Yael Goldberg
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Explore the profile of Yael Goldberg including associated specialties, affiliations and a list of published articles.
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106
Citations
1123
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Recent Articles
1.
Hatch S, Seitz D, Bruneau M, Ewa V, Feldman S, Goldberg Y, et al.
Can Geriatr J
. 2025 Mar;
28(1):91-102.
PMID: 40051590
In Canada, approximately 730,000 people are currently living with dementia. Over 75% will experience behavioural and psychological symptoms of dementia (BPSD). There is a lack of consensus on best practices...
2.
Abu Shtaya A, Nathan S, Kedar I, Friedman E, Half E, Lidzbarsky G, et al.
Fam Cancer
. 2024 Nov;
24(1):6.
PMID: 39546165
Deciphering the spectrum and founder disease-causing variants (DCVs) in specific populations can shape and facilitate the diagnostic process of Lynch Syndrome (LS). The aim of this report was to comprehensively...
3.
Rigaud C, Forster V, Al-Tarrah H, Attarbaschi A, Bianchi V, Burke A, et al.
Pediatr Blood Cancer
. 2024 Sep;
71(12):e31302.
PMID: 39300701
Background: Constitutional mismatch repair deficiency syndrome (CMMRD) is a rare childhood cancer predisposition syndrome associated with a broad spectrum of malignancies, including non-Hodgkin lymphomas (NHL). Most patients die due to...
4.
Brabbing-Goldstein D, Bazak L, Ruhrman-Shahar N, Lidzbarsky G, Orenstein N, Lifshiz-Kalis M, et al.
Prenat Diagn
. 2024 Sep;
44(12):1423-1434.
PMID: 39237446
Objective: To investigate how many novel pathogenic (P) and likely pathogenic (LP) nonprotein-truncating or noncanonical splicing variants would be classified as variants of unknown significance (VUS) if they were detected...
5.
Regev M, Dori A, Altarescu G, Barel O, Basel-Salmon L, Greenbaum L, et al.
Gene
. 2024 Jun;
927:148725.
PMID: 38914246
Mutated skeletal muscle ryanodine receptor-1 (RYR1) gene is associated with a spectrum of autosomal dominant and recessive RyR1-related disorders with a wide phenotype. This report describes a variable phenotype associated...
6.
Torgeman S, Pleban T, Goldberg Y, Ferrante P, Aprea G, Giuliano G, et al.
Plant J
. 2024 Apr;
119(1):595-603.
PMID: 38576107
Wild species are an invaluable source of new traits for crop improvement. Over the years, the tomato community bred cultivated lines that carry introgressions from different species of the tomato...
7.
Yerushalmi R, Pomerantz A, Lewin R, Paluch-Shimon S, Soussan-Gutman L, Baehner F, et al.
Breast Cancer Res Treat
. 2024 Apr;
206(1):67-76.
PMID: 38568368
Purpose: We compared 21-gene recurrence score (RS) distribution and expression of the single-gene/gene groups within this assay between BC patients with pathogenic variants (PV) in BRCA1/2 vs the general 21-gene-tested...
8.
Abu Shtaya A, Kedar I, Bazak L, Basel-Salmon L, Barhom S, Naftali M, et al.
Genes (Basel)
. 2024 Mar;
15(3).
PMID: 38540414
POT1 (Protection of Telomeres 1) is a key component of the six-membered shelterin complex that plays a critical role in telomere protection and length regulation. Germline variants in the gene...
9.
Deitch I, Itskov S, Panneman D, Abu Shtaya A, Saban T, Goldberg Y, et al.
Curr Issues Mol Biol
. 2024 Mar;
46(3):2566-2575.
PMID: 38534779
Bardet-Biedl syndrome (BBS), one of the most common forms of syndromic inherited retinal diseases (IRDs), is characterized by the combination of retinal degeneration with additional extra-ocular manifestations, including obesity, intellectual...
10.
Ben-Zion Berliner M, Yust-Katz S, Lavie I, Goldberg Y, Kedar I, Yerushalmi R
BMC Cancer
. 2024 Feb;
24(1):219.
PMID: 38365640
Background: Breast cancer is a common cause for central nervous system (CNS) metastasis, resulting in a significant reduction in overall survival. Germline pathogenic variants (PVs) in BRCA1/2 are the most...