260 related articles for article (PubMed ID: 22085975)
1. 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]
2. Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.
Hochstenbach R; Buizer-Voskamp JE; Vorstman JA; Ophoff RA
Cytogenet Genome Res; 2011; 135(3-4):174-202. PubMed ID: 22056632
[TBL] [Abstract][Full Text] [Related]
3. The role of DNA copy number variation in schizophrenia.
Tam GW; Redon R; Carter NP; Grant SG
Biol Psychiatry; 2009 Dec; 66(11):1005-12. PubMed ID: 19748074
[TBL] [Abstract][Full Text] [Related]
4. Recent genomic advances in schizophrenia.
Doherty JL; O'Donovan MC; Owen MJ
Clin Genet; 2012 Feb; 81(2):103-9. PubMed ID: 21895634
[TBL] [Abstract][Full Text] [Related]
5. Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.
Weiss LA
Expert Rev Mol Diagn; 2009 Nov; 9(8):795-803. PubMed ID: 19895225
[TBL] [Abstract][Full Text] [Related]
6. Copy-number variants in neurodevelopmental disorders: promises and challenges.
Merikangas AK; Corvin AP; Gallagher L
Trends Genet; 2009 Dec; 25(12):536-44. PubMed ID: 19910074
[TBL] [Abstract][Full Text] [Related]
7. Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?
Hosak L; Silhan P; Hosakova J
Neuro Endocrinol Lett; 2012; 33(2):183-90. PubMed ID: 22592199
[TBL] [Abstract][Full Text] [Related]
8. Microdeletion and microduplication syndromes.
Vissers LE; Stankiewicz P
Methods Mol Biol; 2012; 838():29-75. PubMed ID: 22228006
[TBL] [Abstract][Full Text] [Related]
9. Detection and characterization of copy number variation in autism spectrum disorder.
Marshall CR; Scherer SW
Methods Mol Biol; 2012; 838():115-35. PubMed ID: 22228009
[TBL] [Abstract][Full Text] [Related]
10. Copy number variations in neurodevelopmental disorders.
Grayton HM; Fernandes C; Rujescu D; Collier DA
Prog Neurobiol; 2012 Oct; 99(1):81-91. PubMed ID: 22813947
[TBL] [Abstract][Full Text] [Related]
11. Copy number variation and psychiatric disease risk.
Levy RJ; Xu B; Gogos JA; Karayiorgou M
Methods Mol Biol; 2012; 838():97-113. PubMed ID: 22228008
[TBL] [Abstract][Full Text] [Related]
12. Somatic cell genomics of brain disorders: a new opportunity to clarify genetic-environmental interactions.
Iourov IY; Vorsanova SG; Yurov YB
Cytogenet Genome Res; 2013; 139(3):181-8. PubMed ID: 23428498
[TBL] [Abstract][Full Text] [Related]
13. Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization.
Cho SC; Yim SH; Yoo HK; Kim MY; Jung GY; Shin GW; Kim BN; Hwang JW; Kang JJ; Kim TM; Chung YJ
Psychiatr Genet; 2009 Aug; 19(4):177-85. PubMed ID: 19407672
[TBL] [Abstract][Full Text] [Related]
14. New technologies provide insights into genetic basis of psychiatric disorders and explain their co-morbidity.
Rudan I
Psychiatr Danub; 2010 Jun; 22(2):190-2. PubMed ID: 20562745
[TBL] [Abstract][Full Text] [Related]
15. Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes.
Mulley JC; Scheffer IE; Desai T; Bayly MA; Grinton BE; Vears DF; Berkovic SF; Dibbens LM
Epilepsia; 2011 Oct; 52(10):e139-42. PubMed ID: 21777232
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Ohnologs are overrepresented in pathogenic copy number mutations.
McLysaght A; Makino T; Grayton HM; Tropeano M; Mitchell KJ; Vassos E; Collier DA
Proc Natl Acad Sci U S A; 2014 Jan; 111(1):361-6. PubMed ID: 24368850
[TBL] [Abstract][Full Text] [Related]
18. Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree.
Lesch KP; Selch S; Renner TJ; Jacob C; Nguyen TT; Hahn T; Romanos M; Walitza S; Shoichet S; Dempfle A; Heine M; Boreatti-Hümmer A; Romanos J; Gross-Lesch S; Zerlaut H; Wultsch T; Heinzel S; Fassnacht M; Fallgatter A; Allolio B; Schäfer H; Warnke A; Reif A; Ropers HH; Ullmann R
Mol Psychiatry; 2011 May; 16(5):491-503. PubMed ID: 20308990
[TBL] [Abstract][Full Text] [Related]
19. Genome wide analysis of novel copy number variations duplications/deletions of different epileptic patients in Saudi Arabia.
Naseer MI; Faheem M; Chaudhary AG; Kumosani TA; Al-Quaiti MM; Jan MM; Saleh Jamal H; Al-Qahtani MH
BMC Genomics; 2015; 16 Suppl 1(Suppl 1):S10. PubMed ID: 25923336
[TBL] [Abstract][Full Text] [Related]
20. Array comparative genomic hybridisation of 52 subjects with a Smith-Magenis-like phenotype: identification of dosage sensitive loci also associated with schizophrenia, autism, and developmental delay.
Williams SR; Girirajan S; Tegay D; Nowak N; Hatchwell E; Elsea SH
J Med Genet; 2010 Apr; 47(4):223-9. PubMed ID: 19752160
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
