FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Ephrat Levy-Lahad

Research Profile

Living Beings

Physiology

Procedures

Concepts & Ideas

Chemicals & Drugs

Geographic Areas

Israel

Disorders

Genes & Molecular Sequences

BRCA1 Genes

Co-author Network

Publications

TOP 3
David A Zeevi; Baruch Brooks; Talia Eldar-Geva; Ephrat Levy-Lahad; Ehud J Margalioth; Arieh Raziel; Paul Renbaum; Raphael Ron-El; Dvorah Strassburger; Gheona Altarescu
Preimplantation genetic diagnosis in genomic regions with duplications and pseudogenes: long-range PCR in the single-cell assay.
Sarah B Pierce; Tom Walsh; Daniel Malach; Rachel Michaelson-Cohen; Ksenija Gersak; Mary-Claire King; Rachel E Klevit; Ming K Lee; Ephrat Levy-Lahad
Mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome.
Eric Duplan; Clément A Gautier; Thomas Goiran; Nathalie Leroudier; Ephrat Levy-Lahad; Paul Renbaum; Jean Sevalle; Julien Viotti; Charlotte Bauer; Frédéric Checler; Olga Corti; Cristine Alves da Costa
Parkin differently regulates presenilin-1 and presenilin-2 functions by direct control of their promoter transcription.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Ephrat Levy-Lahad (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: David A Zeevi; Baruch Brooks; Talia Eldar-Geva; Ephrat Levy-Lahad; Ehud J Margalioth; Arieh Raziel; Paul Renbaum; Raphael Ron-El; Dvorah Strassburger; Gheona Altarescu
Preimplantation genetic diagnosis in genomic regions with duplications and pseudogenes: long-range PCR in the single-cell assay.
Human mutation 2013;34(5):792-9.
2013: Sarah B Pierce; Tom Walsh; Daniel Malach; Rachel Michaelson-Cohen; Ksenija Gersak; Mary-Claire King; Rachel E Klevit; Ming K Lee; Ephrat Levy-Lahad
Mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome.
American journal of human genetics 2013;92(4):614-20.
2013: Eric Duplan; Clément A Gautier; Thomas Goiran; Nathalie Leroudier; Ephrat Levy-Lahad; Paul Renbaum; Jean Sevalle; Julien Viotti; Charlotte Bauer; Frédéric Checler; Olga Corti; Cristine Alves da Costa
Parkin differently regulates presenilin-1 and presenilin-2 functions by direct control of their promoter transcription.
Journal of molecular cell biology 2013;5(2):132-42.
2012: Gheona Altarescu; Rachel Beeri; Talia Eldar-Geva; Ephrat Levy-Lahad; Ehud J Margalioth; Irit Varshaver; Paul Renbaum
PGD for germline mosaicism.
Reproductive biomedicine online 2012;25(4):390-5.
2012: Oded Breuer; Hila Fridman; Ephrat Levy-Lahad; Paul Renbaum; Maha Abdulhadi-Atwan; Sharon Zeligson; David H Zangen
A novel severe N-terminal splice site KISS1R gene mutation causes hypogonadotropic hypogonadism but enables a normal development of neonatal external genitalia.
European journal of endocrinology / European Federation of Endocrine Societies 2012;167(2):209-16.
2012: Shiri Shkedi-Rafid; Efrat Gabai-Kapara; Julia Grinshpun-Cohen; Ephrat Levy-Lahad
BRCA genetic testing of individuals from families with low prevalence of cancer: experiences of carriers and implications for population screening.
Genetics in medicine : official journal of the American College of Medical Genetics 2012;14(7):688-94.
2012: Dalit Ben-Yosef; Gheona Altarescu; Ami Amit; Foad Azem; Rachel Beeri; Ahmi Ben-Yehudah; Ido Eldar; Talia Eldar-Geva; Silvina Epsztejn-Litman; Tsvia Frumkin; Ephrat Levy-Lahad; Mira Malcov; Nava Mey-Raz; Paul Renbaum; Irit Varshaver; Rachel Eiges
Female sex bias in human embryonic stem cell lines.
Stem cells and development 2012;21(3):363-72.
2012: Gheona Altarescu; Lilach Bonstein; T Eldar Geva; Sorina Grisaru-Granovsky; Ephrat Levy-Lahad; Ehud J Margalioth; Hagit Miskin; Irit Varshver; T Eldar-Geva; Paul Renbaum
Preimplantation genetic diagnosis for fetal neonatal alloimmune thrombocytopenia due to antihuman platelet antigen maternal antibodies.
Obstetrics and gynecology 2012;119(2 Pt 1):338-43.
2012: Gheona Altarescu; Rachel Beeri; Rachel Eiges; Talia Eldar-Geva; Deborah Elstein; Silvina Epsztejn-Litman; Ephrat Levy-Lahad; Ehud J Margalioth; Ari Zimran; Paul Renbaum
Prevention of lysosomal storage diseases and derivation of mutant stem cell lines by preimplantation genetic diagnosis.
Molecular biology international 2012;2012():797342.
2011: Marta Sanz-García; Marta Vázquez-Cedeira; Efrat Kellerman; Ephrat Levy-Lahad; Paul Renbaum; Pedro A Lazo
Substrate profiling of human vaccinia-related kinases identifies coilin, a Cajal body nuclear protein, as a phosphorylation target with neurological implications.
Journal of proteomics 2011;75(2):548-60.
2011: Sarah B Pierce; Cailyn H Spurrell; Sunday M Stray; Sharon Zeligson; Michael S Bereman; Siv Fokstuen; Mary-Claire King; Ming K Lee; Ephrat Levy-Lahad; Michael J MacCoss; Jessica B Mandell; Arno G Motulsky
Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria.
Proceedings of the National Academy of Sciences of the United States of America 2011;108(45):18313-7.
2011: Ziva Ben-Neriah; Orly Elpeleg; Michal Inbar-Feigenberg; Rachel Michaelson-Cohen; Michael Nadjari; Avraham Shaag; Sharon Zeligson; Shamir Zenvirt; Ephrat Levy-Lahad
A deleterious founder mutation in the BMPER gene causes diaphanospondylodysostosis (DSD).
American journal of medical genetics. Part A 2011;155A(11):2801-6.
2011: David Zangen; Sharon Zeligson; Shira Perlberg; Paul Renbaum; Maha Abdulhadi-Atwan; Abdulsalam Abu Libdeh; Liran Carmel; Hila Fridman; Ayal Gussow; Moein Kanaan; Yotam Kaufman; Irit Kisslov; Ephrat Levy-Lahad
XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcription.
American journal of human genetics 2011;89(4):572-9.
2011: Sari Lieberman; Shachar Zuckerman; Ephrat Levy-Lahad; Gheona Altarescu
Conflicts regarding genetic counseling for fragile X syndrome screening: a survey of clinical geneticists and genetic counselors in Israel.
American journal of medical genetics. Part A 2011;155A(9):2154-60.
2011: Orit Reish; Céline Huber; Gheona Altarescu; Daphne Chapman-Shimshoni; Ephrat Levy-Lahad; Paul Renbaum; Maya Mashevich; Arnold Munnich; Valérie Cormier-Daire
A non-pathogenic pseudoautosomal region 1 (PAR1) copy number variant downstream of SHOX.
American journal of medical genetics. Part A 2011;155A(4):938-9.
2011: Gheona Altarescu; Orit Reish; Paul Renbaum; Ester Kasterstein; Dvorah Komarovsky; Alisa Komsky; Orna Bern; Dvorah Strassburger; Ephrat Levy-Lahad; Raphael Ron-El
Preimplantation genetic diagnosis (PGD) for SHOX-related haploinsufficiency in conjunction with trisomy 21 detection by molecular analysis.
Journal of assisted reproduction and genetics 2011;28(3):233-8.
2011: Gheona Altarescu; Paul Renbaum; Talia Eldar-Geva; Irit Varshower; Baruch Brooks; Rachel Beeri; Ehud J Margalioth; Ephrat Levy-Lahad; Deborah Elstein; Ari Zimran
Preimplantation genetic diagnosis (PGD) for a treatable disorder: Gaucher disease type 1 as a model.
Blood cells, molecules & diseases 2011;46(1):15-8.
2011: Gheona Altarescu; Orit Barenholz; Rachel Beeri; Baruch Brooks; Ephrat Levy-Lahad; Ehud J Margalioth; Paul Renbaum; Irit Varshaver; Talia Eldar-Geva
Preimplantation genetic diagnosis (PGD)--prevention of the birth of children affected with endocrine diseases.
Journal of pediatric endocrinology & metabolism : JPEM 2011;24(7-8):543-8.
2011: Zippora Brownstein; Bella Davidov; Lilach Friedman; Moshe Frydman; Moien Kanaan; Mary-Claire King; Nitzan Kol; Ming K Lee; Dorit Lev; Ephrat Levy-Lahad; Sari Lieberman; Varda Oron-Karni; Thomas Parzefall; Michele Rahile; Hashem Shahin; Stavit Shalev; Mordechai Shohat; Noam Shomron; Tom Walsh; Amal Abu Rayyan; Karen B Avraham
Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families.
Genome biology 2011;12(9):R89.
2010: Avi Tsafrir; Gheona Altarescu; Ehud J Margalioth; Baruch Brooks; Paul Renbaum; Ephrat Levy-Lahad; Ron Rabinowitz; Irit Varshaver; Talia Eldar-Geva
PGD for fragile X syndrome: ovarian function is the main determinant of success.
Human reproduction (Oxford, England) 2010;25(10):2629-36.
2010: Orit Reish; Céline Huber; Gheona Altarescu; Daphne Chapman-Shimshoni; Ephrat Levy-Lahad; Paul Renbaum; Maya Mashevich; Arnold Munnich; Valérie Cormier-Daire
Mosaic compound heterozygosity of SHOX resulting in Leri-Weill dyschondrosteosis with marked short stature: implications for disease mechanisms and recurrence risks.
American journal of medical genetics. Part A 2010;152A(9):2230-5.
2010: Sarah B Pierce; Tom Walsh; Karen M Chisholm; Ming K Lee; Anne M Thornton; Agata Fiumara; John M Opitz; Ephrat Levy-Lahad; Rachel E Klevit; Mary-Claire King
Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome.
American journal of human genetics 2010;87(2):282-8.
2010: Tayfun Ozçelik; Moien Kanaan; Karen B Avraham; Drakoulis Yannoukakos; André Mégarbané; Ghazi O Tadmouri; Lefkos Middleton; Giovanni Romeo; Mary-Claire King; Ephrat Levy-Lahad
Collaborative genomics for human health and cooperation in the Mediterranean region.
Nature genetics 2010;42(8):641-5.
2010: Ephrat Levy-Lahad
Fanconi anemia and breast cancer susceptibility meet again.
Nature genetics 2010;42(5):368-9.
2010: Orit Reish; Niva Shefer-Kaufmann; Daphne Chapman Shimshoni; Paul Renbaum; Avi Orr-Urtreger; Hillel Steiner; Micha Rapoport; Ephrat Levy-Lahad; Gheona Altarescu
Frequencies of C282Y and H63D alleles in the HFE gene among various Jewish ethnic groups in Israel: a change of concept required.
Genetics in medicine : official journal of the American College of Medical Genetics 2010;12(2):122-5.
2009: Gheona Altarescu; Talia Eldar-Geva; Irit Varshower; Barry Brooks; Edith Zylber Haran; Ehud J Margalioth; Ephrat Levy-Lahad; Paul Renbaum
Real-time reverse linkage using polar body analysis for preimplantation genetic diagnosis in female carriers of de novo mutations.
Human reproduction (Oxford, England) 2009;24(12):3225-9.
2009: Ying Li; Gheona Altarescu; Paul Renbaum; Talia Eldar-Geva; Ephrat Levy-Lahad; Ehud J Margalioth; Xiaoyan Zhong; Sinuhe Hahn; Wolfgang Holzgreve
Non-invasive prenatal diagnosis using cell-free fetal DNA in maternal plasma from PGD pregnancies.
Reproductive biomedicine online 2009;19(5):714-20.
2009: Julie Dunys; Jean Sevalle; Emilie Giaime; Raphaëlle Pardossi-Piquard; Michael P Vitek; Paul Renbaum; Ephrat Levy-Lahad; Yun-Wu Zhang; Huaxi Xu; Frédéric Checler; Cristine Alves da Costa
p53-dependent control of transactivation of the Pen2 promoter by presenilins.
Journal of cell science 2009;122(Pt 21):4003-8.
2009: Reeval Segel; Ephrat Levy-Lahad; Francesca Pasutto; Elie Picard; Anita Rauch; Gheona Alterescu; Michael S Schimmel
Pulmonary hypoplasia-diaphragmatic hernia-anophthalmia-cardiac defect (PDAC) syndrome due to STRA6 mutations--what are the minimal criteria?
American journal of medical genetics. Part A 2009;149A(11):2457-63.
2009: Hadile Ounallah-Saad; Rachel Beeri; Inbal Goshen; Raz Yirmiya; Paul Renbaum; Ephrat Levy-Lahad
Transcriptional regulation of the murine Presenilin-2 gene reveals similarities and differences to its human orthologue.
Gene 2009;446(2):81-9.
2009: Ephrat Levy-Lahad
Population-based BRCA1/BRCA2 screening in Ashkenazi Jews: a call for evidence.
Genetics in medicine : official journal of the American College of Medical Genetics 2009;11(9):620-1.
2009: Paul Renbaum; Efrat Kellerman; Ranit Jaron; Dan Geiger; Reeval Segel; Ming Lee; Mary-Claire King; Ephrat Levy-Lahad
Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 gene.
American journal of human genetics 2009;85(2):281-9.
2009: Gheona Altarescu; Talia Eldar-Geva; Baruch Brooks; Edith Zylber-Haran; Irit Varshaver; Ehud J Margalioth; Ephrat Levy-Lahad; Paul Renbaum
Preimplantation genetic diagnosis (PGD) for nonsyndromic deafness by polar body and blastomere biopsy.
Journal of assisted reproduction and genetics 2009;26(7):391-7.
2008: S Zuckerman; Amnon Lahad; Ari Zimran; Ephrat Levy-Lahad; Michal Sagi
Attitudes of couples identified through screening as carriers of Gaucher disease type 1.
Clinical genetics 2008;74(6):566-70.
2008: Gheona Altarescu; Talia Eldar-Geva; Barry Brooks; Ehud Margalioth; Ephrat Levy-Lahad; Paul Renbaum
PGD on a recombinant allele: crossover between the TSC2 gene and 'linked' markers impairs accurate diagnosis.
Prenatal diagnosis 2008;28(10):929-33.
2008: Ephrat Levy-Lahad; Shachar Zuckerman; Michal Sagi
Response to ACMG guideline: carrier screening in individuals of Ashkenazi Jewish decent.
Genetics in medicine : official journal of the American College of Medical Genetics 2008;10(6):462; author reply 463.
2008: Gheona Altarescu; Paul Renbaum; B Brooks P; Ehud J Margalioth; Avraham Ben-Chetrit; G Munter; Ephrat Levy-Lahad; Talia Eldar-Geva
Successful polar body-based preimplantation genetic diagnosis for achondroplasia.
Reproductive biomedicine online 2008;16(2):276-82.
2008: Michael Kaplan; Tina Slusher; Paul Renbaum; Dominic F Essiet; Sunday Pam; Ephrat Levy-Lahad; Cathy Hammerman
(TA)n UDP-glucuronosyltransferase 1A1 promoter polymorphism in Nigerian neonates.
Pediatric research 2008;63(1):109-11.
2007: Inbal Weiss-Salz; Susan Harlap; Yechiel Friedlander; Luna Kaduri; Ephrat Levy-Lahad; Rivka Yanetz; Lisa Deutsch; Hagit Hochner; Ora Paltiel
Ethnic ancestry and increased paternal age are risk factors for breast cancer before the age of 40 years.
European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 2007;16(6):549-54.
2007: Shachar Zuckerman; Amnon Lahad; Amir Shmueli; Ari Zimran; Leah Peleg; Avi Orr-Urtreger; Ephrat Levy-Lahad; Michal Sagi
Carrier screening for Gaucher disease: lessons for low-penetrance, treatable diseases.
JAMA : the journal of the American Medical Association 2007;298(11):1281-90.
2007: Inbal Goshen; Tirzah Kreisel; Hadile Ounallah-Saad; Paul Renbaum; Yael Zalzstein; Tamir Ben-Hur; Ephrat Levy-Lahad; Raz Yirmiya
A dual role for interleukin-1 in hippocampal-dependent memory processes.
Psychoneuroendocrinology 2007;32(8-10):1106-15.
2007: Gheona Altarescu; Baruch Brooks; Ehud J Margalioth; Talia Eldar-Geva; Ephrat Levy-Lahad; Paul Renbaum
Simultaneous preimplantation genetic diagnosis for Tay-Sachs and Gaucher disease.
Reproductive biomedicine online 2007;15(1):83-8.
2007: Michael Kaplan; Paul Renbaum; Hendrik J Vreman; Ronald J Wong; Ephrat Levy-Lahad; Cathy Hammerman; David K Stevenson
(TA)n UGT 1A1 promoter polymorphism: a crucial factor in the pathophysiology of jaundice in G-6-PD deficient neonates.
Pediatric research 2007;61(6):727-31.
2007: Paul Renbaum; Baruch Brooks; Y Kaplan; Talia Eldar-Geva; Ehud J Margalioth; Ephrat Levy-Lahad; Gheona Altarescu
Advantages of multiple markers and polar body analysis in preimplantation genetic diagnosis for Alagille disease.
Prenatal diagnosis 2007;27(4):317-21.
2007: Ephrat Levy-Lahad; Eitan Friedman
Cancer risks among BRCA1 and BRCA2 mutation carriers.
British journal of cancer 2007;96(1):11-5.
2006: Gheona Altarescu; Baruch Brooks; Y Kaplan; Talia Eldar-Geva; Ehud J Margalioth; Ephrat Levy-Lahad; Paul Renbaum
Single-sperm analysis for haplotype construction of de-novo paternal mutations: application to PGD for neurofibromatosis type 1.
Human reproduction (Oxford, England) 2006;21(8):2047-51.
2006: Sharon Simchoni; Eitan Friedman; Bella Kaufman; Ruth Gershoni-Baruch; Avi Orr-Urtreger; Inbal Kedar-Barnes; Ronit Shiri-Sverdlov; Efrat Dagan; Sigal Tsabari; Mordechai Shohat; Raphael Catane; Mary-Claire King; Amnon Lahad; Ephrat Levy-Lahad
Familial clustering of site-specific cancer risks associated with BRCA1 and BRCA2 mutations in the Ashkenazi Jewish population.
Proceedings of the National Academy of Sciences of the United States of America 2006;103(10):3770-4.
2005: Valérie Delague; Eliane Chouery; Sandra Corbani; Ismat Ghanem; Suhail Aamar; Judith Fischer; Ephrat Levy-Lahad; J Andoni Urtizberea; André Mégarbané
Molecular study of WISP3 in nine families originating from the Middle-East and presenting with progressive pseudorheumatoid dysplasia: identification of two novel mutations, and description of a founder effect.
American journal of medical genetics. Part A 2005;138A(2):118-26.
2005: Avraham Shaag; Tom Walsh; Paul Renbaum; Tomas Kirchhoff; Khedoudja Nafa; Stacey Shiovitz; Jessica B Mandell; Piri Welcsh; Ming K Lee; Nathan Ellis; Kenneth Offit; Ephrat Levy-Lahad; Mary-Claire King
Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population.
Human molecular genetics 2005;14(4):555-63.
2003: Paul Renbaum; Rachel Beeri; Efrat Gabai; Merav Amiel; Moran Gal; Markus U Ehrengruber; Ephrat Levy-Lahad
Egr-1 upregulates the Alzheimer's disease presenilin-2 gene in neuronal cells.
Gene 2003;318():113-24.
2003: Ephrat Levy-Lahad; Sharon E Plon
Cancer. A risky business--assessing breast cancer risk.
Science (New York, N.Y.) 2003;302(5645):574-5.
2003: Emanuel Yakobson; Shlomit Eisenberg; Ruth Isacson; David Halle; Ephrat Levy-Lahad; Raphael Catane; Mark Safro; Vladimir Sobolev; Thomas Huot; Gordon Peters; Anna Ruiz; Josep Malvehy; Suzana Puig; Agnès Chompret; Marie-Fracoise Avril; Raphael Shafir; Hava Peretz; Brigitte Bressac De-Paillerets
A single Mediterranean, possibly Jewish, origin for the Val59Gly CDKN2A mutation in four melanoma-prone families.
European journal of human genetics : EJHG 2003;11(4):288-96.
2002: Michael Kaplan; Cathy Hammerman; Firmino Francesco Rubaltelli; Maria Teresa Vilei; Ephrat Levy-Lahad; Paul Renbaum; Hendrik J Vreman; David K Stevenson; Maurizio Muraca
Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism.
Hepatology (Baltimore, Md.) 2002;35(4):905-11.
2002: L I Idelson; I I Albert; B Rudensky; Ephrat Levy-Lahad; Paul Renbaum; G Klein
[Combination of heterozygote blood coagulation factor V Leiden carriage with erythrocytosis as a cause of the hip deep vein thrombosis].
Terapevticheskiĭ arkhiv 2002;74(2):66-70.
2001: M Kaplan; Ephrat Levy-Lahad; Cathy Hammerman; Paul Renbaum; J Halevy
Sex distribution in Gilbert's syndrome.
The Israel Medical Association journal : IMAJ 2001;3(12):989.
2001: Michael Kaplan; Cathy Hammerman; Paul Renbaum; Ephrat Levy-Lahad; Hendrik J Vreman; David K Stevenson
Differing pathogenesis of perinatal bilirubinemia in glucose-6-phosphate dehydrogenase-deficient versus-normal neonates.
Pediatric research 2001;50(4):532-7.
2001: Linda E Pinsky; J B Culver; J Hull; Ephrat Levy-Lahad; M Daly; Wylie Burke
Why should primary care physicians know about breast cancer genetics?
The Western journal of medicine 2001;175(3):168-73.
2001: Ephrat Levy-Lahad; Amnon Lahad; Shlomit Eisenberg; Efrat Dagan; Tamar Paperna; Lior Kasinetz; Raphael Catane; Bella Kaufman; Uziel Beller; Paul Renbaum; Ruth Gershoni-Baruch
A single nucleotide polymorphism in the RAD51 gene modifies cancer risk in BRCA2 but not BRCA1 carriers.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(6):3232-6.
2000: Deborah Elstein; Paul Renbaum; Ephrat Levy-Lahad; Ari Zimran
Incidence of thrombophilia in patients with Gaucher disease.
American journal of medical genetics 2000;95(5):429-31.
2000: M Kaplan; Cathy Hammerman; Paul Renbaum; G Klein; Ephrat Levy-Lahad
Gilbert's syndrome and hyperbilirubinaemia in ABO-incompatible neonates.
Lancet 2000;356(9230):652-3.
2000: Ofer Lavie; Gila Hornreich; Alon Ben-Arie; Paul Renbaum; Ephrat Levy-Lahad; Uziel Beller
BRCA1 germline mutations in women with uterine serous papillary carcinoma.
Obstetrics and gynecology 2000;96(1):28-32.
2000: Ephrat Levy-Lahad; M Krieger; O Gottfeld; Paul Renbaum; G Klein; Shlomit Eisenberg; Amnon Lahad; Bella Kaufman; Raphael Catane
BRCA1 and BRCA2 mutation carriers as potential candidates for chemoprevention trials.
Journal of cellular biochemistry. Supplement 2000;34():13-8.
1999: E Rosen; Paul Renbaum; J Heyd; Ephrat Levy-Lahad
High frequency of factor V Leiden in a population of Israeli Arabs.
Thrombosis and haemostasis 1999;82(6):1768.
1999: Gila Hornreich; Uziel Beller; Ofer Lavie; Paul Renbaum; Y Cohen; Ephrat Levy-Lahad
Is uterine serous papillary carcinoma a BRCA1-related disease? Case report and review of the literature.
Gynecologic oncology 1999;75(2):300-4.
1999: Michael Kaplan; E Beutler; Hendrik J Vreman; Cathy Hammerman; Ephrat Levy-Lahad; Paul Renbaum; David K Stevenson
Neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient heterozygotes.
Pediatrics 1999;104(1 Pt 1):68-74.
1998: Eitan Friedman; R Bar-Sade Bruchim; A Kruglikova; S Risel; Ephrat Levy-Lahad; David Halle; E Bar-On; Ruth Gershoni-Baruch; Efrat Dagan; I Kepten; Tamar Peretz; Israela Lerer; N Wienberg; A Shushan; A D Abeliovich
Double heterozygotes for the Ashkenazi founder mutations in BRCA1 and BRCA2 genes.
American journal of human genetics 1998;63(4):1224-7.
1998: Paul Renbaum; Ephrat Levy-Lahad
Monogenic determinants of familial Alzheimer's disease: presenilin-2 mutations.
Cellular and molecular life sciences : CMLS 1998;54(9):910-9.
1998: Ephrat Levy-Lahad; D Tsuang; Thomas D Bird
Recent advances in the genetics of Alzheimer's disease.
Journal of geriatric psychiatry and neurology 1998;11(2):42-54.
1998: Mia Horowitz; Metsada Pasmanik-Chor; Zvi Borochowitz; Tzipora C Falik-Zaccai; K Heldmann; Rivka Carmi; Ruti Parvari; H Beit-Or; Boleslaw Goldman; Leah Peleg; Ephrat Levy-Lahad; Paul Renbaum; S Legum; Ruth Shomrat; H Yeger; D Benbenisti; Ruth Navon; Vardit Dror; Mordechai Shohat; Nurit Magal; N Navot; N Eyal
Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewish population.
Human mutation 1998;12(4):240-4.
1997: Uziel Beller; David Halle; Raphael Catane; Bella Kaufman; Gila Hornreich; Ephrat Levy-Lahad
High frequency of BRCA1 and BRCA2 germline mutations in Ashkenazi Jewish ovarian cancer patients, regardless of family history.
Gynecologic oncology 1997;67(2):123-6.
1997: Michael Kaplan; Paul Renbaum; Ephrat Levy-Lahad; Cathy Hammerman; Amnon Lahad; E Beutler
Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(22):12128-32.
1997: Ephrat Levy-Lahad; Raphael Catane; Shlomit Eisenberg; Bella Kaufman; Gila Hornreich; E Lishinsky; M Shohat; B L Weber; Uziel Beller; Amnon Lahad; David Halle
Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families.
American journal of human genetics 1997;60(5):1059-67.
1996: Thomas D Bird; Ephrat Levy-Lahad; Parvoneh Poorkaj-Navas; V Sharma; EJ Nemens; Amnon Lahad; T H Lampe; Gerard D Schellenberg
Wide range in age of onset for chromosome 1--related familial Alzheimer's disease.
Annals of neurology 1996;40(6):932-6.
1996: Ephrat Levy-Lahad; Thomas D Bird
Genetic factors in Alzheimer's disease: a review of recent advances.
Annals of neurology 1996;40(6):829-40.
1996: Greer M Murphy; Lysia S Forno; William G Ellis; David Nochlin; Ephrat Levy-Lahad; Parvoneh Poorkaj-Navas; Thomas D Bird; Z Jiang; Barbara Cordell
Antibodies to presenilin proteins detect neurofibrillary tangles in Alzheimer's disease.
The American journal of pathology 1996;149(6):1839-46.
1996: Donalyn Scheuner; Christopher B Eckman; M Jensen; X Song; Martin Citron; N Suzuki; Thomas D Bird; John Hardy; Michael Hutton; Walter A Kukull; Eric B Larson; Ephrat Levy-Lahad; Matti Viitanen; Elaine Peskind; Parvoneh Poorkaj-Navas; Gerard D Schellenberg; Rudolph E Tanzi; Wilma Wasco; Lars Lannfelt; Dennis J Selkoe; Steven G Younkin
Secreted amyloid beta-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease.
Nature medicine 1996;2(8):864-70.
1996: Ephrat Levy-Lahad; Parvoneh Poorkaj-Navas; K Wang; Y H Fu; Oshima Junko; J Mulligan; Gerard D Schellenberg
Genomic structure and expression of STM2, the chromosome 1 familial Alzheimer disease gene.
Genomics 1996;34(2):198-204.
1995: Ephrat Levy-Lahad; Amnon Lahad; Ellen M Wijsman; Thomas D Bird; Gerard D Schellenberg
Apolipoprotein E genotypes and age of onset in early-onset familial Alzheimer's disease.
Annals of neurology 1995;38(4):678-80.
1995: Ephrat Levy-Lahad; Wilma Wasco; Parvoneh Poorkaj-Navas; Donna M Romano; Oshima Junko; Warren H Pettingell; Chang-En Yu; P D Jondro; S D Schmidt; K Wang
Candidate gene for the chromosome 1 familial Alzheimer's disease locus.
Science (New York, N.Y.) 1995;269(5226):973-7.
1995: Ephrat Levy-Lahad; Ellen M Wijsman; EJ Nemens; L Anderson; Katrina Goddard; J L Weber; Thomas D Bird; Gerard D Schellenberg
A familial Alzheimer's disease locus on chromosome 1.
Science (New York, N.Y.) 1995;269(5226):970-3.
1994: Amnon Lahad; Ephrat Levy-Lahad
Nurse practitioners as endoscopists.
The New England journal of medicine 1994;330(21):1534; author reply 1535.