249 related articles for article (PubMed ID: 28771244)
1. De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy.
Zarrei M; Fehlings DL; Mawjee K; Switzer L; Thiruvahindrapuram B; Walker S; Merico D; Casallo G; Uddin M; MacDonald JR; Gazzellone MJ; Higginbotham EJ; Campbell C; deVeber G; Frid P; Gorter JW; Hunt C; Kawamura A; Kim M; McCormick A; Mesterman R; Samdup D; Marshall CR; Stavropoulos DJ; Wintle RF; Scherer SW
Genet Med; 2018 Feb; 20(2):172-180. PubMed ID: 28771244
[TBL] [Abstract][Full Text] [Related]
2. Clinically relevant copy number variations detected in cerebral palsy.
Oskoui M; Gazzellone MJ; Thiruvahindrapuram B; Zarrei M; Andersen J; Wei J; Wang Z; Wintle RF; Marshall CR; Cohn RD; Weksberg R; Stavropoulos DJ; Fehlings D; Shevell MI; Scherer SW
Nat Commun; 2015 Aug; 6():7949. PubMed ID: 26236009
[TBL] [Abstract][Full Text] [Related]
3. Cerebral palsy and related neuromotor disorders: Overview of genetic and genomic studies.
Friedman JM; van Essen P; van Karnebeek CDM
Mol Genet Metab; 2022 Dec; 137(4):399-419. PubMed ID: 34872807
[TBL] [Abstract][Full Text] [Related]
4. Copy number variations in cryptogenic cerebral palsy.
Segel R; Ben-Pazi H; Zeligson S; Fatal-Valevski A; Aran A; Gross-Tsur V; Schneebaum-Sender N; Shmueli D; Lev D; Perlberg S; Blumkin L; Deutsch L; Levy-Lahad E
Neurology; 2015 Apr; 84(16):1660-8. PubMed ID: 25817843
[TBL] [Abstract][Full Text] [Related]
5. The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease.
Warburton D; Ronemus M; Kline J; Jobanputra V; Williams I; Anyane-Yeboa K; Chung W; Yu L; Wong N; Awad D; Yu CY; Leotta A; Kendall J; Yamrom B; Lee YH; Wigler M; Levy D
Hum Genet; 2014 Jan; 133(1):11-27. PubMed ID: 23979609
[TBL] [Abstract][Full Text] [Related]
6. Clinical significance of de novo and inherited copy-number variation.
Vulto-van Silfhout AT; Hehir-Kwa JY; van Bon BW; Schuurs-Hoeijmakers JH; Meader S; Hellebrekers CJ; Thoonen IJ; de Brouwer AP; Brunner HG; Webber C; Pfundt R; de Leeuw N; de Vries BB
Hum Mutat; 2013 Dec; 34(12):1679-87. PubMed ID: 24038936
[TBL] [Abstract][Full Text] [Related]
7. Rare copy number variation in cerebral palsy.
McMichael G; Girirajan S; Moreno-De-Luca A; Gecz J; Shard C; Nguyen LS; Nicholl J; Gibson C; Haan E; Eichler E; Martin CL; MacLennan A
Eur J Hum Genet; 2014 Jan; 22(1):40-5. PubMed ID: 23695280
[TBL] [Abstract][Full Text] [Related]
8. Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.
Lionel AC; Crosbie J; Barbosa N; Goodale T; Thiruvahindrapuram B; Rickaby J; Gazzellone M; Carson AR; Howe JL; Wang Z; Wei J; Stewart AF; Roberts R; McPherson R; Fiebig A; Franke A; Schreiber S; Zwaigenbaum L; Fernandez BA; Roberts W; Arnold PD; Szatmari P; Marshall CR; Schachar R; Scherer SW
Sci Transl Med; 2011 Aug; 3(95):95ra75. PubMed ID: 21832240
[TBL] [Abstract][Full Text] [Related]
9. Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsy.
Yechieli M; Gulsuner S; Ben-Pazi H; Fattal A; Aran A; Kuzminsky A; Sagi L; Guttman D; Schneebaum Sender N; Gross-Tsur V; Klopstock T; Walsh T; Renbaum P; Zeligson S; Shemer Meiri L; Lev D; Shmueli D; Blumkin L; Lahad A; King MC; Levy EL; Segel R
J Med Genet; 2022 Aug; 59(8):759-767. PubMed ID: 34321325
[TBL] [Abstract][Full Text] [Related]
10. Rare de novo copy number variants in patients with congenital pulmonary atresia.
Xie L; Chen JL; Zhang WZ; Wang SZ; Zhao TL; Huang C; Wang J; Yang JF; Yang YF; Tan ZP
PLoS One; 2014; 9(5):e96471. PubMed ID: 24826987
[TBL] [Abstract][Full Text] [Related]
11. De novo CNVs in bipolar affective disorder and schizophrenia.
Georgieva L; Rees E; Moran JL; Chambert KD; Milanova V; Craddock N; Purcell S; Sklar P; McCarroll S; Holmans P; O'Donovan MC; Owen MJ; Kirov G
Hum Mol Genet; 2014 Dec; 23(24):6677-83. PubMed ID: 25055870
[TBL] [Abstract][Full Text] [Related]
12. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
Kirov G; Pocklington AJ; Holmans P; Ivanov D; Ikeda M; Ruderfer D; Moran J; Chambert K; Toncheva D; Georgieva L; Grozeva D; Fjodorova M; Wollerton R; Rees E; Nikolov I; van de Lagemaat LN; Bayés A; Fernandez E; Olason PI; Böttcher Y; Komiyama NH; Collins MO; Choudhary J; Stefansson K; Stefansson H; Grant SG; Purcell S; Sklar P; O'Donovan MC; Owen MJ
Mol Psychiatry; 2012 Feb; 17(2):142-53. PubMed ID: 22083728
[TBL] [Abstract][Full Text] [Related]
13. Hemiplegic cerebral palsy and the factor V Leiden mutation.
Halliday JL; Reddihough D; Byron K; Ekert H; Ditchfield M
J Med Genet; 2000 Oct; 37(10):787-9. PubMed ID: 11183183
[No Abstract] [Full Text] [Related]
14. Copy-number variations are enriched for neurodevelopmental genes in children with developmental coordination disorder.
Mosca SJ; Langevin LM; Dewey D; Innes AM; Lionel AC; Marshall CC; Scherer SW; Parboosingh JS; Bernier FP
J Med Genet; 2016 Dec; 53(12):812-819. PubMed ID: 27489308
[TBL] [Abstract][Full Text] [Related]
15. Enrichment of rare copy number variation in children with developmental language disorder.
Kalnak N; Stamouli S; Peyrard-Janvid M; Rabkina I; Becker M; Klingberg T; Kere J; Forssberg H; Tammimies K
Clin Genet; 2018 Oct; 94(3-4):313-320. PubMed ID: 29851021
[TBL] [Abstract][Full Text] [Related]
16. Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.
Borlot F; Regan BM; Bassett AS; Stavropoulos DJ; Andrade DM
JAMA Neurol; 2017 Nov; 74(11):1301-1311. PubMed ID: 28846756
[TBL] [Abstract][Full Text] [Related]
17. Identification of novel candidate disease genes from de novo exonic copy number variants.
Gambin T; Yuan B; Bi W; Liu P; Rosenfeld JA; Coban-Akdemir Z; Pursley AN; Nagamani SCS; Marom R; Golla S; Dengle L; Petrie HG; Matalon R; Emrick L; Proud MB; Treadwell-Deering D; Chao HT; Koillinen H; Brown C; Urraca N; Mostafavi R; Bernes S; Roeder ER; Nugent KM; Bader PI; Bellus G; Cummings M; Northrup H; Ashfaq M; Westman R; Wildin R; Beck AE; Immken L; Elton L; Varghese S; Buchanan E; Faivre L; Lefebvre M; Schaaf CP; Walkiewicz M; Yang Y; Kang SL; Lalani SR; Bacino CA; Beaudet AL; Breman AM; Smith JL; Cheung SW; Lupski JR; Patel A; Shaw CA; Stankiewicz P
Genome Med; 2017 Sep; 9(1):83. PubMed ID: 28934986
[TBL] [Abstract][Full Text] [Related]
18. Exome sequencing reveals genetic heterogeneity and clinically actionable findings in children with cerebral palsy.
Wang Y; Xu Y; Zhou C; Cheng Y; Qiao N; Shang Q; Xia L; Song J; Gao C; Qiao Y; Zhang X; Li M; Ma C; Fan Y; Peng X; Wu S; Lv N; Li B; Sun Y; Zhang B; Li T; Li H; Zhang J; Su Y; Li Q; Yuan J; Liu L; Moreno-De-Luca A; MacLennan AH; Gecz J; Zhu D; Wang X; Zhu C; Xing Q
Nat Med; 2024 May; 30(5):1395-1405. PubMed ID: 38693247
[TBL] [Abstract][Full Text] [Related]
19. Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development.
Safizadeh Shabestari SA; Nassir N; Sopariwala S; Karimov I; Tambi R; Zehra B; Kosaji N; Akter H; Berdiev BK; Uddin M
Hum Genet; 2023 Aug; 142(8):1201-1213. PubMed ID: 36383254
[TBL] [Abstract][Full Text] [Related]
20. Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort.
da Silva Montenegro EM; Costa CS; Campos G; Scliar M; de Almeida TF; Zachi EC; Silva IMW; Chan AJS; Zarrei M; Lourenço NCV; Yamamoto GL; Scherer S; Passos-Bueno MR
Autism Res; 2020 Feb; 13(2):199-206. PubMed ID: 31696658
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]