Adel Shalata

Haifa, HA 32000, Israel

Last Updated: 09/26/2026

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Found 48 publications

Failure to Fuse Shut Eyelids, a Novel Unique Sign in Affected Fetus with Homozygous PPP1R13L Pathogenic Variant-A Case Report and Review of the Literature.

Failure to Fuse Shut Eyelids, a Novel Unique Sign in Affected Fetus with Homozygous PPP1R13L Pathogenic Variant-A Case Report and Review of the Literature.

Journal: International journal of molecular sciences

Published: May 16, 2026

IL-34 as a Novel Mediator Linking Vitamin D Deficiency with Osteoporosis and Knee Osteoarthritis.

IL-34 as a Novel Mediator Linking Vitamin D Deficiency with Osteoporosis and Knee Osteoarthritis.

Journal: International journal of molecular sciences

Published: September 26, 2025

Bi-allelic variants in NRDC cause a neurodevelopmental disorder characterized by neonatal lethality, microcephaly, and brain abnormalities.

Bi-allelic variants in NRDC cause a neurodevelopmental disorder characterized by neonatal lethality, microcephaly, and brain abnormalities.

Journal: American journal of human genetics

Published: July 19, 2025

Metabolic and Inflammatory Biomarkers Predicting Sarcopenic Obesity and Cardiometabolic Risk in Arab Women: A Cross-Sectional Study.

Metabolic and Inflammatory Biomarkers Predicting Sarcopenic Obesity and Cardiometabolic Risk in Arab Women: A Cross-Sectional Study.

Journal: International journal of molecular sciences

Published: April 29, 2025

Blurring the Lines: Co-Occurrence of MSH6 Variant and MLH1 Constitutional Epimutation in a Young Colorectal Cancer Patient.

Blurring the Lines: Co-Occurrence of MSH6 Variant and MLH1 Constitutional Epimutation in a Young Colorectal Cancer Patient.

Journal: Clinical genetics

Published: April 19, 2025

Executive Functions, Anxiety, Social Participation and Quality of Life in Children with Migraine During COVID-19.

Executive Functions, Anxiety, Social Participation and Quality of Life in Children with Migraine During COVID-19.

Journal: Life (Basel, Switzerland)

Published: March 06, 2025

Mono and Biallelic Variants in TRIM63 Are Frequently Associated With a Unique Form of Hypertrophic Cardiomyopathy.

Mono and Biallelic Variants in TRIM63 Are Frequently Associated With a Unique Form of Hypertrophic Cardiomyopathy.

Journal: Circulation. Genomic and precision medicine

Published: January 27, 2025

Sengers syndrome caused by biallelic TIMM29 variants and RNAi silencing in Drosophila orthologue recapitulates the human phenotype.

Sengers syndrome caused by biallelic TIMM29 variants and RNAi silencing in Drosophila orthologue recapitulates the human phenotype.

Journal: Human genomics

Published: November 01, 2024

A founder variant in TBCB is associated with global developmental delay, autism spectrum, and spastic paraparesis.

A founder variant in TBCB is associated with global developmental delay, autism spectrum, and spastic paraparesis.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 31, 2024

Characterization of severe COL6-related dystrophy due to the recurrent variant COL6A1 c.930+189C>T.

Characterization of severe COL6-related dystrophy due to the recurrent variant COL6A1 c.930+189C>T.

Journal: Brain : a journal of neurology

Published: October 03, 2024

Common Genetic Factors May Play a Role in the Relationships Between Body Composition, Adipokines, and Low-Back-Pain-Related Disability.

Common Genetic Factors May Play a Role in the Relationships Between Body Composition, Adipokines, and Low-Back-Pain-Related Disability.

Journal: Biomolecules

Published: September 25, 2024

Clinical profiling and medical management of Israeli individuals with Phelan McDermid syndrome.

Clinical profiling and medical management of Israeli individuals with Phelan McDermid syndrome.

Journal: Orphanet journal of rare diseases

Published: August 24, 2024

Showing 1-12 of 48

Last Updated: 09/26/2026