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Association between genetic predisposition and disease burden of stroke in China: a genetic epidemiological study

• Authors : Huang, Qiya; Lan, Xianmei; Chen, Hebing

• Source: The Lancet Regional Health - Western Pacific ; volume 36, page 100779 ; ISSN 2666-6065

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Trans-ancestry genome-wide study of depression identifies 697 associations implicating cell types and pharmacotherapies

• Authors : Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium;

Subjects: Geðsjúkdómafræði; depression; drugs

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Non-Hotspot PIK3CA Variants Have Higher Variant Allele Frequency and are More Common in Syndromic Vascular Malformations.

• Authors : Andreoti, Themis-Areti A; Maiolo, Massimo; Tuleja, Aleksandra ...

Subjects: Humans; Class I Phosphatidylinositol 3-Kinases; Vascular Malformations

• Source: American journal of medical genetics. Part A, Vol. 197, no.2, p. e63883 [1-14] (2025)

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A multi-ancestry genome-wide association study identifies novel candidate loci in the RARB gene associated with hypertensive disorders of pregnancy.

• Authors : Mack, Jasmine A; Burkholder, Adam; Akhtari, Farida S

Subjects: Personalized Environment and Genes Study (PEGS); UK Biobank; genome-wide associateion study (GWAS)

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Human Genetic Evidence to Inform Clinical Development of IL-6 Signaling Inhibition for Abdominal Aortic Aneurysm.

• Authors : Burgess, Stephen; Cronjé, Héléne T; deGoma, Emil

Subjects: aortic aneurysm; abdominal; thoracic

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Non-Hotspot PIK3CA Variants Have Higher Variant Allele Frequency and are More Common in Syndromic Vascular Malformations.

• Authors : Andreoti, Themis-Areti A; Maiolo, Massimo; Tuleja, Aleksandra ...

Subjects: Humans; Class I Phosphatidylinositol 3-Kinases; Vascular Malformations

• Source: American journal of medical genetics. Part A, Vol. 197, no.2, p. e63883 [1-14] (2025)

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The NHS England Jewish BRCA Testing Programme:overview after first year of implementation (2023-2024)

• Authors : Torr, Bethany; Bell, Nicola; McCarthy, Ruth

Subjects: Humans; Jews/genetics; Female

• Source: Torr , B , Bell , N , McCarthy , R , Hamill , M , Nolan , J , Muralidharan , S , Andrews , C , Valganon-Petrizan , M , Clinch , Y , MacMahon , S , Morilla , A , George , A , Ryves , P , Dasani , P ,

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Functionally characterizing obesity-susceptibility genes using CRISPR/Cas9, in vivo imaging and deep learning

• Authors : Mazzaferro, Eugenia; Mujica, Endrina; Zhang, Hanqing

Subjects: Animals; Zebrafish/genetics; CRISPR-Cas Systems

• Source: Mazzaferro , E , Mujica , E , Zhang , H , Emmanouilidou , A , Jenseit , A , Evcimen , B , Metzendorf , C , Dethlefsen , O , Loos , R J , Vienberg , S G , Larsson , A , Allalou , A & den Hoed , M 2025

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Characterizing the Genetic Basis for Inherited Retinal Disease: Lessons Learned From the Foundation Fighting Blindness Clinical Consortiums Gene Poll.

• Authors : Branham, Kari; Samarakoon, Lassana; Audo, Isabelle

Subjects: Humans; Retinal Diseases; Genetic Testing

• Source: Investigative Ophthalmology & Visual Science, vol 66, iss 2

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Evaluation of Multiple Breast Cancer Polygenic Risk Score Panels in Women of Latin American Heritage.

• Authors : Huang, Xiaosong; Lott, Paul; Hu, Donglei

Subjects: Humans; Female; Breast Neoplasms

• Source: Cancer Epidemiology, Biomarkers & Prevention, vol 34, iss 2

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