Microcephaly (English Wikipedia)

Faheem, Muhammad; Naseer, Muhammad Imran; Rasool, Mahmood; Chaudhary, Adeel G; Kumosani, Taha A; Ilyas, Asad Muhammad; Pushparaj, Peter Natesan; Ahmed, Farid; Algahtani, Hussain A; Al-Qahtani, Mohammad H; Saleh Jamal, Hasan (2015-01-15). "Molecular genetics of human primary microcephaly: an overview". BMC Medical Genomics. 8 (Suppl 1): S4. doi:10.1186/1755-8794-8-S1-S4. ISSN 1755-8794. PMC 4315316. PMID 25951892.
Leviton, A.; Holmes, L.B.; Allred, E.N.; Vargas, J. (2002). "Methodologic issues in epidemiologic studies of congenital microcephaly". Early Hum Dev. 69 (1): 91–105. doi:10.1016/S0378-3782(02)00065-8. PMID 12324187.
Stoler-Poria, S.; Lev, D.; Schweiger, A.; Lerman-Sagie, T.; Malinger, G. (2010-01-12). "Developmental outcome of isolated fetal microcephaly". Ultrasound in Obstetrics and Gynecology. 36 (2). Wiley: 154–158. doi:10.1002/uog.7556. ISSN 0960-7692. PMID 20069548. S2CID 30379486.
Ashwal, S.; Michelson, D.; Plawner, L.; Dobyns, W. B. (2009). "Practice Parameter: Evaluation of the child with microcephaly (an evidence-based review)". Neurology. 73 (11): 887–897. doi:10.1212/WNL.0b013e3181b783f7. PMC 2744281. PMID 19752457.
Opladen T, López-Laso E, Cortès-Saladelafont E, Pearson TS, Sivri HS, Yildiz Y, Assmann B, Kurian MA, Leuzzi V, Heales S, Pope S, Porta F, García-Cazorla A, Honzík T, Pons R, Regal L, Goez H, Artuch R, Hoffmann GF, Horvath G, Thöny B, Scholl-Bürgi S, Burlina A, Verbeek MM, Mastrangelo M, Friedman J, Wassenberg T, Jeltsch K, Kulhánek J, Kuseyri Hübschmann O (May 2020). "Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies". Orphanet Journal of Rare Diseases. 15 (1): 126. doi:10.1186/s13023-020-01379-8. PMC 7251883. PMID 32456656.
Szczepanski, Sandra; Hussain, MuhammadSajid; Sur, Ilknur; Altmüller, Janine; Thiele, Holger; Abdullah, Uzma; Waseem, SyedaSeema; Moawia, Abubakar; Nürnberg, Gudrun; Noegel, Angelika Anna; Baig, Shahid Mahmood; Nürnberg, Peter (30 November 2015). "A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family". Human Genetics. 135 (2): 157–170. doi:10.1007/s00439-015-1619-5. PMID 26621532. S2CID 2295608.
Emily E. Petersen; Erin Staples; Dana Meaney-Delman; Marc Fischer; Sascha R. Ellington; William M. Callaghan; Denise J. Jamieson (January 22, 2016). "Interim Guidelines for Pregnant Women During a Zika Virus Outbreak — United States, 2016". Morbidity and Mortality Weekly Report. 65 (2): 30–33. doi:10.15585/mmwr.mm6502e1. PMID 26796813.
Reddy, Nihaal; Calloni, Sonia F.; Vernon, Hilary J.; Boltshauser, Eugen; Huisman, Thierry A. G. M.; Soares, Bruno P. (2018-05-01). "Neuroimaging Findings of Organic Acidemias and Aminoacidopathies". RadioGraphics. 38 (3): 912–931. doi:10.1148/rg.2018170042. ISSN 0271-5333. PMID 29757724.
Donald, Kirsten A.; Walker, Kathleen G.; Kilborn, Tracy; Carrara, Henri; Langerak, Nelleke G; Eley, Brian; Wilmshurst, Jo M (2015). "HIV Encephalopathy: pediatric case series description and insights from the clinic coalface". AIDS Research and Therapy. 12 (1): 2. doi:10.1186/s12981-014-0042-7. ISSN 1742-6405. PMC 4297380. PMID 25598835.
Tibussek, Daniel; Sinclair, Adriane; Yau, Ivanna; Teatero, Sarah; Fittipaldi, Nahuel; Richardson, Susan E.; Mayatepek, Ertan; Jahn, Peter; Askalan, Rand (2015). "Late-Onset Group B Streptococcal Meningitis Has Cerebrovascular Complications". The Journal of Pediatrics. 166 (5): 1187–1192.e1. doi:10.1016/j.jpeds.2015.02.014. PMID 25919727.
Ramos, Regina; Viana, Rafaela; Brainer-Lima, Alessandra; Florêncio, Telma; Carvalho, Maria Durce; van Der Linden, Vanessa; Amorim, Antonio; Rocha, Maria Ângela; Medeiros, Fabíola (2017). "Perinatal Chikungunya Virus-Associated Encephalitis Leading to Postnatal-Onset Microcephaly and Optic Atrophy". The Pediatric Infectious Disease Journal. 37 (1): 94–95. doi:10.1097/INF.0000000000001690. ISSN 0891-3668. PMID 28737626. S2CID 31790738.
Kurian, Manju A; Jungbluth, Heinz (July 2014). "Genetic disorders of thyroid metabolism and brain development". Developmental Medicine and Child Neurology. 56 (7): 627–634. doi:10.1111/dmcn.12445. ISSN 0012-1622. PMC 4231219. PMID 24665922.
Damlich, Jennifer; Qato, Roa; Cruz, Meredith; Colon, Maria; Wilkins, Isabelle (2009-07-01). "Discussion: 'Microcephaly associated with congenital heart defect' by Barbu et al". American Journal of Obstetrics & Gynecology. 201 (1): e7–e12. doi:10.1016/j.ajog.2009.05.042. ISSN 0002-9378. PMID 19576365.
Crespi, B.; Stead, P.; Elliot, M. (January 2010). "Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 107 (Suppl 1): 1736–1741. Bibcode:2010PNAS..107.1736C. doi:10.1073/pnas.0906080106. PMC 2868282. PMID 19955444.
Stone, Jennifer L.; O'Donovan, Michael C.; Gurling, Hugh; Kirov, George K.; Blackwood, Douglas H. R.; Corvin, Aiden; et al. (September 2008). "Rare chromosomal deletions and duplications increase risk of schizophrenia". Nature. 455 (7210): 237–241. Bibcode:2008Natur.455..237S. doi:10.1038/nature07239. PMC 3912847. PMID 18668038.
Dumas L, Sikela JM (2009). "DUF1220 domains, cognitive disease, and human brain evolution". Cold Spring Harb. Symp. Quant. Biol. 74: 375–382. doi:10.1101/sqb.2009.74.025. PMC 2902282. PMID 19850849.
Rimol, Lars M.; Agartz, Ingrid; Djurovic, Srdjan; Brown, Andrew A.; Roddey, J. Cooper; Kahler, Anna K.; et al. (2010). "Sex-dependent association of common variants of microcephaly genes with brain structure". Proceedings of the National Academy of Sciences. 107 (1): 384–388. Bibcode:2010PNAS..107..384R. doi:10.1073/pnas.0908454107. JSTOR 40536283. PMC 2806758. PMID 20080800.
Rasmussen, Sonja A.; Jamieson, Denise J.; Honein, Margaret A.; Petersen, Lyle R. (13 April 2016). "Zika Virus and Birth Defects — Reviewing the Evidence for Causality". New England Journal of Medicine. 374 (20): 1981–1987. doi:10.1056/NEJMsr1604338. PMID 27074377. S2CID 20675635.
Mlakar, Jernej; Korva, Misa; Tul, Nataša; Popović, Mara; Poljšak-Prijatelj, Mateja; Mraz, Jerica; Kolenc, Marko; Resman Rus, Katarina; Vesnaver Vipotnik, Tina (2016-03-10). "Zika Virus Associated with Microcephaly". New England Journal of Medicine. 374 (10): 951–958. doi:10.1056/NEJMoa1600651. ISSN 0028-4793. PMID 26862926. S2CID 205099844.
Cavallin, Mara; Rujano, Maria A.; Bednarek, Nathalie; Medina-Cano, Daniel; Bernabe Gelot, Antoinette; Drunat, Severine; Maillard, Camille; Garfa-Traore, Meriem; Bole, Christine (2017-10-01). "WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells". Brain. 140 (10): 2597–2609. doi:10.1093/brain/awx218. ISSN 1460-2156. PMID 28969387.
Adams, Hieab H. H.; Hibar, Derrek P.; Chouraki, Vincent; Stein, Jason L.; Nyquist, Paul A.; Rentería, Miguel E.; Trompet, Stella; Arias-Vasquez, Alejandro; Seshadri, Sudha (2016). "Novel genetic loci underlying human intracranial volume identified through genome-wide association". Nature Neuroscience. 19 (12): 1569–1582. doi:10.1038/nn.4398. PMC 5227112. PMID 27694991.
Jamuar, SS; Walsh, CA (June 2015). "Genomic variants and variations in malformations of cortical development". Pediatric Clinics of North America. 62 (3): 571–85. doi:10.1016/j.pcl.2015.03.002. PMC 4449454. PMID 26022163.
Rash, BG; Lim, HD; Breunig, JJ; Vaccarino, FM (26 October 2011). "FGF signaling expands embryonic cortical surface area by regulating Notch-dependent neurogenesis". The Journal of Neuroscience. 31 (43): 15604–17. doi:10.1523/jneurosci.4439-11.2011. PMC 3235689. PMID 22031906.
Shen, J; Gilmore, EC; Marshall, CA; Haddadin, M; Reynolds, JJ; Eyaid, W; Bodell, A; Barry, B; Gleason, D; Allen, K; Ganesh, VS; Chang, BS; Grix, A; Hill, RS; Topcu, M; Caldecott, KW; Barkovich, AJ; Walsh, CA (March 2010). "Mutations in PNKP cause microcephaly, seizures and defects in DNA repair". Nature Genetics. 42 (3): 245–9. doi:10.1038/ng.526. PMC 2835984. PMID 20118933.
Alkuraya, FS; Cai, X; Emery, C; Mochida, GH; Al-Dosari, MS; Felie, JM; Hill, RS; Barry, BJ; Partlow, JN; Gascon, GG; Kentab, A; Jan, M; Shaheen, R; Feng, Y; Walsh, CA (13 May 2011). "Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]". American Journal of Human Genetics. 88 (5): 536–47. doi:10.1016/j.ajhg.2011.04.003. PMC 3146728. PMID 21529751.
Johnson, Matthew B.; Sun, Xingshen; Kodani, Andrew; Borges-Monroy, Rebeca; Girskis, Kelly M.; Ryu, Steven C.; Wang, Peter P.; Patel, Komal; Gonzalez, Dilenny M.; Woo, Yu Mi; Yan, Ziying; Liang, Bo; Smith, Richard S.; Chatterjee, Manavi; Coman, Daniel; Papademetris, Xenophon; Staib, Lawrence H.; Hyder, Fahmeed; Mandeville, Joseph B.; Grant, P. Ellen; Im, Kiho; Kwak, Hojoong; Engelhardt, John F.; Walsh, Christopher A.; Bae, Byoung-Il (2018). "Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size". Nature. 556 (7701): 370–375. Bibcode:2018Natur.556..370J. doi:10.1038/s41586-018-0035-0. ISSN 0028-0836. PMC 6095461. PMID 29643508.
Nowakowski, TJ; Pollen, AA; Di Lullo, E; Sandoval-Espinosa, C; Bershteyn, M; Kriegstein, AR (5 May 2016). "Expression Analysis Highlights AXL as a Candidate Zika Virus Entry Receptor in Neural Stem Cells". Cell Stem Cell. 18 (5): 591–6. doi:10.1016/j.stem.2016.03.012. PMC 4860115. PMID 27038591.
Li, C; Xu, D; Ye, Q; Hong, S; Jiang, Y; Liu, X; Zhang, N; Shi, L; Qin, CF; Xu, Z (7 July 2016). "Zika Virus Disrupts Neural Progenitor Development and Leads to Microcephaly in Mice". Cell Stem Cell. 19 (1): 120–6. doi:10.1016/j.stem.2016.04.017. PMID 27179424.
de Koning, T. J. (2006). "Treatment with amino acids in serine deficiency disorders". Journal of Inherited Metabolic Disease. 29 (2–3): 347–351. doi:10.1007/s10545-006-0269-0. ISSN 0141-8955. PMID 16763900. S2CID 35908740.
Mateen, F.J.; Boes, C.J. (2010). "'Pinheads': the exhibition of neurologic disorders at 'The Greatest Show on Earth'". Neurology. 75 (22): 2028–32. doi:10.1212/WNL.0b013e3181ff9636. PMID 21115959. S2CID 207118420.
Kozma, Chahira (10 October 2005). "Historical Review - Dwarfs in Ancient Egypt" (PDF). American Journal of Medical Genetics. 140 (4). Wiley-Liss, Inc: 303–311. doi:10.1002/ajmg.a.31068. PMID 16380966. S2CID 797288. Archived (PDF) from the original on 17 May 2017. Retrieved 17 February 2018.

harvard.edu

ui.adsabs.harvard.edu

Crespi, B.; Stead, P.; Elliot, M. (January 2010). "Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 107 (Suppl 1): 1736–1741. Bibcode:2010PNAS..107.1736C. doi:10.1073/pnas.0906080106. PMC 2868282. PMID 19955444.
Stone, Jennifer L.; O'Donovan, Michael C.; Gurling, Hugh; Kirov, George K.; Blackwood, Douglas H. R.; Corvin, Aiden; et al. (September 2008). "Rare chromosomal deletions and duplications increase risk of schizophrenia". Nature. 455 (7210): 237–241. Bibcode:2008Natur.455..237S. doi:10.1038/nature07239. PMC 3912847. PMID 18668038.
Rimol, Lars M.; Agartz, Ingrid; Djurovic, Srdjan; Brown, Andrew A.; Roddey, J. Cooper; Kahler, Anna K.; et al. (2010). "Sex-dependent association of common variants of microcephaly genes with brain structure". Proceedings of the National Academy of Sciences. 107 (1): 384–388. Bibcode:2010PNAS..107..384R. doi:10.1073/pnas.0908454107. JSTOR 40536283. PMC 2806758. PMID 20080800.
Johnson, Matthew B.; Sun, Xingshen; Kodani, Andrew; Borges-Monroy, Rebeca; Girskis, Kelly M.; Ryu, Steven C.; Wang, Peter P.; Patel, Komal; Gonzalez, Dilenny M.; Woo, Yu Mi; Yan, Ziying; Liang, Bo; Smith, Richard S.; Chatterjee, Manavi; Coman, Daniel; Papademetris, Xenophon; Staib, Lawrence H.; Hyder, Fahmeed; Mandeville, Joseph B.; Grant, P. Ellen; Im, Kiho; Kwak, Hojoong; Engelhardt, John F.; Walsh, Christopher A.; Bae, Byoung-Il (2018). "Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size". Nature. 556 (7701): 370–375. Bibcode:2018Natur.556..370J. doi:10.1038/s41586-018-0035-0. ISSN 0028-0836. PMC 6095461. PMID 29643508.

jstor.org

Rimol, Lars M.; Agartz, Ingrid; Djurovic, Srdjan; Brown, Andrew A.; Roddey, J. Cooper; Kahler, Anna K.; et al. (2010). "Sex-dependent association of common variants of microcephaly genes with brain structure". Proceedings of the National Academy of Sciences. 107 (1): 384–388. Bibcode:2010PNAS..107..384R. doi:10.1073/pnas.0908454107. JSTOR 40536283. PMC 2806758. PMID 20080800.

malacards.org

"Microcephaly with Spastic Quadriplegia disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials". www.malacards.org. Retrieved 2019-08-02.

mayoclinic.org

"Microcephaly - Symptoms and causes". Mayo Clinic. Retrieved 2019-07-30.

medlineplus.gov

"Trisomy 18: MedlinePlus Medical Encyclopedia". medlineplus.gov. Retrieved 2020-10-29.

merriam-webster.com

"Microcephaly - Definition of Microcephaly by Merriam-Webster". Archived from the original on 2014-09-14.

mito.org.au

"Mito Info". Mito Foundation. Retrieved 2019-08-01.

nih.gov

pubmed.ncbi.nlm.nih.gov

Faheem, Muhammad; Naseer, Muhammad Imran; Rasool, Mahmood; Chaudhary, Adeel G; Kumosani, Taha A; Ilyas, Asad Muhammad; Pushparaj, Peter Natesan; Ahmed, Farid; Algahtani, Hussain A; Al-Qahtani, Mohammad H; Saleh Jamal, Hasan (2015-01-15). "Molecular genetics of human primary microcephaly: an overview". BMC Medical Genomics. 8 (Suppl 1): S4. doi:10.1186/1755-8794-8-S1-S4. ISSN 1755-8794. PMC 4315316. PMID 25951892.
Leviton, A.; Holmes, L.B.; Allred, E.N.; Vargas, J. (2002). "Methodologic issues in epidemiologic studies of congenital microcephaly". Early Hum Dev. 69 (1): 91–105. doi:10.1016/S0378-3782(02)00065-8. PMID 12324187.
Opitz, J. M.; Holt, M. C. (1990). "Microcephaly: general considerations and aids to nosology". Journal of Craniofacial Genetics and Developmental Biology. 10 (2): 75–204. PMID 2211965.
Stoler-Poria, S.; Lev, D.; Schweiger, A.; Lerman-Sagie, T.; Malinger, G. (2010-01-12). "Developmental outcome of isolated fetal microcephaly". Ultrasound in Obstetrics and Gynecology. 36 (2). Wiley: 154–158. doi:10.1002/uog.7556. ISSN 0960-7692. PMID 20069548. S2CID 30379486.
Ashwal, S.; Michelson, D.; Plawner, L.; Dobyns, W. B. (2009). "Practice Parameter: Evaluation of the child with microcephaly (an evidence-based review)". Neurology. 73 (11): 887–897. doi:10.1212/WNL.0b013e3181b783f7. PMC 2744281. PMID 19752457.
Opladen T, López-Laso E, Cortès-Saladelafont E, Pearson TS, Sivri HS, Yildiz Y, Assmann B, Kurian MA, Leuzzi V, Heales S, Pope S, Porta F, García-Cazorla A, Honzík T, Pons R, Regal L, Goez H, Artuch R, Hoffmann GF, Horvath G, Thöny B, Scholl-Bürgi S, Burlina A, Verbeek MM, Mastrangelo M, Friedman J, Wassenberg T, Jeltsch K, Kulhánek J, Kuseyri Hübschmann O (May 2020). "Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies". Orphanet Journal of Rare Diseases. 15 (1): 126. doi:10.1186/s13023-020-01379-8. PMC 7251883. PMID 32456656.
Szczepanski, Sandra; Hussain, MuhammadSajid; Sur, Ilknur; Altmüller, Janine; Thiele, Holger; Abdullah, Uzma; Waseem, SyedaSeema; Moawia, Abubakar; Nürnberg, Gudrun; Noegel, Angelika Anna; Baig, Shahid Mahmood; Nürnberg, Peter (30 November 2015). "A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family". Human Genetics. 135 (2): 157–170. doi:10.1007/s00439-015-1619-5. PMID 26621532. S2CID 2295608.
Emily E. Petersen; Erin Staples; Dana Meaney-Delman; Marc Fischer; Sascha R. Ellington; William M. Callaghan; Denise J. Jamieson (January 22, 2016). "Interim Guidelines for Pregnant Women During a Zika Virus Outbreak — United States, 2016". Morbidity and Mortality Weekly Report. 65 (2): 30–33. doi:10.15585/mmwr.mm6502e1. PMID 26796813.
Reddy, Nihaal; Calloni, Sonia F.; Vernon, Hilary J.; Boltshauser, Eugen; Huisman, Thierry A. G. M.; Soares, Bruno P. (2018-05-01). "Neuroimaging Findings of Organic Acidemias and Aminoacidopathies". RadioGraphics. 38 (3): 912–931. doi:10.1148/rg.2018170042. ISSN 0271-5333. PMID 29757724.
Joyce, Tina; Huecker, Martin R. (2019), "Pediatric Abusive Head Trauma (Shaken Baby Syndrome)", National Center for Biotechnology Information, AU.S. National Library of Medicine, PMID 29763011, retrieved 2019-07-30
Donald, Kirsten A.; Walker, Kathleen G.; Kilborn, Tracy; Carrara, Henri; Langerak, Nelleke G; Eley, Brian; Wilmshurst, Jo M (2015). "HIV Encephalopathy: pediatric case series description and insights from the clinic coalface". AIDS Research and Therapy. 12 (1): 2. doi:10.1186/s12981-014-0042-7. ISSN 1742-6405. PMC 4297380. PMID 25598835.
Tibussek, Daniel; Sinclair, Adriane; Yau, Ivanna; Teatero, Sarah; Fittipaldi, Nahuel; Richardson, Susan E.; Mayatepek, Ertan; Jahn, Peter; Askalan, Rand (2015). "Late-Onset Group B Streptococcal Meningitis Has Cerebrovascular Complications". The Journal of Pediatrics. 166 (5): 1187–1192.e1. doi:10.1016/j.jpeds.2015.02.014. PMID 25919727.
Ramos, Regina; Viana, Rafaela; Brainer-Lima, Alessandra; Florêncio, Telma; Carvalho, Maria Durce; van Der Linden, Vanessa; Amorim, Antonio; Rocha, Maria Ângela; Medeiros, Fabíola (2017). "Perinatal Chikungunya Virus-Associated Encephalitis Leading to Postnatal-Onset Microcephaly and Optic Atrophy". The Pediatric Infectious Disease Journal. 37 (1): 94–95. doi:10.1097/INF.0000000000001690. ISSN 0891-3668. PMID 28737626. S2CID 31790738.
Kurian, Manju A; Jungbluth, Heinz (July 2014). "Genetic disorders of thyroid metabolism and brain development". Developmental Medicine and Child Neurology. 56 (7): 627–634. doi:10.1111/dmcn.12445. ISSN 0012-1622. PMC 4231219. PMID 24665922.
Damlich, Jennifer; Qato, Roa; Cruz, Meredith; Colon, Maria; Wilkins, Isabelle (2009-07-01). "Discussion: 'Microcephaly associated with congenital heart defect' by Barbu et al". American Journal of Obstetrics & Gynecology. 201 (1): e7–e12. doi:10.1016/j.ajog.2009.05.042. ISSN 0002-9378. PMID 19576365.
Crespi, B.; Stead, P.; Elliot, M. (January 2010). "Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 107 (Suppl 1): 1736–1741. Bibcode:2010PNAS..107.1736C. doi:10.1073/pnas.0906080106. PMC 2868282. PMID 19955444.
Stone, Jennifer L.; O'Donovan, Michael C.; Gurling, Hugh; Kirov, George K.; Blackwood, Douglas H. R.; Corvin, Aiden; et al. (September 2008). "Rare chromosomal deletions and duplications increase risk of schizophrenia". Nature. 455 (7210): 237–241. Bibcode:2008Natur.455..237S. doi:10.1038/nature07239. PMC 3912847. PMID 18668038.
Dumas L, Sikela JM (2009). "DUF1220 domains, cognitive disease, and human brain evolution". Cold Spring Harb. Symp. Quant. Biol. 74: 375–382. doi:10.1101/sqb.2009.74.025. PMC 2902282. PMID 19850849.
Rimol, Lars M.; Agartz, Ingrid; Djurovic, Srdjan; Brown, Andrew A.; Roddey, J. Cooper; Kahler, Anna K.; et al. (2010). "Sex-dependent association of common variants of microcephaly genes with brain structure". Proceedings of the National Academy of Sciences. 107 (1): 384–388. Bibcode:2010PNAS..107..384R. doi:10.1073/pnas.0908454107. JSTOR 40536283. PMC 2806758. PMID 20080800.
Rasmussen, Sonja A.; Jamieson, Denise J.; Honein, Margaret A.; Petersen, Lyle R. (13 April 2016). "Zika Virus and Birth Defects — Reviewing the Evidence for Causality". New England Journal of Medicine. 374 (20): 1981–1987. doi:10.1056/NEJMsr1604338. PMID 27074377. S2CID 20675635.
Mlakar, Jernej; Korva, Misa; Tul, Nataša; Popović, Mara; Poljšak-Prijatelj, Mateja; Mraz, Jerica; Kolenc, Marko; Resman Rus, Katarina; Vesnaver Vipotnik, Tina (2016-03-10). "Zika Virus Associated with Microcephaly". New England Journal of Medicine. 374 (10): 951–958. doi:10.1056/NEJMoa1600651. ISSN 0028-4793. PMID 26862926. S2CID 205099844.
Cavallin, Mara; Rujano, Maria A.; Bednarek, Nathalie; Medina-Cano, Daniel; Bernabe Gelot, Antoinette; Drunat, Severine; Maillard, Camille; Garfa-Traore, Meriem; Bole, Christine (2017-10-01). "WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells". Brain. 140 (10): 2597–2609. doi:10.1093/brain/awx218. ISSN 1460-2156. PMID 28969387.
Burrow, Gerard N.; Hamilton, Howard B.; Hrubec, Zdenek (June 1964). "Study of Adolescents Exposed in Utero to the Atomic Bomb, Nagasaki, Japan". Yale Journal of Biology and Medicine. 36 (6): 430–444. ISSN 0044-0086. PMC 2604646. PMID 14173443.
Adams, Hieab H. H.; Hibar, Derrek P.; Chouraki, Vincent; Stein, Jason L.; Nyquist, Paul A.; Rentería, Miguel E.; Trompet, Stella; Arias-Vasquez, Alejandro; Seshadri, Sudha (2016). "Novel genetic loci underlying human intracranial volume identified through genome-wide association". Nature Neuroscience. 19 (12): 1569–1582. doi:10.1038/nn.4398. PMC 5227112. PMID 27694991.
Jamuar, SS; Walsh, CA (June 2015). "Genomic variants and variations in malformations of cortical development". Pediatric Clinics of North America. 62 (3): 571–85. doi:10.1016/j.pcl.2015.03.002. PMC 4449454. PMID 26022163.
Rash, BG; Lim, HD; Breunig, JJ; Vaccarino, FM (26 October 2011). "FGF signaling expands embryonic cortical surface area by regulating Notch-dependent neurogenesis". The Journal of Neuroscience. 31 (43): 15604–17. doi:10.1523/jneurosci.4439-11.2011. PMC 3235689. PMID 22031906.
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