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Genetic Breast Cancer Susceptibility Variants and Prognosis in the Prospectively Randomized SUCCESS A Study.

Geburtshilfe und Frauenheilkunde·2017

Identification of candidate genes for prostate cancer-risk SNPs utilizing a normal prostate tissue eQTL data set.

Nature communications·2015

Genetic markers associated with abstinence length in alcohol-dependent subjects treated with acamprosate.

Translational psychiatry·2014

Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer.

Clinical genetics·2014

AIP inactivation leads to pituitary tumorigenesis through defective Gαi-cAMP signaling.

Oncogene·2014

Safety and efficacy of AAV-based mini- and micro-dystrophin gene therapies in Duchenne muscular dystrophy: a systematic review and meta-analysis of clinical trials.

Journal of medical genetics·2026

Phenotypic manifestations and variant reclassification of germline PTEN variants: a nationwide Danish study.

Journal of medical genetics·2026

Solid tumours in RASopathies: insights from a large monocentric cohort and systematic review of the literature.

Journal of medical genetics·2026

Hypertrophic cardiomyopathy: a genome-wide association meta-analysis and polygenic risk score.

Journal of medical genetics·2026

Exome sequencing and large-scale analysis of electronic medical record-linked biobank data identify candidate deafness genes.

Journal of medical genetics·2026

Exploring the clinical and mutational spectrum of MORC2-associated disorders.

Journal of medical genetics·2026

The Efficiency of Capillarys 2 Flex Piercing, Premier Resolution-HPLC, and VARIANT II-HPLC for Hemoglobin Constant Spring Detection.

Hemoglobin·2026

Case Report of Initial Manifestation of Hypogonadotropic Hypogonadism Based on Unoccluded Growth Plates in a 26-Year-Old Vietnamese Patient.

Cureus·2026

Clinical features of hereditary adrenocortical unresponsiveness to adrenocorticotropin (HAUA) in Japan: from a nationwide questionnaire based survey.

Endocrine journal·2026

Gastroduodenal Perforation Secondary to Heterotopic Pancreas in a Patient With Systemic Amyloidosis and End-Stage Renal Disease on Hemodialysis: A Case Report.

Cureus·2026

A Case of Convexity Meningioma Presenting With Acute Subdural Hematoma: A Case Report With a Pooled Analysis of 63 Reported Cases.

Cureus·2026

Hypothenar hammer syndrome: An expanded Kaji angiographic classification based on 91 cases.

Journal of plastic, reconstructive & aesthetic surgery : JPRAS·2026

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No fumarate hydratase (FH) mutations in hereditary prostate cancer

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Germline variants in IL4, MGMT and AKT1 are associated with prostate cancer-specific mortality: An analysis of 12,082 prostate cancer cases.

Genetic Breast Cancer Susceptibility Variants and Prognosis in the Prospectively Randomized SUCCESS A Study.

Identification of candidate genes for prostate cancer-risk SNPs utilizing a normal prostate tissue eQTL data set.

Genetic markers associated with abstinence length in alcohol-dependent subjects treated with acamprosate.

Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer.

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Safety and efficacy of AAV-based mini- and micro-dystrophin gene therapies in Duchenne muscular dystrophy: a systematic review and meta-analysis of clinical trials.

Phenotypic manifestations and variant reclassification of germline PTEN variants: a nationwide Danish study.

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No fumarate hydratase (FH) mutations in hereditary prostate cancer

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