Goldman B - Search Results

1

No founder effect detected in Jewish Ashkenazi patients with fragile-X syndrome.

Pesso R, Barkai G, Ravia Y, Gak E, Frydman M, Goldman B, Friedman E. Pesso R, et al. Among authors: goldman b. Hum Genet. 1997 Dec;101(2):186-9. doi: 10.1007/s004390050611. Hum Genet. 1997. PMID: 9402966

2

X-linked recessive primary retinal dysplasia is linked to the Norrie disease locus.

Ravia Y, Braier-Goldstein O, Bat-Miriam KM, Erlich S, Barkai G, Goldman B. Ravia Y, et al. Among authors: goldman b. Hum Mol Genet. 1993 Aug;2(8):1295-7. doi: 10.1093/hmg/2.8.1295. Hum Mol Genet. 1993. PMID: 8401512

3

A missense mutation in ColA1 in Jewish Israeli patient with mild osteogenesis imperfecta, detected by DGGE.

Gat-Yablonski G, Ries L, Lev D, Goldman B, Friedman E. Gat-Yablonski G, et al. Among authors: goldman b. Hum Genet. 1997 Nov;101(1):22-5. doi: 10.1007/s004390050579. Hum Genet. 1997. PMID: 9385363

4

Germline mutational analysis of presenilin 1 and APP genes in Jewish-Israeli individuals with familial or early-onset Alzheimer disease using denaturing gradient gel electrophoresis (DGGE).

Reznik-Wolf H, Treves TA, Shabtai H, Aharon-Peretz J, Chapman J, Davidson M, Barkai G, Hyslop PH, Goldman B, Korczyn AD, Friedman E. Reznik-Wolf H, et al. Among authors: goldman b. Eur J Hum Genet. 1998 Mar-Apr;6(2):176-80. doi: 10.1038/sj.ejhg.5200160. Eur J Hum Genet. 1998. PMID: 9781063

5

CAG repeat polymorphism within the KCNN3 gene is a significant contributor to susceptibility to anorexia nervosa: a case-control study of female patients and several ethnic groups in the Israeli Jewish population.

Koronyo-Hamaoui M, Gak E, Stein D, Frisch A, Danziger Y, Leor S, Michaelovsky E, Laufer N, Carel C, Fennig S, Mimouni M, Apter A, Goldman B, Barkai G, Weizman A. Koronyo-Hamaoui M, et al. Among authors: goldman b. Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):76-80. doi: 10.1002/ajmg.b.20154. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15389773

6

Lower frequency of Gaucher disease carriers among Tay-Sachs disease carriers.

Peleg L, Frisch A, Goldman B, Karpaty M, Narinsky R, Bronstein S, Frydman M. Peleg L, et al. Among authors: goldman b. Eur J Hum Genet. 1998 Mar-Apr;6(2):185-6. doi: 10.1038/sj.ejhg.5200176. Eur J Hum Genet. 1998. PMID: 9781065

7

Mutational analyses of BRCA1 and BRCA2 in Ashkenazi and non-Ashkenazi Jewish women with familial breast and ovarian cancer.

Shiri-Sverdlov R, Oefner P, Green L, Baruch RG, Wagner T, Kruglikova A, Haitchick S, Hofstra RM, Papa MZ, Mulder I, Rizel S, Bar Sade RB, Dagan E, Abdeen Z, Goldman B, Friedman E. Shiri-Sverdlov R, et al. Among authors: goldman b. Hum Mutat. 2000 Dec;16(6):491-501. doi: 10.1002/1098-1004(200012)16:6<491::AID-HUMU6>3.0.CO;2-J. Hum Mutat. 2000. PMID: 11102978

8

Comparative genomic hybridization analysis of radiation-associated and sporadic meningiomas.

Rienstein S, Loven D, Israeli O, Ram Z, Rappaport ZH, Barkai G, Goldman B, Aviram-Goldring A, Friedman E. Rienstein S, et al. Among authors: goldman b. Cancer Genet Cytogenet. 2001 Dec;131(2):135-40. doi: 10.1016/s0165-4608(01)00506-4. Cancer Genet Cytogenet. 2001. PMID: 11750053

9

Association between anorexia nervosa and the hsKCa3 gene: a family-based and case control study.

Koronyo-Hamaoui M, Danziger Y, Frisch A, Stein D, Leor S, Laufer N, Carel C, Fennig S, Minoumi M, Apter A, Goldman B, Barkai G, Weizman A, Gak E. Koronyo-Hamaoui M, et al. Among authors: goldman b. Mol Psychiatry. 2002;7(1):82-5. doi: 10.1038/sj.mp.4000931. Mol Psychiatry. 2002. PMID: 11803450

10

Genotyping of Israeli infertile men with idiopathic oligozoospermia.

Madgar I, Green L, Kent-First M, Weissenberg R, Gershoni-Baruch R, Goldman B, Friedman E. Madgar I, et al. Among authors: goldman b. Clin Genet. 2002 Sep;62(3):203-7. doi: 10.1034/j.1399-0004.2002.620303.x. Clin Genet. 2002. PMID: 12220434

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