Karima Sifi - Publications

Primary ovarian insufficiency due to homozygous variants in the homeobox transcription factor NOBOX.

Journal: Molecular biology reports

Published: August 26, 2025

Association between C677T variant of methylene tetrahydrofolate reductase and hypospadias risk in Algeria.

Journal: The Turkish journal of pediatrics

Published: March 15, 2025

Association of angiotensin-converting enzyme gene insertion/deletion polymorphism (rs4646994) with schizophrenia in an eastern Algerian population: a case-control study.

Journal: The Pan African medical journal

Published: January 28, 2025

Investigation of Y chromosome microdeletions in algerian children with hypospadias.

Journal: Journal of pediatric urology

Published: October 19, 2024

Novel Genomic Variants, Atypical Phenotypes and Evidence of a Digenic/Oligogenic Contribution to Disorders/Differences of Sex Development in a Large North African Cohort.

Journal: Frontiers in genetics

Published: March 20, 2022

Expanding DSD Phenotypes Associated with Variants in the DEAH-Box RNA Helicase DHX37.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation

Published: January 04, 2021

Angiotensin-converting enzyme insertion/deletion gene polymorphisms and the risk of glioma in an Algerian population.

Journal: The Pan African medical journal

Published: February 11, 2018

γ-sarcoglycan and dystrophin mutation spectrum in an Algerian cohort.

Journal: Muscle & nerve

Published: April 21, 2016