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UnknownUnraveling the genetic background of individuals with a clinical familial hypercholesterolemia phenotype.
Not available
S-EPMC10832474 | biostudies-literature
UnknownCommon genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility.
Not available
S-EPMC9546047 | biostudies-literature
UnknownTrans-ethnic GWAS meta-analysis of idiopathic spermatogenic failure highlights the immune-mediated nature of Sertoli cell-only syndrome.
Not available
S-EPMC11972312 | biostudies-literature
UnknownEvaluation of Male Fertility-Associated Loci in a European Population of Patients with Severe Spermatogenic Impairment.
Not available
S-EPMC7823507 | biostudies-literature
UnknownContribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia.
Not available
S-EPMC9797780 | biostudies-literature
UnknownImmune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility.
Not available
S-EPMC9649734 | biostudies-literature
UnknownCommon Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome.
Not available
S-EPMC9225465 | biostudies-literature
UnknownA comprehensive study of common and rare genetic variants in spermatogenesis-related loci identifies new risk factors for idiopathic severe spermatogenic failure.
Not available
S-EPMC11645127 | biostudies-literature
UnknownHeterogeneous contributions of change in population distribution of body mass index to change in obesity and underweight.
Not available
S-EPMC7943191 | biostudies-literature
UnknownGlobal anaesthesia practice using inguinal hernia surgery as a tracer condition: a secondary analysis of an international prospective cohort study.
Not available
S-EPMC12519944 | biostudies-literature
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