Polymicrogyria (English Wikipedia)

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

refsWebsite

Global rank English rank

30nih.gov

4^th place

14doi.org

2^nd place

3worldcat.org

5^th place

2semanticscholar.org

11^th place

8^th place

1orpha.net

3,537^th place

7,177^th place

doi.org

Leventer RJ, Jansen A, Pilz DT, Stoodley N, Marini C, Dubeau F, Malone J, Mitchell LA, Mandelstam S, Scheffer IE, Berkovic SF, Andermann F, Andermann E, Guerrini R, Dobyns WB (May 2010). "Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients". Brain: A Journal of Neurology. 133 (Pt 5): 1415–27. doi:10.1093/brain/awq078. PMC 2859156. PMID 20403963.
Jansen, A.; Andermann, E. (1 May 2005). "Genetics of the polymicrogyria syndromes". Journal of Medical Genetics. 42 (5): 369–378. doi:10.1136/jmg.2004.023952. PMC 1736054. PMID 15863665.
Smith, RS; Kenny, CJ; Ganesh, V; Jang, A; Borges-Monroy, R; Partlow, JN; Hill, RS; Shin, T; Chen, AY; Doan, RN; Anttonen, AK; Ignatius, J; Medne, L; Bönnemann, CG; Hecht, JL; Salonen, O; Barkovich, AJ; Poduri, A; Wilke, M; de Wit, MCY; Mancini, GMS; Sztriha, L; Im, K; Amrom, D; Andermann, E; Paetau, R; Lehesjoki, AE; Walsh, CA; Lehtinen, MK (5 September 2018). "Sodium Channel SCN3A (Na_V1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development". Neuron. 99 (5): 905–913.e7. doi:10.1016/j.neuron.2018.07.052. PMC 6226006. PMID 30146301.
Stutterd CA, Leventer RJ (June 2014). "Polymicrogyria: a common and heterogeneous malformation of cortical development". Am J Med Genet C Semin Med Genet. 166C (2): 227–39. doi:10.1002/ajmg.c.31399. PMID 24888723. S2CID 24534275.
Stutterd CA, Brock S, Stouffs K, Fanjul-Fernandez M, Lockhart PJ, McGillivray G, Mandelstam S, Pope K, Delatycki MB, Jansen A, Leventer RJ (2021). "Genetic heterogeneity of polymicrogyria: study of 123 patients using deep sequencing". Brain Communications. 3 (1): fcaa221. doi:10.1093/braincomms/fcaa221. PMC 7878248. PMID 33604570.
Bhat, V; Girimaji, SC; Mohan, G; Arvinda, HR; Singhmar, P; Duvvari, MR; Kumar, A (Apr 15, 2011). "Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations". Clinical Genetics. 80 (6): 532–40. doi:10.1111/j.1399-0004.2011.01686.x. PMID 21496009. S2CID 45190332.
Murdock DR, Clark GD, Bainbridge MN, Newsham I, Wu YQ, Muzny DM, Cheung SW, Gibbs RA, Ramocki MB (2011). "Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria". Am J Med Genet A. 155 (9): 2071–2077. doi:10.1002/ajmg.a.34165. PMC 3616765. PMID 21834044.
Smith RS, Kenny CJ, Ganesh V, Jang A, Borges-Monroy R, Partlow JN, Hill RS, Shin T, Chen AY, Doan RN, Anttonen AK, Ignatius J, Medne L, Bönnemann CG, Hecht JL, Salonen O, Barkovich AJ, Poduri A, Wilke M, de Wit MCY, Mancini GMS, Sztriha L, Im K, Amrom D, Andermann E, Paetau R, Lehesjoki AE, Walsh CA, Lehtinen MK (2018). "Sodium Channel SCN3A (Na_V1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development". Neuron. 99 (5): 905–913.e7. doi:10.1016/j.neuron.2018.07.052. PMC 6226006. PMID 30146301.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Smith, RS; Walsh, CA (February 2020). "Ion Channel Functions in Early Brain Development". Trends in Neurosciences. 43 (2): 103–114. doi:10.1016/j.tins.2019.12.004. PMC 7092371. PMID 31959360.
Kato, Mitsuhiro (2015-01-01). "Genotype-phenotype correlation in neuronal migration disorders and cortical dysplasias". Frontiers in Neuroscience. 9: 181. doi:10.3389/fnins.2015.00181. ISSN 1662-4548. PMC 4439546. PMID 26052266.
Fry, Andrew E.; Fawcett, Katherine A.; Zelnik, Nathanel; Yuan, Hongjie; Thompson, Belinda A N.; Shemer-Meiri, Lilach; Cushion, Thomas D.; Mugalaasi, Hood; Sims, David; Stoodley, Neil; Chung, Seo-Kyung; Rees, Mark I.; Patel, Chirag V.; Brueton, Louise A.; Layet, Valérie; Giuliano, Fabienne; Kerr, Michael P.; Banne, Ehud; Meiner, Vardiella; Lerman-Sagie, Tally; Helbig, Katherine L.; Kofman, Laura H.; Knight, Kristin M.; Chen, Wenjuan; Kannan, Varun; Hu, Chun; Kusumoto, Hirofumi; Zhang, Jin; Swanger, Sharon A.; et al. (2018). "De novo mutations in GRIN1 cause extensive bilateral polymicrogyria". Brain. 141 (3): 698–712. doi:10.1093/brain/awx358. PMC 5837214. PMID 29365063.
Squier, Waney; Jansen, Anna (2014-01-01). "Polymicrogyria: pathology, fetal origins and mechanisms". Acta Neuropathologica Communications. 2: 80. doi:10.1186/s40478-014-0080-3. ISSN 2051-5960. PMC 4149230. PMID 25047116.
Wang, Doris D.; Knox, Renatta; Rolston, John D.; Englot, Dario J.; Barkovich, A. James; Tihan, Tarik; Auguste, Kurtis I.; Knowlton, Robert C.; Cornes, Susannah B.; Chang, Edward F. (2016). "Surgical management of medically refractory epilepsy in patients with polymicrogyria". Epilepsia. 57 (1): 151–161. doi:10.1111/epi.13264. PMC 5237579. PMID 26647903.
Barkovich, A. James (2010-06-01). "Current concepts of polymicrogyria". Neuroradiology. 52 (6): 479–487. doi:10.1007/s00234-009-0644-2. ISSN 1432-1920. PMC 2872023. PMID 20198472.

nih.gov

pubmed.ncbi.nlm.nih.gov

Leventer RJ, Jansen A, Pilz DT, Stoodley N, Marini C, Dubeau F, Malone J, Mitchell LA, Mandelstam S, Scheffer IE, Berkovic SF, Andermann F, Andermann E, Guerrini R, Dobyns WB (May 2010). "Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients". Brain: A Journal of Neurology. 133 (Pt 5): 1415–27. doi:10.1093/brain/awq078. PMC 2859156. PMID 20403963.
Jansen, A.; Andermann, E. (1 May 2005). "Genetics of the polymicrogyria syndromes". Journal of Medical Genetics. 42 (5): 369–378. doi:10.1136/jmg.2004.023952. PMC 1736054. PMID 15863665.
Smith, RS; Kenny, CJ; Ganesh, V; Jang, A; Borges-Monroy, R; Partlow, JN; Hill, RS; Shin, T; Chen, AY; Doan, RN; Anttonen, AK; Ignatius, J; Medne, L; Bönnemann, CG; Hecht, JL; Salonen, O; Barkovich, AJ; Poduri, A; Wilke, M; de Wit, MCY; Mancini, GMS; Sztriha, L; Im, K; Amrom, D; Andermann, E; Paetau, R; Lehesjoki, AE; Walsh, CA; Lehtinen, MK (5 September 2018). "Sodium Channel SCN3A (Na_V1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development". Neuron. 99 (5): 905–913.e7. doi:10.1016/j.neuron.2018.07.052. PMC 6226006. PMID 30146301.
Stutterd CA, Leventer RJ (June 2014). "Polymicrogyria: a common and heterogeneous malformation of cortical development". Am J Med Genet C Semin Med Genet. 166C (2): 227–39. doi:10.1002/ajmg.c.31399. PMID 24888723. S2CID 24534275.
Stutterd, CA; Dobyns, WB; Jansen, A; Mirzaa, G; Leventer, RJ (1993–2022). Polymicrogyria Overview. Seattle, US: GeneReviews. PMID 20301504. Retrieved 3 April 2022.
Stutterd CA, Brock S, Stouffs K, Fanjul-Fernandez M, Lockhart PJ, McGillivray G, Mandelstam S, Pope K, Delatycki MB, Jansen A, Leventer RJ (2021). "Genetic heterogeneity of polymicrogyria: study of 123 patients using deep sequencing". Brain Communications. 3 (1): fcaa221. doi:10.1093/braincomms/fcaa221. PMC 7878248. PMID 33604570.
Bhat, V; Girimaji, SC; Mohan, G; Arvinda, HR; Singhmar, P; Duvvari, MR; Kumar, A (Apr 15, 2011). "Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations". Clinical Genetics. 80 (6): 532–40. doi:10.1111/j.1399-0004.2011.01686.x. PMID 21496009. S2CID 45190332.
Murdock DR, Clark GD, Bainbridge MN, Newsham I, Wu YQ, Muzny DM, Cheung SW, Gibbs RA, Ramocki MB (2011). "Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria". Am J Med Genet A. 155 (9): 2071–2077. doi:10.1002/ajmg.a.34165. PMC 3616765. PMID 21834044.
Smith RS, Kenny CJ, Ganesh V, Jang A, Borges-Monroy R, Partlow JN, Hill RS, Shin T, Chen AY, Doan RN, Anttonen AK, Ignatius J, Medne L, Bönnemann CG, Hecht JL, Salonen O, Barkovich AJ, Poduri A, Wilke M, de Wit MCY, Mancini GMS, Sztriha L, Im K, Amrom D, Andermann E, Paetau R, Lehesjoki AE, Walsh CA, Lehtinen MK (2018). "Sodium Channel SCN3A (Na_V1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development". Neuron. 99 (5): 905–913.e7. doi:10.1016/j.neuron.2018.07.052. PMC 6226006. PMID 30146301.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Smith, RS; Walsh, CA (February 2020). "Ion Channel Functions in Early Brain Development". Trends in Neurosciences. 43 (2): 103–114. doi:10.1016/j.tins.2019.12.004. PMC 7092371. PMID 31959360.
Kato, Mitsuhiro (2015-01-01). "Genotype-phenotype correlation in neuronal migration disorders and cortical dysplasias". Frontiers in Neuroscience. 9: 181. doi:10.3389/fnins.2015.00181. ISSN 1662-4548. PMC 4439546. PMID 26052266.
Fry, Andrew E.; Fawcett, Katherine A.; Zelnik, Nathanel; Yuan, Hongjie; Thompson, Belinda A N.; Shemer-Meiri, Lilach; Cushion, Thomas D.; Mugalaasi, Hood; Sims, David; Stoodley, Neil; Chung, Seo-Kyung; Rees, Mark I.; Patel, Chirag V.; Brueton, Louise A.; Layet, Valérie; Giuliano, Fabienne; Kerr, Michael P.; Banne, Ehud; Meiner, Vardiella; Lerman-Sagie, Tally; Helbig, Katherine L.; Kofman, Laura H.; Knight, Kristin M.; Chen, Wenjuan; Kannan, Varun; Hu, Chun; Kusumoto, Hirofumi; Zhang, Jin; Swanger, Sharon A.; et al. (2018). "De novo mutations in GRIN1 cause extensive bilateral polymicrogyria". Brain. 141 (3): 698–712. doi:10.1093/brain/awx358. PMC 5837214. PMID 29365063.
Chang, Bernard; Walsh, Christopher A.; Apse, Kira; Bodell, Adria (1993-01-01). Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora J.H.; Bird, Thomas D.; Fong, Chin-To; Mefford, Heather C. (eds.). Polymicrogyria Overview. Seattle (WA): University of Washington, Seattle. PMID 20301504.
Squier, Waney; Jansen, Anna (2014-01-01). "Polymicrogyria: pathology, fetal origins and mechanisms". Acta Neuropathologica Communications. 2: 80. doi:10.1186/s40478-014-0080-3. ISSN 2051-5960. PMC 4149230. PMID 25047116.
Wang, Doris D.; Knox, Renatta; Rolston, John D.; Englot, Dario J.; Barkovich, A. James; Tihan, Tarik; Auguste, Kurtis I.; Knowlton, Robert C.; Cornes, Susannah B.; Chang, Edward F. (2016). "Surgical management of medically refractory epilepsy in patients with polymicrogyria". Epilepsia. 57 (1): 151–161. doi:10.1111/epi.13264. PMC 5237579. PMID 26647903.
Barkovich, A. James (2010-06-01). "Current concepts of polymicrogyria". Neuroradiology. 52 (6): 479–487. doi:10.1007/s00234-009-0644-2. ISSN 1432-1920. PMC 2872023. PMID 20198472.

ncbi.nlm.nih.gov

Leventer RJ, Jansen A, Pilz DT, Stoodley N, Marini C, Dubeau F, Malone J, Mitchell LA, Mandelstam S, Scheffer IE, Berkovic SF, Andermann F, Andermann E, Guerrini R, Dobyns WB (May 2010). "Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients". Brain: A Journal of Neurology. 133 (Pt 5): 1415–27. doi:10.1093/brain/awq078. PMC 2859156. PMID 20403963.
Jansen, A.; Andermann, E. (1 May 2005). "Genetics of the polymicrogyria syndromes". Journal of Medical Genetics. 42 (5): 369–378. doi:10.1136/jmg.2004.023952. PMC 1736054. PMID 15863665.
Smith, RS; Kenny, CJ; Ganesh, V; Jang, A; Borges-Monroy, R; Partlow, JN; Hill, RS; Shin, T; Chen, AY; Doan, RN; Anttonen, AK; Ignatius, J; Medne, L; Bönnemann, CG; Hecht, JL; Salonen, O; Barkovich, AJ; Poduri, A; Wilke, M; de Wit, MCY; Mancini, GMS; Sztriha, L; Im, K; Amrom, D; Andermann, E; Paetau, R; Lehesjoki, AE; Walsh, CA; Lehtinen, MK (5 September 2018). "Sodium Channel SCN3A (Na_V1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development". Neuron. 99 (5): 905–913.e7. doi:10.1016/j.neuron.2018.07.052. PMC 6226006. PMID 30146301.
Stutterd, CA; Dobyns, WB; Jansen, A; Mirzaa, G; Leventer, RJ (1993–2022). Polymicrogyria Overview. Seattle, US: GeneReviews. PMID 20301504. Retrieved 3 April 2022.
Stutterd CA, Brock S, Stouffs K, Fanjul-Fernandez M, Lockhart PJ, McGillivray G, Mandelstam S, Pope K, Delatycki MB, Jansen A, Leventer RJ (2021). "Genetic heterogeneity of polymicrogyria: study of 123 patients using deep sequencing". Brain Communications. 3 (1): fcaa221. doi:10.1093/braincomms/fcaa221. PMC 7878248. PMID 33604570.
Murdock DR, Clark GD, Bainbridge MN, Newsham I, Wu YQ, Muzny DM, Cheung SW, Gibbs RA, Ramocki MB (2011). "Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria". Am J Med Genet A. 155 (9): 2071–2077. doi:10.1002/ajmg.a.34165. PMC 3616765. PMID 21834044.
Smith RS, Kenny CJ, Ganesh V, Jang A, Borges-Monroy R, Partlow JN, Hill RS, Shin T, Chen AY, Doan RN, Anttonen AK, Ignatius J, Medne L, Bönnemann CG, Hecht JL, Salonen O, Barkovich AJ, Poduri A, Wilke M, de Wit MCY, Mancini GMS, Sztriha L, Im K, Amrom D, Andermann E, Paetau R, Lehesjoki AE, Walsh CA, Lehtinen MK (2018). "Sodium Channel SCN3A (Na_V1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development". Neuron. 99 (5): 905–913.e7. doi:10.1016/j.neuron.2018.07.052. PMC 6226006. PMID 30146301.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Smith, RS; Walsh, CA (February 2020). "Ion Channel Functions in Early Brain Development". Trends in Neurosciences. 43 (2): 103–114. doi:10.1016/j.tins.2019.12.004. PMC 7092371. PMID 31959360.
Kato, Mitsuhiro (2015-01-01). "Genotype-phenotype correlation in neuronal migration disorders and cortical dysplasias". Frontiers in Neuroscience. 9: 181. doi:10.3389/fnins.2015.00181. ISSN 1662-4548. PMC 4439546. PMID 26052266.
Fry, Andrew E.; Fawcett, Katherine A.; Zelnik, Nathanel; Yuan, Hongjie; Thompson, Belinda A N.; Shemer-Meiri, Lilach; Cushion, Thomas D.; Mugalaasi, Hood; Sims, David; Stoodley, Neil; Chung, Seo-Kyung; Rees, Mark I.; Patel, Chirag V.; Brueton, Louise A.; Layet, Valérie; Giuliano, Fabienne; Kerr, Michael P.; Banne, Ehud; Meiner, Vardiella; Lerman-Sagie, Tally; Helbig, Katherine L.; Kofman, Laura H.; Knight, Kristin M.; Chen, Wenjuan; Kannan, Varun; Hu, Chun; Kusumoto, Hirofumi; Zhang, Jin; Swanger, Sharon A.; et al. (2018). "De novo mutations in GRIN1 cause extensive bilateral polymicrogyria". Brain. 141 (3): 698–712. doi:10.1093/brain/awx358. PMC 5837214. PMID 29365063.
Chang, Bernard; Walsh, Christopher A.; Apse, Kira; Bodell, Adria (1993-01-01). Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora J.H.; Bird, Thomas D.; Fong, Chin-To; Mefford, Heather C. (eds.). Polymicrogyria Overview. Seattle (WA): University of Washington, Seattle. PMID 20301504.
Squier, Waney; Jansen, Anna (2014-01-01). "Polymicrogyria: pathology, fetal origins and mechanisms". Acta Neuropathologica Communications. 2: 80. doi:10.1186/s40478-014-0080-3. ISSN 2051-5960. PMC 4149230. PMID 25047116.
Wang, Doris D.; Knox, Renatta; Rolston, John D.; Englot, Dario J.; Barkovich, A. James; Tihan, Tarik; Auguste, Kurtis I.; Knowlton, Robert C.; Cornes, Susannah B.; Chang, Edward F. (2016). "Surgical management of medically refractory epilepsy in patients with polymicrogyria". Epilepsia. 57 (1): 151–161. doi:10.1111/epi.13264. PMC 5237579. PMID 26647903.
Barkovich, A. James (2010-06-01). "Current concepts of polymicrogyria". Neuroradiology. 52 (6): 479–487. doi:10.1007/s00234-009-0644-2. ISSN 1432-1920. PMC 2872023. PMID 20198472.

orpha.net

Villard, Laurent (August 2004) [October 2002], "Polymicrogyria" (PDF), Orphanet Encyclopedia, Orphanet

semanticscholar.org

api.semanticscholar.org

Stutterd CA, Leventer RJ (June 2014). "Polymicrogyria: a common and heterogeneous malformation of cortical development". Am J Med Genet C Semin Med Genet. 166C (2): 227–39. doi:10.1002/ajmg.c.31399. PMID 24888723. S2CID 24534275.
Bhat, V; Girimaji, SC; Mohan, G; Arvinda, HR; Singhmar, P; Duvvari, MR; Kumar, A (Apr 15, 2011). "Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations". Clinical Genetics. 80 (6): 532–40. doi:10.1111/j.1399-0004.2011.01686.x. PMID 21496009. S2CID 45190332.

worldcat.org

search.worldcat.org

Kato, Mitsuhiro (2015-01-01). "Genotype-phenotype correlation in neuronal migration disorders and cortical dysplasias". Frontiers in Neuroscience. 9: 181. doi:10.3389/fnins.2015.00181. ISSN 1662-4548. PMC 4439546. PMID 26052266.
Squier, Waney; Jansen, Anna (2014-01-01). "Polymicrogyria: pathology, fetal origins and mechanisms". Acta Neuropathologica Communications. 2: 80. doi:10.1186/s40478-014-0080-3. ISSN 2051-5960. PMC 4149230. PMID 25047116.
Barkovich, A. James (2010-06-01). "Current concepts of polymicrogyria". Neuroradiology. 52 (6): 479–487. doi:10.1007/s00234-009-0644-2. ISSN 1432-1920. PMC 2872023. PMID 20198472.