Lissencephaly (English Wikipedia)

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

refsWebsite

Global rank English rank

26nih.gov

4^th place

17doi.org

2^nd place

6semanticscholar.org

11^th place

8^th place

1rarediseases.org

5,181^st place

3,260^th place

1orpha.net

3,537^th place

7,177^th place

1web.archive.org

1^st place

1specialchild.com

low place

doi.org

Fong KW, Ghai S, Toi A, Blaser S, Winsor EJ, Chitayat D (December 2004). "Prenatal ultrasound findings of lissencephaly associated with Miller-Dieker syndrome and comparison with pre- and postnatal magnetic resonance imaging". Ultrasound in Obstetrics & Gynecology. 24 (7): 716–23. doi:10.1002/uog.1777. PMID 15586369. S2CID 41862127.
Joseph LD, Kuruvilla S (2008). "Cytomegalovirus infection with lissencephaly". Indian Journal of Pathology & Microbiology. 51 (3): 402–4. doi:10.4103/0377-4929.42534. PMID 18723971.
Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA (September 2000). "Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations". Nature Genetics. 26 (1): 93–6. doi:10.1038/79246. PMID 10973257. S2CID 67748801.
Fernández V, Llinares-Benadero C, Borrell V (May 2016). "Cerebral cortex expansion and folding: what have we learned?". The EMBO Journal. 35 (10): 1021–44. doi:10.15252/embj.201593701. PMC 4868950. PMID 27056680.
Setty Y, Chen CC, Secrier M, Skoblov N, Kalamatianos D, Emmott S (September 2011). "How neurons migrate: a dynamic in-silico model of neuronal migration in the developing cortex". BMC Systems Biology. 5: 154. doi:10.1186/1752-0509-5-154. PMC 3198702. PMID 21962057.
Mochida GH (September 2009). "Genetics and biology of microcephaly and lissencephaly". Seminars in Pediatric Neurology. 16 (3): 120–6. doi:10.1016/j.spen.2009.07.001. PMC 3565221. PMID 19778709.
Kato M, Dobyns WB (April 2003). "Lissencephaly and the molecular basis of neuronal migration". Human Molecular Genetics. 12 (1): R89 – R96. doi:10.1093/hmg/ddg086. PMID 12668601.
Joseph LD, Pushpalatha, Kuruvilla S (2008). "Cytomegalovirus infection with lissencephaly". Indian Journal of Pathology & Microbiology. 51 (3): 402–404. doi:10.4103/0377-4929.42534. PMID 18723971.
Cardoso C, Leventer RJ, Ward HL, Toyo-Oka K, Chung J, Gross A, Martin CL, Allanson J, Pilz DT, Olney AH, Mutchinick OM, Hirotsune S, Wynshaw-Boris A, Dobyns WB, Ledbetter DH (April 2003). "Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3". American Journal of Human Genetics. 72 (4): 918–30. doi:10.1086/374320. PMC 1180354. PMID 12621583.
Shi CH, Zhang S, Yang ZH, Li YS, Liu YT, Li Z, Hu ZW, Xu YM (August 2018). "Identification of a novel PAFAH1B1 missense mutation as a cause of mild lissencephaly with basal ganglia calcification". Brain & Development. 41 (1): 29–35. doi:10.1016/j.braindev.2018.07.009. PMID 30100227. S2CID 51967262.
Deuel TA, Liu JS, Corbo JC, Yoo SY, Rorke-Adams LB, Walsh CA (January 2006). "Genetic interactions between doublecortin and doublecortin-like kinase in neuronal migration and axon outgrowth". Neuron. 49 (1): 41–53. doi:10.1016/j.neuron.2005.10.038. PMID 16387638. S2CID 15362872.
Nishikawa S, Goto S, Yamada K, Hamasaki T, Ushio Y (June 2003). "Lack of Reelin causes malpositioning of nigral dopaminergic neurons: evidence from comparison of normal and Reln(rl) mutant mice". The Journal of Comparative Neurology. 461 (2): 166–73. doi:10.1002/cne.10610. PMID 12724835. S2CID 9944380.
Aslan H, Gungorduk K, Yildirim D, Aslan O, Yildirim G, Ceylan Y (May 2009). "Prenatal diagnosis of lissencephaly: a case report". Journal of Clinical Ultrasound. 37 (4): 245–8. doi:10.1002/jcu.20572. PMID 19260111. S2CID 27735448.
Ghai S, Fong KW, Toi A, Chitayat D, Pantazi S, Blaser S (2006). "Prenatal US and MR imaging findings of lissencephaly: review of fetal cerebral sulcal development". Radiographics. 26 (2): 389–405. doi:10.1148/rg.262055059. PMID 16549605.
Forman MS, Squier W, Dobyns WB, Golden JA (October 2005). "Genotypically defined lissencephalies show distinct pathologies". Journal of Neuropathology and Experimental Neurology. 64 (10): 847–57. doi:10.1097/01.jnen.0000182978.56612.41. PMID 16215456.
Chong SS, Pack SD, Roschke AV, Tanigami A, Carrozzo R, Smith AC, Dobyns WB, Ledbetter DH (February 1997). "A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3". Human Molecular Genetics. 6 (2): 147–55. doi:10.1093/hmg/6.2.147. PMID 9063734.
Norman MG, Roberts M, Sirois J, Tremblay LJ (February 1976). "Lissencephaly". The Canadian Journal of Neurological Sciences. 3 (1): 39–46. doi:10.1017/S0317167100025981. PMID 175907.

nih.gov

pubmed.ncbi.nlm.nih.gov

Dobyns WB (1987). "Developmental aspects of lissencephaly and the lissencephaly syndromes". Birth Defects Original Article Series. 23 (1): 225–41. PMID 3472611.
Fong KW, Ghai S, Toi A, Blaser S, Winsor EJ, Chitayat D (December 2004). "Prenatal ultrasound findings of lissencephaly associated with Miller-Dieker syndrome and comparison with pre- and postnatal magnetic resonance imaging". Ultrasound in Obstetrics & Gynecology. 24 (7): 716–23. doi:10.1002/uog.1777. PMID 15586369. S2CID 41862127.
Joseph LD, Kuruvilla S (2008). "Cytomegalovirus infection with lissencephaly". Indian Journal of Pathology & Microbiology. 51 (3): 402–4. doi:10.4103/0377-4929.42534. PMID 18723971.
Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA (September 2000). "Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations". Nature Genetics. 26 (1): 93–6. doi:10.1038/79246. PMID 10973257. S2CID 67748801.
Fernández V, Llinares-Benadero C, Borrell V (May 2016). "Cerebral cortex expansion and folding: what have we learned?". The EMBO Journal. 35 (10): 1021–44. doi:10.15252/embj.201593701. PMC 4868950. PMID 27056680.
Setty Y, Chen CC, Secrier M, Skoblov N, Kalamatianos D, Emmott S (September 2011). "How neurons migrate: a dynamic in-silico model of neuronal migration in the developing cortex". BMC Systems Biology. 5: 154. doi:10.1186/1752-0509-5-154. PMC 3198702. PMID 21962057.
Mochida GH (September 2009). "Genetics and biology of microcephaly and lissencephaly". Seminars in Pediatric Neurology. 16 (3): 120–6. doi:10.1016/j.spen.2009.07.001. PMC 3565221. PMID 19778709.
Liu, J. S.; Schubert, C. R.; Walsh, C. A. (2012). "Rare genetic causes of lissencephaly may implicate microtubule-based transport in the pathogenesis of cortical dysplasias". In Noebels, J. L.; Avoli, M.; Rogawski, M. A.; Olsen, R. W.; Delgado-Escueta, A. V. (eds.). Jasper's Basic Mechanisms of the Epilepsies (4th ed.). Bethesda: National Center for Biotechnology Information. PMID 22787614.
Kato M, Dobyns WB (April 2003). "Lissencephaly and the molecular basis of neuronal migration". Human Molecular Genetics. 12 (1): R89 – R96. doi:10.1093/hmg/ddg086. PMID 12668601.
Joseph LD, Pushpalatha, Kuruvilla S (2008). "Cytomegalovirus infection with lissencephaly". Indian Journal of Pathology & Microbiology. 51 (3): 402–404. doi:10.4103/0377-4929.42534. PMID 18723971.
Cardoso C, Leventer RJ, Ward HL, Toyo-Oka K, Chung J, Gross A, Martin CL, Allanson J, Pilz DT, Olney AH, Mutchinick OM, Hirotsune S, Wynshaw-Boris A, Dobyns WB, Ledbetter DH (April 2003). "Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3". American Journal of Human Genetics. 72 (4): 918–30. doi:10.1086/374320. PMC 1180354. PMID 12621583.
Shi CH, Zhang S, Yang ZH, Li YS, Liu YT, Li Z, Hu ZW, Xu YM (August 2018). "Identification of a novel PAFAH1B1 missense mutation as a cause of mild lissencephaly with basal ganglia calcification". Brain & Development. 41 (1): 29–35. doi:10.1016/j.braindev.2018.07.009. PMID 30100227. S2CID 51967262.
Deuel TA, Liu JS, Corbo JC, Yoo SY, Rorke-Adams LB, Walsh CA (January 2006). "Genetic interactions between doublecortin and doublecortin-like kinase in neuronal migration and axon outgrowth". Neuron. 49 (1): 41–53. doi:10.1016/j.neuron.2005.10.038. PMID 16387638. S2CID 15362872.
Nishikawa S, Goto S, Yamada K, Hamasaki T, Ushio Y (June 2003). "Lack of Reelin causes malpositioning of nigral dopaminergic neurons: evidence from comparison of normal and Reln(rl) mutant mice". The Journal of Comparative Neurology. 461 (2): 166–73. doi:10.1002/cne.10610. PMID 12724835. S2CID 9944380.
Aslan H, Gungorduk K, Yildirim D, Aslan O, Yildirim G, Ceylan Y (May 2009). "Prenatal diagnosis of lissencephaly: a case report". Journal of Clinical Ultrasound. 37 (4): 245–8. doi:10.1002/jcu.20572. PMID 19260111. S2CID 27735448.
Cordes M, Cordes I, Sander B, Sperner J, Hedde JP (May 1988). "Lissencephaly: diagnosis by computed tomography and magnetic resonance imaging". European Journal of Radiology. 8 (2): 131–3. PMID 3383858.
Ghai S, Fong KW, Toi A, Chitayat D, Pantazi S, Blaser S (2006). "Prenatal US and MR imaging findings of lissencephaly: review of fetal cerebral sulcal development". Radiographics. 26 (2): 389–405. doi:10.1148/rg.262055059. PMID 16549605.
Dorovini-Zis K, Dolman CL (April 1977). "Gestational development of brain". Archives of Pathology & Laboratory Medicine. 101 (4): 192–5. PMID 576786.
Forman MS, Squier W, Dobyns WB, Golden JA (October 2005). "Genotypically defined lissencephalies show distinct pathologies". Journal of Neuropathology and Experimental Neurology. 64 (10): 847–57. doi:10.1097/01.jnen.0000182978.56612.41. PMID 16215456.
Chong SS, Pack SD, Roschke AV, Tanigami A, Carrozzo R, Smith AC, Dobyns WB, Ledbetter DH (February 1997). "A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3". Human Molecular Genetics. 6 (2): 147–55. doi:10.1093/hmg/6.2.147. PMID 9063734.
Norman MG, Roberts M, Sirois J, Tremblay LJ (February 1976). "Lissencephaly". The Canadian Journal of Neurological Sciences. 3 (1): 39–46. doi:10.1017/S0317167100025981. PMID 175907.

ncbi.nlm.nih.gov

Fernández V, Llinares-Benadero C, Borrell V (May 2016). "Cerebral cortex expansion and folding: what have we learned?". The EMBO Journal. 35 (10): 1021–44. doi:10.15252/embj.201593701. PMC 4868950. PMID 27056680.
Setty Y, Chen CC, Secrier M, Skoblov N, Kalamatianos D, Emmott S (September 2011). "How neurons migrate: a dynamic in-silico model of neuronal migration in the developing cortex". BMC Systems Biology. 5: 154. doi:10.1186/1752-0509-5-154. PMC 3198702. PMID 21962057.
Mochida GH (September 2009). "Genetics and biology of microcephaly and lissencephaly". Seminars in Pediatric Neurology. 16 (3): 120–6. doi:10.1016/j.spen.2009.07.001. PMC 3565221. PMID 19778709.
Cardoso C, Leventer RJ, Ward HL, Toyo-Oka K, Chung J, Gross A, Martin CL, Allanson J, Pilz DT, Olney AH, Mutchinick OM, Hirotsune S, Wynshaw-Boris A, Dobyns WB, Ledbetter DH (April 2003). "Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3". American Journal of Human Genetics. 72 (4): 918–30. doi:10.1086/374320. PMC 1180354. PMID 12621583.

ninds.nih.gov

"Lissencephaly Information Page". National Institute of Neurological Disorders and Stroke. Retrieved 2019-10-31.

orpha.net

Microlissencephaly

rarediseases.org

"Lissencephaly". National Organisation for Rare Diseases (NORD). NORD Rare Disease Database. 2018. Retrieved 20 May 2018.

semanticscholar.org

api.semanticscholar.org

Fong KW, Ghai S, Toi A, Blaser S, Winsor EJ, Chitayat D (December 2004). "Prenatal ultrasound findings of lissencephaly associated with Miller-Dieker syndrome and comparison with pre- and postnatal magnetic resonance imaging". Ultrasound in Obstetrics & Gynecology. 24 (7): 716–23. doi:10.1002/uog.1777. PMID 15586369. S2CID 41862127.
Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA (September 2000). "Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations". Nature Genetics. 26 (1): 93–6. doi:10.1038/79246. PMID 10973257. S2CID 67748801.
Shi CH, Zhang S, Yang ZH, Li YS, Liu YT, Li Z, Hu ZW, Xu YM (August 2018). "Identification of a novel PAFAH1B1 missense mutation as a cause of mild lissencephaly with basal ganglia calcification". Brain & Development. 41 (1): 29–35. doi:10.1016/j.braindev.2018.07.009. PMID 30100227. S2CID 51967262.
Deuel TA, Liu JS, Corbo JC, Yoo SY, Rorke-Adams LB, Walsh CA (January 2006). "Genetic interactions between doublecortin and doublecortin-like kinase in neuronal migration and axon outgrowth". Neuron. 49 (1): 41–53. doi:10.1016/j.neuron.2005.10.038. PMID 16387638. S2CID 15362872.
Nishikawa S, Goto S, Yamada K, Hamasaki T, Ushio Y (June 2003). "Lack of Reelin causes malpositioning of nigral dopaminergic neurons: evidence from comparison of normal and Reln(rl) mutant mice". The Journal of Comparative Neurology. 461 (2): 166–73. doi:10.1002/cne.10610. PMID 12724835. S2CID 9944380.
Aslan H, Gungorduk K, Yildirim D, Aslan O, Yildirim G, Ceylan Y (May 2009). "Prenatal diagnosis of lissencephaly: a case report". Journal of Clinical Ultrasound. 37 (4): 245–8. doi:10.1002/jcu.20572. PMID 19260111. S2CID 27735448.

specialchild.com

Baker, Lisa. "Lissencephaly". The Resource Foundation for Children with Challenges. Archived from the original on 2 June 2013. Retrieved 10 May 2013.

web.archive.org

Baker, Lisa. "Lissencephaly". The Resource Foundation for Children with Challenges. Archived from the original on 2 June 2013. Retrieved 10 May 2013.