-10578-x. PMC 10522532. PMID 37584849.
Diaz-Frias J, Kondamudi NP (2019). "Alagille Syndrome". StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing. PMID 29939604.
Kamath BM, Baker A, Houwen R, Todorova L, Kerkar N (August 2018). "Systematic Review: The Epidemiology, Natural History, and Burden of Alagille Syndrome". Journal of Pediatric Gastroenterology and Nutrition. 67 (2). J Pediatr Gastroenterol Nutr: 148–156. doi:10.1097/MPG.0000000000001958. PMC 6110620. PMID 29543694.
Krantz ID, Piccoli DA, Spinner NB (February 1997). "Alagille syndrome". Journal of Medical Genetics. 34 (2): 152–157. doi:10.1136/jmg.34.2.152. PMC 1050871. PMID 9039994.
Sijmons RH (February 2008). "Encyclopaedia of tumour-associated familial disorders. Part I: from AIMAH to CHIME syndrome". Hereditary Cancer in Clinical Practice. 6 (1): 22–57. doi:10.1186/1897-4287-6-1-22. PMC 2735164. PMID 19706204.
Bissonnette ML, Lane JC, Chang A (May 2017). "Extreme Renal Pathology in Alagille Syndrome". Kidney International Reports. 2 (3): 493–497. doi:10.1016/j.ekir.2016.11.002. PMC 5720621. PMID 29318215.
Kamath BM, Bauer RC, Loomes KM, Chao G, Gerfen J, Hutchinson A, et al. (February 2012). "NOTCH2 mutations in Alagille syndrome". Journal of Medical Genetics. 49 (2): 138–144. doi:10.1136/jmedgenet-2011-100544. PMC 3682659. PMID 22209762.
Turnpenny PD, Ellard S (March 2012). "Alagille syndrome: pathogenesis, diagnosis and management". European Journal of Human Genetics. 20 (3): 251–257. doi:10.1038/ejhg.2011.181. ISSN 1476-5438. PMC 3283172. PMID 21934706.

ghr.nlm.nih.gov

"Alagille syndrome". Genetics Home Reference. U.S. National Library of Medicine. Retrieved 31 October 2016.
"What is a gene mutation and how do mutations occur?". Genetics Home Reference. U.S. National Library of Medicine.

niddk.nih.gov

"Symptoms & Causes for Alagille Syndrome". National Institute of Diabetes and Digestive and Kidney Diseases.

semanticscholar.org

api.semanticscholar.org

Oda T, Elkahloun AG, Pike BL, Okajima K, Krantz ID, Genin A, et al. (July 1997). "Mutations in the human Jagged1 gene are responsible for Alagille syndrome". Nature Genetics. 16 (3): 235–242. doi:10.1038/ng0797-235. PMID 9207787. S2CID 5775213.
Mitchell E, Gilbert M, Loomes KM (November 2018). "Alagille Syndrome". Clinics in Liver Disease. 22 (4). Springer: 625–641. doi:10.1016/j.cld.2018.06.001. PMID 30266153. S2CID 52883591.
Ohashi K, Togawa T, Sugiura T, Ito K, Endo T, Aoyama K, et al. (November 2017). "Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome". Acta Paediatrica. 106 (11): 1817–1824. doi:10.1111/apa.13981. PMID 28695677. S2CID 24604635.

ucsf.edu

surgery.ucsf.edu

"Alagille Syndrome". Department of Surgery. University of California - San Francisco. Retrieved 2019-10-08.

whonamedit.com

synd/729 at Who Named It?

worldcat.org

search.worldcat.org

Jesina D (2017-11-01). "Alagille Syndrome: An Overview". Neonatal Network. 36 (6): 343–347. doi:10.1891/0730-0832.36.6.343. ISSN 1539-2880. PMID 29185945.
Doria C (2016). Doria C (ed.). Contemporary Liver Transplantation : The Successful Liver Transplant Program. Springer. ISBN 9783319055435. OCLC 1111825084.
Turnpenny PD, Ellard S (March 2012). "Alagille syndrome: pathogenesis, diagnosis and management". European Journal of Human Genetics. 20 (3): 251–257. doi:10.1038/ejhg.2011.181. ISSN 1476-5438. PMC 3283172. PMID 21934706.

zenodo.org

Oda T, Elkahloun AG, Pike BL, Okajima K, Krantz ID, Genin A, et al. (July 1997). "Mutations in the human Jagged1 gene are responsible for Alagille syndrome". Nature Genetics. 16 (3): 235–242. doi:10.1038/ng0797-235. PMID 9207787. S2CID 5775213.