Reish O - Search Results

1

Dynamic modification strategy of the Israeli carrier screening protocol: inclusion of the Oriental Jewish Group to the cystic fibrosis panel.

Reish O, Borochowitz ZU, Adir V, Shohat M, Karpati M, Shtorch A, Orr-Urtreger A, Yaron Y, Shalev S, Fares F, Gershoni-Baruch R, Falik-Zaccai TC, Chapman-Shimshoni D. Reish O, et al. Genet Med. 2009 Feb;11(2):101-3. doi: 10.1097/GIM.0b013e31818efd59. Genet Med. 2009. PMID: 19265749 Free article.

2

Dynamic modification strategy of the Israeli prenatal carrier screening protocol: inclusion of the oriental Jewish group to the cystic fibrosis panel-update.

Reish O, Shohat M, Magal N, Pesso R, Borochowitz ZU, Adir V, Karpati M, Shimshoni DC. Reish O, et al. Genet Med. 2009 May;11(5):372. doi: 10.1097/GIM.0b013e3181a02f04. Genet Med. 2009. PMID: 19346956 Free article. No abstract available.

3

Frequencies of C282Y and H63D alleles in the HFE gene among various Jewish ethnic groups in Israel: a change of concept required.

Reish O, Shefer-Kaufmann N, Shimshoni DC, Renbaum P, Orr-Urtreger A, Steiner H, Rapoport M, Levy-Lahad E, Altarescu G. Reish O, et al. Genet Med. 2010 Feb;12(2):122-5. doi: 10.1097/GIM.0b013e3181cb78d6. Genet Med. 2010. PMID: 20084012 Free article.

4

Prenatal diagnosis of Down syndrome: ten year experience in the Israeli population.

Shohat M, Frimer H, Shohat-Levy V, Esmailzadeh H, Appelman Z, Ben-Neriah Z, Dar H, Orr-Urtreger A, Amiel A, Gershoni R, Manor E, Barkai G, Shalev S, Gelman-Kohen Z, Reish O, Lev D, Davidov B, Goldman B. Shohat M, et al. Among authors: reish o. Am J Med Genet A. 2003 Oct 15;122A(3):215-22. doi: 10.1002/ajmg.a.20246. Am J Med Genet A. 2003. PMID: 12966521

5

Founder mutation(s) in the RSPH9 gene leading to primary ciliary dyskinesia in two inbred Bedouin families.

Reish O, Slatkin M, Chapman-Shimshoni D, Elizur A, Chioza B, Castleman V, Mitchison HM. Reish O, et al. Ann Hum Genet. 2010 Mar;74(2):117-25. doi: 10.1111/j.1469-1809.2009.00559.x. Epub 2010 Jan 8. Ann Hum Genet. 2010. PMID: 20070851 Free PMC article.

6

Mosaic compound heterozygosity of SHOX resulting in Leri-Weill dyschondrosteosis with marked short stature: implications for disease mechanisms and recurrence risks.

Reish O, Huber C, Altarescu G, Chapman-Shimshoni D, Levy-Lahad E, Renbaum P, Mashevich M, Munnich A, Cormier-Daire V. Reish O, et al. Am J Med Genet A. 2010 Sep;152A(9):2230-5. doi: 10.1002/ajmg.a.33563. Am J Med Genet A. 2010. PMID: 20683993

7

Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel.

Yablonski-Peretz T, Paluch-Shimon S, Gutman LS, Kaplan Y, Dvir A, Barnes-Kedar I, Kadouri L, Semenisty V, Efrat N, Neiman V, Glasser Y, Michaelson-Cohen R, Katz L, Kaufman B, Golan T, Reish O, Hubert A, Safra T, Yaron Y, Friedman E. Yablonski-Peretz T, et al. Among authors: reish o. Breast Cancer Res Treat. 2016 Jan;155(1):133-8. doi: 10.1007/s10549-015-3662-2. Epub 2015 Dec 19. Breast Cancer Res Treat. 2016. PMID: 26687385

8

Molecular analysis of an extended Palestinian family from Israel with monilethrix.

Oetting WS, Fryer JP, Wyman Z, Shtorch A, Cordoba M, Lazarov A, Reish O. Oetting WS, et al. Among authors: reish o. Genet Med. 1999 Mar-Apr;1(3):109-11. doi: 10.1097/00125817-199903000-00009. Genet Med. 1999. PMID: 11336449 Free article.

9

Chromosome aberration and environmental physical activity: Down syndrome and solar and cosmic ray activity, Israel, 1990-2000.

Stoupel EG, Frimer H, Appelman Z, Ben-Neriah Z, Dar H, Fejgin MD, Gershoni-Baruch R, Manor E, Barkai G, Shalev S, Gelman-Kohan Z, Reish O, Lev D, Davidov B, Goldman B, Shohat M. Stoupel EG, et al. Among authors: reish o. Int J Biometeorol. 2005 Sep;50(1):1-5. doi: 10.1007/s00484-005-0274-2. Epub 2005 Jun 30. Int J Biometeorol. 2005. PMID: 15988607

10

The clinical spectrum of fetal Niemann-Pick type C.

Spiegel R, Raas-Rothschild A, Reish O, Regev M, Meiner V, Bargal R, Sury V, Meir K, Nadjari M, Hermann G, Iancu TC, Shalev SA, Zeigler M. Spiegel R, et al. Among authors: reish o. Am J Med Genet A. 2009 Mar;149A(3):446-50. doi: 10.1002/ajmg.a.32642. Am J Med Genet A. 2009. PMID: 19206179

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