267 related articles for article (PubMed ID: 25923336)
21. Disentangling the myriad genomics of complex disorders, specifically focusing on autism, epilepsy, and schizophrenia.
Poot M; van der Smagt JJ; Brilstra EH; Bourgeron T
Cytogenet Genome Res; 2011; 135(3-4):228-40. PubMed ID: 22085975
[TBL] [Abstract][Full Text] [Related]
22. Clinical and molecular characterization of three genomic rearrangements at chromosome 22q13.3 associated with autism spectrum disorder.
Chen CH; Chen HI; Liao HM; Chen YJ; Fang JS; Lee KF; Gau SS
Psychiatr Genet; 2017 Feb; 27(1):23-33. PubMed ID: 27846046
[TBL] [Abstract][Full Text] [Related]
23. Screening chromosomal aberrations by array comparative genomic hybridization in 80 patients with congenital hypothyroidism and thyroid dysgenesis.
Thorwarth A; Mueller I; Biebermann H; Ropers HH; Grueters A; Krude H; Ullmann R
J Clin Endocrinol Metab; 2010 Jul; 95(7):3446-52. PubMed ID: 20427504
[TBL] [Abstract][Full Text] [Related]
24. Assessment of copy number variations in 120 patients with Poland syndrome.
Vaccari CM; Tassano E; Torre M; Gimelli S; Divizia MT; Romanini MV; Bossi S; Musante I; Valle M; Senes F; Catena N; Bedeschi MF; Baban A; Calevo MG; Acquaviva M; Lerone M; Ravazzolo R; Puliti A
BMC Med Genet; 2016 Nov; 17(1):89. PubMed ID: 27884122
[TBL] [Abstract][Full Text] [Related]
25. High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy.
Stewart LR; Hall AL; Kang SH; Shaw CA; Beaudet AL
BMC Med Genet; 2011 Nov; 12():154. PubMed ID: 22118685
[TBL] [Abstract][Full Text] [Related]
26. Molecular Karyotyping of a Dysmorphic Girl from Saudi Arabia with CYP1B1-negative Primary Congenital Glaucoma.
Abu-Amero KK; Kondkar AA; Khan AO
Ophthalmic Genet; 2016; 37(1):98-101. PubMed ID: 24911043
[TBL] [Abstract][Full Text] [Related]
27. Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.
Niestroj LM; Perez-Palma E; Howrigan DP; Zhou Y; Cheng F; Saarentaus E; Nürnberg P; Stevelink R; Daly MJ; Palotie A; Lal D;
Brain; 2020 Jul; 143(7):2106-2118. PubMed ID: 32568404
[TBL] [Abstract][Full Text] [Related]
28. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways.
Canton AP; Costa SS; Rodrigues TC; Bertola DR; Malaquias AC; Correa FA; Arnhold IJ; Rosenberg C; Jorge AA
Eur J Endocrinol; 2014 Aug; 171(2):253-62. PubMed ID: 24878679
[TBL] [Abstract][Full Text] [Related]
29. Epilepsy and the new cytogenetics.
Mulley JC; Mefford HC
Epilepsia; 2011 Mar; 52(3):423-32. PubMed ID: 21269290
[TBL] [Abstract][Full Text] [Related]
30. Impact of copy number variants in epilepsy plus neurodevelopment disorders.
João S; Quental R; Pinto J; Almeida C; Santos H; Dória S
Seizure; 2024 Apr; 117():6-12. PubMed ID: 38277927
[TBL] [Abstract][Full Text] [Related]
31. Genome-wide patterns of copy number variation in the diversified chicken genomes using next-generation sequencing.
Yi G; Qu L; Liu J; Yan Y; Xu G; Yang N
BMC Genomics; 2014 Nov; 15(1):962. PubMed ID: 25378104
[TBL] [Abstract][Full Text] [Related]
32. Altered DNA copy number in patients with different seizure disorder type: by array-CGH.
Kim HS; Yim SV; Jung KH; Zheng LT; Kim YH; Lee KH; Chung SY; Rha HK
Brain Dev; 2007 Nov; 29(10):639-43. PubMed ID: 17573221
[TBL] [Abstract][Full Text] [Related]
33. The unexpected role of copy number variations in juvenile myoclonic epilepsy.
Helbig I; Hartmann C; Mefford HC
Epilepsy Behav; 2013 Jul; 28 Suppl 1():S66-8. PubMed ID: 23756484
[TBL] [Abstract][Full Text] [Related]
34. Copy number variants in adult patients with Lennox-Gastaut syndrome features.
Lund C; Brodtkorb E; Røsby O; Rødningen OK; Selmer KK
Epilepsy Res; 2013 Jul; 105(1-2):110-7. PubMed ID: 23415449
[TBL] [Abstract][Full Text] [Related]
35. Intragenic rearrangements in X-linked intellectual deficiency: results of a-CGH in a series of 54 patients and identification of TRPC5 and KLHL15 as potential XLID genes.
Mignon-Ravix C; Cacciagli P; Choucair N; Popovici C; Missirian C; Milh M; Mégarbané A; Busa T; Julia S; Girard N; Badens C; Sigaudy S; Philip N; Villard L
Am J Med Genet A; 2014 Aug; 164A(8):1991-7. PubMed ID: 24817631
[TBL] [Abstract][Full Text] [Related]
36. Case history and genome-wide scans for copy number variants in a family with patient having 15q11.1-q11.2 duplication and 22q11.2 deletion, and schizophrenia.
Takahashi S; Suzuki T; Nakamura-Tomizuka S; Osaki K; Sotome Y; Sagawa T; Uchiyama M
Am J Med Genet B Neuropsychiatr Genet; 2015 Jun; 168B(4):229-35. PubMed ID: 25776014
[TBL] [Abstract][Full Text] [Related]
37. Refining the Phenotype of Recurrent Rearrangements of Chromosome 16.
Redaelli S; Maitz S; Crosti F; Sala E; Villa N; Spaccini L; Selicorni A; Rigoldi M; Conconi D; Dalprà L; Roversi G; Bentivegna A
Int J Mol Sci; 2019 Mar; 20(5):. PubMed ID: 30836598
[TBL] [Abstract][Full Text] [Related]
38. Copy number variation analysis in adults with catatonia confirms haploinsufficiency of SHANK3 as a predisposing factor.
Breckpot J; Vercruyssen M; Weyts E; Vandevoort S; D'Haenens G; Van Buggenhout G; Leempoels L; Brischoux-Boucher E; Van Maldergem L; Renieri A; Mencarelli MA; D'Angelo C; Mericq V; Hoffer MJ; Tauber M; Molinas C; Castiglioni C; Brison N; Vermeesch JR; Danckaerts M; Sienaert P; Devriendt K; Vogels A
Eur J Med Genet; 2016 Sep; 59(9):436-43. PubMed ID: 27519580
[TBL] [Abstract][Full Text] [Related]
39. Genetic predisposition in degenerative lumbar scoliosis due to the copy number variation.
Shin JH; Ha KY; Jung SH; Chung YJ
Spine (Phila Pa 1976); 2011 Oct; 36(21):1782-93. PubMed ID: 21587107
[TBL] [Abstract][Full Text] [Related]
40. Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes.
Rosenfeld JA; Traylor RN; Schaefer GB; McPherson EW; Ballif BC; Klopocki E; Mundlos S; Shaffer LG; Aylsworth AS;
Eur J Hum Genet; 2012 Jul; 20(7):754-61. PubMed ID: 22317977
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]