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Journal Articles

Clinical Consequences of Rare Germline Variation in Genes Associated with Coagulation across 451,958 Individuals

Justine Ryu, Amelia K Haj, Satoshi Koyama, Sean J. Jurgens, Simone Sanna-Cherchi, Patrick Ellinor, Pavan K Bendapudi

Blood (2023) 142 (Supplement 1): 3972.

https://doi.org/10.1182/blood-2023-186786

Published: 2023

Journal Articles

Coagulation Factor XII ( F12 ) Haploinsufficiency Is Protective Against Venous Thromboembolism in 415,921 Individuals

Amelia K Haj, Justine Ryu, Satoshi Koyama, Sean J. Jurgens, Xin Wang, Seung Hoan Choi, Sharjeel Chaudhry, Simone Sanna-Cherchi, Steven P Grover, Patrick Ellinor, Pavan K Bendapudi

Blood (2023) 142 (Supplement 1): 805.

https://doi.org/10.1182/blood-2023-189823

Published: 2023

Journal Articles

Rare Germline Loss-of-Function Variants in HSP47 ( SERPINH1 ) Are Associated with an Intermediate Osteogenesis Imperfecta Phenotype Characterized By Atopic Inflammation and Increased Risk of Thrombosis

Amelia K Haj, Sean J. Jurgens, Xin Wang, Justine Ryu, Seung Hoan Choi, Steven P Grover, Simone Sanna-Cherchi, Alec A Schmaier, Patrick Ellinor, Pavan K Bendapudi

Blood (2023) 142 (Supplement 1): 3934.

https://doi.org/10.1182/blood-2023-189896

Published: 2023

Journal Articles

Protein Z ( PROZ ) Loss of Function Is Associated with Increased Risk of Ischemic Stroke in 416,767 UK Biobank Participants

Amelia K Haj, Sean J. Jurgens, Xin Wang, Justine Ryu, Seung Hoan Choi, Simone Sanna-Cherchi, Patrick Ellinor, Pavan K Bendapudi

Blood (2023) 142 (Supplement 1): 2611.

https://doi.org/10.1182/blood-2023-182861

Published: 2023

Journal Articles

Meta-Analysis of National-Level Genotyping Datasets to Determine the Risk of Thrombosis in Double Heterozygous Carriers of Factor V Leiden and the Prothrombin G20210A Mutation across 876,417 Individuals

Justine Ryu, Joel Rämö, Sean J. Jurgens, Teemu Niiranen, Aarno Palotie, Mark Daly, Simone Sanna-Cherchi, Patrick Ellinor, Kenneth A Bauer, Pavan K Bendapudi

Blood (2023) 142 (Supplement 1): 806.

https://doi.org/10.1182/blood-2023-187105

Published: 2023

NARROW

Clinical Consequences of Rare Germline Variation in Genes Associated with Coagulation across 451,958 Individuals

Coagulation Factor XII ( F12 ) Haploinsufficiency Is Protective Against Venous Thromboembolism in 415,921 Individuals

Rare Germline Loss-of-Function Variants in HSP47 ( SERPINH1 ) Are Associated with an Intermediate Osteogenesis Imperfecta Phenotype Characterized By Atopic Inflammation and Increased Risk of Thrombosis

Protein Z ( PROZ ) Loss of Function Is Associated with Increased Risk of Ischemic Stroke in 416,767 UK Biobank Participants

Meta-Analysis of National-Level Genotyping Datasets to Determine the Risk of Thrombosis in Double Heterozygous Carriers of Factor V Leiden and the Prothrombin G20210A Mutation across 876,417 Individuals

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ASH Publications

American Society of Hematology

Clinical Consequences of Rare Germline Variation in Genes Associated with Coagulation across 451,958 Individuals

Coagulation Factor XII ( F12 ) Haploinsufficiency Is Protective Against Venous Thromboembolism in 415,921 Individuals

Rare Germline Loss-of-Function Variants in HSP47 ( SERPINH1 ) Are Associated with an Intermediate Osteogenesis Imperfecta Phenotype Characterized By Atopic Inflammation and Increased Risk of Thrombosis

Protein Z ( PROZ ) Loss of Function Is Associated with Increased Risk of Ischemic Stroke in 416,767 UK Biobank Participants

Meta-Analysis of National-Level Genotyping Datasets to Determine the Risk of Thrombosis in Double Heterozygous Carriers of Factor V Leiden and the Prothrombin G20210A Mutation across 876,417 Individuals

Email alerts

ASH Publications

American Society of Hematology

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