Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism

Frank Ruehle; Anika Witten; Andrei Barysenka; Andreas Huge; Astrid Arning; Christine Heller; Anne Kruempel; Rolf Mesters; Andre Franke; Wolfgang Lieb; Mona Riemenschneider; Milan Hiersche; Verena Limperger; Ulrike Nowak-Goettl; Monika Stoll

doi:10.1182/blood-2016-07-728840

Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism

Frank Ruehle, Anika Witten, Andrei Barysenka, Andreas Huge, Astrid Arning, Christine Heller, Anne Kruempel, Rolf Mesters, Andre Franke, Wolfgang Lieb, Mona Riemenschneider, Milan Hiersche, Verena Limperger, Ulrike Nowak-Goettl, Monika Stoll^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

Original language	English
Pages (from-to)	783-790
Number of pages	8
Journal	Blood
Volume	129
Issue number	6
DOIs	https://doi.org/10.1182/blood-2016-07-728840
Publication status	Published - 9 Feb 2017

Keywords

GENOME-WIDE ASSOCIATION
ARTERIAL ISCHEMIC-STROKE
DNA-SEQUENCING DATA
FAMILY-BASED TESTS
THROMBOPHILIA
RISK
METAANALYSIS
RELEASE
LINKAGE
DISEQUILIBRIUM

Access to Document

10.1182/blood-2016-07-728840

Cite this

Ruehle, F., Witten, A., Barysenka, A., Huge, A., Arning, A., Heller, C., Kruempel, A., Mesters, R., Franke, A., Lieb, W., Riemenschneider, M., Hiersche, M., Limperger, V., Nowak-Goettl, U., & Stoll, M. (2017). Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism. Blood, 129(6), 783-790. https://doi.org/10.1182/blood-2016-07-728840

Ruehle, Frank ; Witten, Anika ; Barysenka, Andrei ; Huge, Andreas ; Arning, Astrid ; Heller, Christine ; Kruempel, Anne ; Mesters, Rolf ; Franke, Andre ; Lieb, Wolfgang ; Riemenschneider, Mona ; Hiersche, Milan ; Limperger, Verena ; Nowak-Goettl, Ulrike ; Stoll, Monika. / Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism. In: Blood. 2017 ; Vol. 129, No. 6. pp. 783-790.

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title = "Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism",

keywords = "GENOME-WIDE ASSOCIATION, ARTERIAL ISCHEMIC-STROKE, DNA-SEQUENCING DATA, FAMILY-BASED TESTS, THROMBOPHILIA, RISK, METAANALYSIS, RELEASE, LINKAGE, DISEQUILIBRIUM",

author = "Frank Ruehle and Anika Witten and Andrei Barysenka and Andreas Huge and Astrid Arning and Christine Heller and Anne Kruempel and Rolf Mesters and Andre Franke and Wolfgang Lieb and Mona Riemenschneider and Milan Hiersche and Verena Limperger and Ulrike Nowak-Goettl and Monika Stoll",

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doi = "10.1182/blood-2016-07-728840",

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journal = "Blood",

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Ruehle, F, Witten, A, Barysenka, A, Huge, A, Arning, A, Heller, C, Kruempel, A, Mesters, R, Franke, A, Lieb, W, Riemenschneider, M, Hiersche, M, Limperger, V, Nowak-Goettl, U & Stoll, M 2017, 'Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism', Blood, vol. 129, no. 6, pp. 783-790. https://doi.org/10.1182/blood-2016-07-728840

Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism. / Ruehle, Frank; Witten, Anika; Barysenka, Andrei; Huge, Andreas; Arning, Astrid; Heller, Christine; Kruempel, Anne; Mesters, Rolf; Franke, Andre; Lieb, Wolfgang; Riemenschneider, Mona; Hiersche, Milan; Limperger, Verena; Nowak-Goettl, Ulrike; Stoll, Monika.

In: Blood, Vol. 129, No. 6, 09.02.2017, p. 783-790.

Research output: Contribution to journal › Article › Academic › peer-review

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T1 - Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism

AU - Ruehle, Frank

AU - Witten, Anika

AU - Barysenka, Andrei

AU - Huge, Andreas

AU - Arning, Astrid

AU - Heller, Christine

AU - Kruempel, Anne

AU - Mesters, Rolf

AU - Franke, Andre

AU - Lieb, Wolfgang

AU - Riemenschneider, Mona

AU - Hiersche, Milan

AU - Limperger, Verena

AU - Nowak-Goettl, Ulrike

AU - Stoll, Monika

PY - 2017/2/9

Y1 - 2017/2/9

KW - GENOME-WIDE ASSOCIATION

KW - ARTERIAL ISCHEMIC-STROKE

KW - DNA-SEQUENCING DATA

KW - FAMILY-BASED TESTS

KW - THROMBOPHILIA

KW - RISK

KW - METAANALYSIS

KW - RELEASE

KW - LINKAGE

KW - DISEQUILIBRIUM

U2 - 10.1182/blood-2016-07-728840

DO - 10.1182/blood-2016-07-728840

M3 - Article

C2 - 28011674

VL - 129

SP - 783

EP - 790

JO - Blood

JF - Blood

SN - 0006-4971

IS - 6

ER -