Ephrat Levy-Lahad
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Explore the profile of Ephrat Levy-Lahad including associated specialties, affiliations and a list of published articles.
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123
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2547
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Recent Articles
1.
Cohen A, Rossetti R, Florsheim N, Samson A, Renbaum P, Carbone E, et al.
J Endocr Soc
. 2025 Jan;
9(2):bvae221.
PMID: 39850788
Context: Despite a growing number of studies, the genetic etiology in many cases of ovarian dysgenesis is incompletely understood. Objectives: This work aimed to study the genetic etiology causing absence...
2.
Lolas-Hamameh S, Lieberman S, Sarahneh A, Walsh T, Lee M, Gulsuner S, et al.
J Natl Cancer Inst
. 2024 Dec;
PMID: 39673796
Pathogenic TP53 germline variants cause young-onset breast cancer and other cancers of the Li-Fraumeni syndrome (LFS) spectrum, but the clinical consequences of partial-loss-of function TP53 variants are incompletely understood. In...
3.
Passi G, Lieberman S, Zahdeh F, Murik O, Renbaum P, Beeri R, et al.
Brief Bioinform
. 2024 Jul;
25(4).
PMID: 39038933
Breast cancer (BC) is the most common malignancy affecting Western women today. It is estimated that as many as 10% of BC cases can be attributed to germline variants. However,...
4.
Canavati C, Sherill-Rofe D, Kamal L, Bloch I, Zahdeh F, Sharon E, et al.
Genome Med
. 2024 Jan;
16(1):4.
PMID: 38178268
Background: Next-generation sequencing (NGS) has significantly transformed the landscape of identifying disease-causing genes associated with genetic disorders. However, a substantial portion of sequenced patients remains undiagnosed. This may be attributed...
5.
Florsheim N, Naugolni L, Zahdeh F, Lobel O, Terespolsky B, Michaelson-Cohen R, et al.
Eur J Endocrinol
. 2023 Sep;
189(3):K7-K14.
PMID: 37740949
Ovarian dysgenesis (OD), an XX disorder of sex development, presents with primary amenorrhea, hypergonadotrophic hypogonadism, and infertility. In an Ashkenazi Jewish patient with OD, whole exome sequencing identified compound heterozygous...
6.
Michaelson-Cohen R, Laitman Y, Kedar I, Baris-Feldman H, Reish O, Lieberman S, et al.
Harefuah
. 2023 Jul;
162(6):370-375.
PMID: 37394440
Introduction: Hereditary breast and ovarian cancer (HBOC) is predominantly accounted for by pathogenic variants (PVs) in BRCA1/BRCA2 genes. Population screening for recurring PVs in Ashkenazi Jews (AJ) was incorporated into...
7.
Michaelson-Cohen R, Cohen M, Cohen C, Greenberg D, Shmueli A, Lieberman S, et al.
Cancers (Basel)
. 2022 Dec;
14(24).
PMID: 36551598
Identifying carriers of pathogenic BRCA1/BRCA2 variants reduces cancer morbidity and mortality through surveillance and prevention. We analyzed the cost-effectiveness of BRCA1/BRCA2 population screening (PS) in Ashkenazi Jews (AJ), for whom...
8.
Shaashua L, Ben-Shmuel A, Pevsner-Fischer M, Friedman G, Levi-Galibov O, Nandakumar S, et al.
Nat Commun
. 2022 Nov;
13(1):6513.
PMID: 36316305
Tumors initiate by mutations in cancer cells, and progress through interactions of the cancer cells with non-malignant cells of the tumor microenvironment. Major players in the tumor microenvironment are cancer-associated...
9.
Rabin R, Hirsch Y, Chung W, Ekstein J, Levy-Lahad E, Zuckerman S, et al.
Am J Med Genet A
. 2022 Aug;
188(10):3110-3117.
PMID: 35943032
Bi-allelic variants in COLEC11 and MASP1 have been associated with 3MC syndrome, a clinical entity made of up four rare autosomal recessive disorders: Carnevale, Mingarelli, Malpuech, and Michels syndromes, characterized...
10.
Lieberman S, Goldvaser H, Levy-Lahad E
J Clin Oncol
. 2022 Mar;
40(14):1590-1594.
PMID: 35286153
No abstract available.