Dani Bercovich
Tel Hay, Z 12208, Israel
Last Updated: 09/26/2026
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Found 25 publications
Epitranscriptomic variation in banded newts (Ommatotriton vittatus) across life stages and sexes in the semi-arid habitat in northern Israel.
Journal: Comparative biochemistry and physiology. Part D, Genomics & proteomics
Published: October 20, 2025
A case of Ververi-Brady syndrome due to QRICH1 loss of function and the literature review.
Journal: American journal of medical genetics. Part A
Published: October 20, 2020
High Prevalence of Hearing Impairment in Primary Congenital Hypothyroidism.
Journal: European thyroid journal
Published: April 23, 2020
Extreme Short Stature and Severe Neurological Impairment in a 17-Year-Old Male With Untreated Combined Pituitary Hormone Deficiency Due to POU1F1 Mutation.
Journal: Frontiers in endocrinology
Published: March 28, 2019
POLD1 and POLE Gene Mutations in Jewish Cohorts of Early-Onset Colorectal Cancer and of Multiple Colorectal Adenomas.
Journal: Diseases of the colon and rectum
Published: August 08, 2018
The significance of human spermatozoa vacuoles can be elucidated by a novel procedure of array comparative genomic hybridization.
Journal: Human reproduction (Oxford, England)
Published: November 30, 2017
Mammal domestication and the symbiotic spectrum.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 15, 2017
A novel heterozygous IGF-1 receptor mutation associated with hypoglycemia.
Journal: Endocrine connections
Published: June 08, 2017
Frequency of canine nt230(del4) MDR1 mutation in prone pure breeds, their crosses and mongrels in Israel - insights from a worldwide comparative perspective.
Journal: BMC veterinary research
Published: May 14, 2017
Immunity, Life and Dancing Starlings: A Physician's Perspective.
Journal: The Israel Medical Association journal : IMAJ
Published: May 05, 2017
Severe infantile male encephalopathy is a result of early post-zygotic WDR45 somatic mutation.
Journal: Clinical genetics
Published: July 03, 2016
Familial Central Hypothyroidism Caused by a Novel IGSF1 Gene Mutation.
Journal: Thyroid : official journal of the American Thyroid Association
Published: June 17, 2016
Last Updated: 09/26/2026