Similar articles for PMID: 24625750

Year	Number of Results
2006	1
2008	3
2009	2
2010	7
2011	7
2012	5
2013	7
2014	8
2015	5
2016	8
2017	13
2018	10
2019	7
2020	8
2021	6
2022	4
2023	4
2024	0

1

Sequencing of a patient with balanced chromosome abnormalities and neurodevelopmental disease identifies disruption of multiple high risk loci by structural variation.

Blake J, Riddell A, Theiss S, Gonzalez AP, Haase B, Jauch A, Janssen JW, Ibberson D, Pavlinic D, Moog U, Benes V, Runz H. Blake J, et al. PLoS One. 2014 Mar 13;9(3):e90894. doi: 10.1371/journal.pone.0090894. eCollection 2014. PLoS One. 2014. PMID: 24625750 Free PMC article.

2

Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders.

Reuter MS, Tawamie H, Buchert R, Hosny Gebril O, Froukh T, Thiel C, Uebe S, Ekici AB, Krumbiegel M, Zweier C, Hoyer J, Eberlein K, Bauer J, Scheller U, Strom TM, Hoffjan S, Abdelraouf ER, Meguid NA, Abboud A, Al Khateeb MA, Fakher M, Hamdan S, Ismael A, Muhammad S, Abdallah E, Sticht H, Wieczorek D, Reis A, Abou Jamra R. Reuter MS, et al. JAMA Psychiatry. 2017 Mar 1;74(3):293-299. doi: 10.1001/jamapsychiatry.2016.3798. JAMA Psychiatry. 2017. PMID: 28097321

3

A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencing.

Dong Z, Jiang L, Yang C, Hu H, Wang X, Chen H, Choy KW, Hu H, Dong Y, Hu B, Xu J, Long Y, Cao S, Chen H, Wang WJ, Jiang H, Xu F, Yao H, Xu X, Liang Z. Dong Z, et al. Hum Mutat. 2014 May;35(5):625-36. doi: 10.1002/humu.22541. Epub 2014 Apr 9. Hum Mutat. 2014. PMID: 24610732

4

Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries.

Talkowski ME, Rosenfeld JA, Blumenthal I, Pillalamarri V, Chiang C, Heilbut A, Ernst C, Hanscom C, Rossin E, Lindgren AM, Pereira S, Ruderfer D, Kirby A, Ripke S, Harris DJ, Lee JH, Ha K, Kim HG, Solomon BD, Gropman AL, Lucente D, Sims K, Ohsumi TK, Borowsky ML, Loranger S, Quade B, Lage K, Miles J, Wu BL, Shen Y, Neale B, Shaffer LG, Daly MJ, Morton CC, Gusella JF. Talkowski ME, et al. Cell. 2012 Apr 27;149(3):525-37. doi: 10.1016/j.cell.2012.03.028. Epub 2012 Apr 19. Cell. 2012. PMID: 22521361 Free PMC article.

5

Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis.

Yu MHC, Chau JFT, Au SLK, Lo HM, Yeung KS, Fung JLF, Mak CCY, Chung CCY, Chan KYK, Chung BHY, Kan ASY. Yu MHC, et al. Front Genet. 2021 Jan 27;11:620162. doi: 10.3389/fgene.2020.620162. eCollection 2020. Front Genet. 2021. PMID: 33584815 Free PMC article.

6

A survey of undetected, clinically relevant chromosome abnormalities when replacing postnatal karyotyping by Whole Genome Sequencing.

Hochstenbach R, van Binsbergen E, Schuring-Blom H, Buijs A, Ploos van Amstel HK. Hochstenbach R, et al. Eur J Med Genet. 2019 Sep;62(9):103543. doi: 10.1016/j.ejmg.2018.09.010. Epub 2018 Sep 22. Eur J Med Genet. 2019. PMID: 30248410

7

Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.

Devanna P, Chen XS, Ho J, Gajewski D, Smith SD, Gialluisi A, Francks C, Fisher SE, Newbury DF, Vernes SC. Devanna P, et al. Mol Psychiatry. 2018 May;23(5):1375-1384. doi: 10.1038/mp.2017.30. Epub 2017 Mar 14. Mol Psychiatry. 2018. PMID: 28289279 Free PMC article.

8

Bioinformatic analyses and conceptual synthesis of evidence linking ZNF804A to risk for schizophrenia and bipolar disorder.

Hess JL, Quinn TP, Akbarian S, Glatt SJ. Hess JL, et al. Am J Med Genet B Neuropsychiatr Genet. 2015 Jan;168B(1):14-35. doi: 10.1002/ajmg.b.32284. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 25522715 Review.

9

How might ZNF804A variants influence risk for schizophrenia and bipolar disorder? A literature review, synthesis, and bioinformatic analysis.

Hess JL, Glatt SJ. Hess JL, et al. Am J Med Genet B Neuropsychiatr Genet. 2014 Jan;165B(1):28-40. doi: 10.1002/ajmg.b.32207. Epub 2013 Oct 4. Am J Med Genet B Neuropsychiatr Genet. 2014. PMID: 24123948 Review.

10

Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research.

Talkowski ME, Ernst C, Heilbut A, Chiang C, Hanscom C, Lindgren A, Kirby A, Liu S, Muddukrishna B, Ohsumi TK, Shen Y, Borowsky M, Daly MJ, Morton CC, Gusella JF. Talkowski ME, et al. Am J Hum Genet. 2011 Apr 8;88(4):469-81. doi: 10.1016/j.ajhg.2011.03.013. Am J Hum Genet. 2011. PMID: 21473983 Free PMC article.

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