Busra Gizem Kina

ORCID: 0000-0001-6013-1035 · 2 papers in corpus

article 2023

Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family

Molecular genetics & genomic medicine ·doi:10.1002/mgg3.2312

BACKGROUND: Endometriosis is an estrogen-dependent, chronic inflammatory disease that affects 10% of women during the reproductive ages. Despite the estimated 50% heritability for the condition, only 26% was associated with common genetic v…

article 2022

P-301 Exome sequencing reveals novel candidate variants for endometriosis and endometrial serous adenocarcinoma in a single family having multiple affected members

·doi:10.1093/humrep/deac107.287

Abstract Study question Could genetic evaluation of a family, having multiple affected members with endometriosis, contribute to identifying novel rare variants for the missing heritability of the disease? Summary answer Two novel genetic v…