| Increased fibrosis progression rates in hepatitis C patients carrying the prothrombin G20210A mutation. Maharshak N., Halfon P., Deutsch V., Peretz H., Berliner S., Fishman S., Zelber-Sagi S., Rozovski U., Leshno M., Oren R.
World J. Gastroenterol. 17:5007-5013(2011) · Mapped (8) |
| Association of the -757T>C polymorphism in the CRP gene with circulating C-reactive protein levels and carotid atherosclerosis. Ben Assayag E., Shenhar-Tsarfaty S., Bova I., Berliner S., Usher S., Peretz H., Shapira I., Bornstein N.M.
Thromb. Res. 124:458-462(2009) · Mapped (3) |
| Disulfide bond disruption by a beta 3-Cys549Arg mutation in six Jordanian families with Glanzmann thrombasthenia causes diminished production of constitutively active alpha IIb beta 3. Mor-Cohen R., Rosenberg N., Peretz H., Landau M., Coller B.S., Awidi A., Seligsohn U.
Thromb. Haemost. 98:1257-1265(2007) · Mapped (11) |
| Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the human molybdenum cofactor sulfurase (HMCS) associated with type II classical xanthinuria. Peretz H., Naamati M.S., Levartovsky D., Lagziel A., Shani E., Horn I., Shalev H., Landau D.
Mol. Genet. Metab. 91:23-29(2007) · UniProtKB (1) |
| Triggered C-reactive protein (CRP) concentrations and the CRP gene -717A>G polymorphism in acute stroke or transient ischemic attack. Ben-Assayag E., Shenhar-Tsarfaty S., Bova I., Berliner S., Shopin L., Peretz H., Usher S., Shapira I., Bornstein N.M.
Eur. J. Neurol. 14:315-320(2007) · Mapped (3) |
| Diversity of Glanzmann thrombasthenia in southern India: 10 novel mutations identified among 15 unrelated patients. Nelson E.J., Nair S.C., Peretz H., Coller B.S., Seligsohn U., Chandy M., Srivastava A.
J. Thromb. Haemost. 4:1730-1737(2006) · Mapped (11) |
| Role of CYP2D6 polymorphism in predicting liver fibrosis progression rate in Caucasian patients with chronic hepatitis C. Fishman S., Lurie Y., Peretz H., Morad T., Grynberg E., Blendis L.M., Leshno M., Brazowski E., Rosner G., Halpern Z. et al.
Liver Int. 26:279-284(2006) · Mapped (18) |
| Gender differences in the expression of erythrocyte aggregation in relation to B beta-fibrinogen gene polymorphisms in apparently healthy individuals. Ben Assayag E., Bova I., Berliner S., Peretz H., Usher S., Shapira I., Bornstein N.M.
Thromb. Haemost. 95:428-433(2006) · Mapped (5) |
| Warfarin therapy is feasible in CYP2C9*3 homozygous patients. Ablin J., Cabili S., Eldor A., Lagziel A., Peretz H.
Eur. J. Intern. Med. 15:22-27(2004) · Mapped (7) |
| Major mutations in calf-1 and calf-2 domains of glycoprotein IIb in patients with Glanzmann thrombasthenia enable GPIIb/IIIa complex formation, but impair its transport from the endoplasmic reticulum to the Golgi apparatus. Rosenberg N., Yatuv R., Sobolev V., Peretz H., Zivelin A., Seligsohn U.
Blood 101:4808-4815(2003) · Mapped (11) |
| Apolipoprotein-E genotype and the risk of developing cholelithiasis following bariatric surgery: a clue to prevention of routine prophylactic cholecystectomy. Abu Abeid S., Szold A., Gavert N., Goldiner I., Grynberg E., Peretz H., Konikoff F.M.
Obes Surg 12:354-357(2002) · Mapped (5) |
| Molecular characterization of four novel mutations causing factor VII deficiency. Tamary H., Fromovich-Amit Y., Shalmon L., Zaizov R., Yaniv I., Klar A., Peretz H., Brenner B., Lanir N., Zivelin A. et al.
Hematol. J. 1:382-389(2000) · Mapped (5) |
| Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene. Zivelin A., Bauduer F., Ducout L., Peretz H., Rosenberg N., Yatuv R., Seligsohn U.
Blood 99:2448-2454(2002) · UniProtKB (1) |
| The risk of fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known fragile X families. Geva E., Yaron Y., Shomrat R., Ben-Yehuda A., Zabari S., Peretz H., Naiman T., Yeger H., Orr-Urtreger A.
Genet. Test. 4:289-292(2000) · Mapped (8) |
| XDH gene mutation is the underlying cause of classical xanthinuria: a second report. Levartovsky D., Lagziel A., Sperling O., Liberman U., Yaron M., Hosoya T., Ichida K., Peretz H.
Kidney Int. 57:2215-2220(2000) · UniProtKB (1) |
| The human platelet alphaIIb gene is not closely linked to its integrin partner beta3. Thornton M.A., Poncz M., Korostishevsky M., Yakobson E., Usher S., Seligsohn U., Peretz H.
Blood 94:2039-2047(1999) · UniProtKB (1) |
| Cys 618 Arg mutation in the RET proto-oncogene associated with familial medullary thyroid carcinoma and maternally transmitted Hirschsprung's disease suggesting a role for imprinting. Peretz H., Luboshitsky R., Baron E., Biton A., Gershoni R., Usher S., Grynberg E., Yakobson E., Graff E., Lapidot M.
Hum. Mutat. 10:155-159(1997) · UniProtKB (1) |
| Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb gene. Peretz H., Rosenberg N., Usher S., Graff E., Newman P.J., Coller B.S., Seligsohn U.
Blood 85:414-420(1995) · Mapped (6) |
