Behar DM - Search Results

1

Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5.

Magen D, Ofir A, Berger L, Goldsher D, Eran A, Katib N, Nijem Y, Vlodavsky E, Tzur S, Behar DM, Fellig Y, Mandel H. Magen D, et al. Among authors: behar dm. Hum Genet. 2015 Mar;134(3):315. doi: 10.1007/s00439-015-1530-0. Hum Genet. 2015. PMID: 25609191 No abstract available.

2

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5.

Magen D, Ofir A, Berger L, Goldsher D, Eran A, Katib N, Nijem Y, Vlodavsky E, Tzur S, Behar DM, Fellig Y, Mandel H. Magen D, et al. Among authors: behar dm. Hum Genet. 2015 Mar;134(3):305-14. doi: 10.1007/s00439-014-1522-5. Epub 2015 Jan 6. Hum Genet. 2015. PMID: 25560765

3

Intellectual disability and non-compaction cardiomyopathy with a de novo NONO mutation identified by exome sequencing.

Reinstein E, Tzur S, Cohen R, Bormans C, Behar DM. Reinstein E, et al. Among authors: behar dm. Eur J Hum Genet. 2016 Nov;24(11):1635-1638. doi: 10.1038/ejhg.2016.72. Epub 2016 Jun 22. Eur J Hum Genet. 2016. PMID: 27329731 Free PMC article.

4

African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans.

Behar DM, Rosset S, Tzur S, Selig S, Yudkovsky G, Bercovici S, Kopp JB, Winkler CA, Nelson GW, Wasser WG, Skorecki K. Behar DM, et al. Hum Mol Genet. 2010 May 1;19(9):1816-27. doi: 10.1093/hmg/ddq040. Epub 2010 Feb 9. Hum Mol Genet. 2010. PMID: 20144966 Free PMC article.

5

Exome sequencing identified mutations in CASK and MYBPC3 as the cause of a complex dilated cardiomyopathy phenotype.

Reinstein E, Tzur S, Bormans C, Behar DM. Reinstein E, et al. Among authors: behar dm. Genet Res (Camb). 2016 May 13;98:e8. doi: 10.1017/S0016672316000045. Genet Res (Camb). 2016. PMID: 27173948 Free PMC article.

6

Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.

Tzur S, Rosset S, Shemer R, Yudkovsky G, Selig S, Tarekegn A, Bekele E, Bradman N, Wasser WG, Behar DM, Skorecki K. Tzur S, et al. Among authors: behar dm. Hum Genet. 2010 Sep;128(3):345-50. doi: 10.1007/s00439-010-0861-0. Epub 2010 Jul 16. Hum Genet. 2010. PMID: 20635188 Free PMC article.

7

The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder event.

Behar DM, Metspalu E, Kivisild T, Achilli A, Hadid Y, Tzur S, Pereira L, Amorim A, Quintana-Murci L, Majamaa K, Herrnstadt C, Howell N, Balanovsky O, Kutuev I, Pshenichnov A, Gurwitz D, Bonne-Tamir B, Torroni A, Villems R, Skorecki K. Behar DM, et al. Am J Hum Genet. 2006 Mar;78(3):487-97. doi: 10.1086/500307. Epub 2006 Jan 11. Am J Hum Genet. 2006. PMID: 16404693 Free PMC article.

8

Exome sequencing reveals SYCE1 mutation associated with autosomal recessive primary ovarian insufficiency.

de Vries L, Behar DM, Smirin-Yosef P, Lagovsky I, Tzur S, Basel-Vanagaite L. de Vries L, et al. Among authors: behar dm. J Clin Endocrinol Metab. 2014 Oct;99(10):E2129-32. doi: 10.1210/jc.2014-1268. Epub 2014 Jul 25. J Clin Endocrinol Metab. 2014. PMID: 25062452

9

Homozygous MED25 mutation implicated in eye-intellectual disability syndrome.

Basel-Vanagaite L, Smirin-Yosef P, Essakow JL, Tzur S, Lagovsky I, Maya I, Pasmanik-Chor M, Yeheskel A, Konen O, Orenstein N, Weisz Hubshman M, Drasinover V, Magal N, Peretz Amit G, Zalzstein Y, Zeharia A, Shohat M, Straussberg R, Monté D, Salmon-Divon M, Behar DM. Basel-Vanagaite L, et al. Among authors: behar dm. Hum Genet. 2015 Jun;134(6):577-87. doi: 10.1007/s00439-015-1541-x. Epub 2015 Mar 20. Hum Genet. 2015. PMID: 25792360 Clinical Trial.

10

The dawn of human matrilineal diversity.

Behar DM, Villems R, Soodyall H, Blue-Smith J, Pereira L, Metspalu E, Scozzari R, Makkan H, Tzur S, Comas D, Bertranpetit J, Quintana-Murci L, Tyler-Smith C, Wells RS, Rosset S; Genographic Consortium. Behar DM, et al. Am J Hum Genet. 2008 May;82(5):1130-40. doi: 10.1016/j.ajhg.2008.04.002. Epub 2008 Apr 24. Am J Hum Genet. 2008. PMID: 18439549 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

118 results

Search Page

Filters