Busra Gizem Kina

ORCID: 0000-0001-6013-1035 · 2 papers in corpus · active 2022-2023

Study types

  • article 2

Condition tags

  • endometriosis 2
  • infertility 2
  • dysmenorrhea 1
  • chronic_pelvic_pain 1
  • endometrioma 1
  • dyspareunia 1
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…