Shantel Weinsheimer

University of California San Francisco

H指数:31

被引数:8,212

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Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis (vol 111, pg 2283, 2024)

遗传性出血性毛细血管扩张症动静脉畸形的体细胞突变支持双等位基因两击突变的发病机制 (111卷，2283页，2024页)

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2025-04-010

PRE

Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2024-10-012

PRE

Clinical segmentation in 22q11.2 deletion syndrome: Cognitive impairments and additional genetic load

JOURNAL OF PSYCHIATRIC RESEARCH

IF3.2

2024-09-010

PRE

Mild Hypoxia Accelerates Cerebral Cavernous Malformation Disease Through CX3CR1-CX3CL1 Signaling

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

IF7.4

2024-06-012

PRE

Frias-Anaya, Eduardo; Gallego-Gutierrez, Helios; Gongol, Brendan; Weinsheimer, Shantel; Lai, Catherine Chinhchu; Orecchioni, Marco; Sriram, Aditya; Bui, Cassandra M.; Nelsen, Bliss; Hale, Preston; Pham, Angela; Shenkar, Robert; DeBiasse, Dorothy; Lightle, Rhonda; Girard, Romuald; Li, Ying; Srinath, Abhinav; Daneman, Richard; Nudleman, Eric; Sun, Hao; Guma, Monica; Dubrac, Alexandre; Mesarwi, Omar A.; Ley, Klaus; Kim, Helen; Awad, Issam A.; Ginsberg, Mark H.; Lopez-Ramirez, Miguel Alejandro

Longitudinal Risk of Seizures in Patients With Brain Arteriovenous Malformations

STROKE

IF8.9

2024-02-010

PRE

Identification of Circulating Epigenetic Biomarkers for Seizure in Brain Arteriovenous Malformation by Methylome Profiling

STROKE

IF8.9

2024-02-010

PRE

Increased Collagen I/Collagen III Ratio is Associated With Hemorrhage in Brain Arteriovenous Malformations in Human and Mouse

STROKE