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Journal Articles

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

Frank Rühle, Anika Witten, Andrei Barysenka, Andreas Huge, Astrid Arning, Christine Heller, Anne Krümpel, Rolf Mesters, Andre Franke, Wolfgang Lieb, Mona Riemenschneider, Milan Hiersche, Verena Limperger, Ulrike Nowak-Göttl, Monika Stoll

Blood (2017) 129 (6): 783–790.

https://doi.org/10.1182/blood-2016-07-728840

Published: 2017

Includes: Supplemental data

Journal Articles

DNA methylation changes are a late event in acute promyelocytic leukemia and coincide with loss of transcription factor binding

Blood (2013) 121 (1): 178–187.

https://doi.org/10.1182/blood-2012-08-448860

Published: 2013

Includes: Supplemental data

Journal Articles

A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke

Astrid Arning, Milan Hiersche, Anika Witten, Gerhard Kurlemann, Karin Kurnik, Daniela Manner, Monika Stoll, Ulrike Nowak-Göttl

Blood (2012) 120 (26): 5231–5236.

https://doi.org/10.1182/blood-2012-07-442038

Published: 2012

Includes: Supplemental data

Journal Articles

Identification of the PML-RARα Associated DNA Methylome Using Reduced Representation Bisulfite Sequencing in Primary Patient Samples

Christian Rohde, PhD, Till Schoofs, Katja Hebestreit, Hans-Ulrich Klein, PhD, Anika Witten, PhD, Monika Stoll, PhD, Eva Lengfelder, MD, Wolf-Karsten Hofmann, MD, Peter Schlenke, PhD, Stefanie Göllner, PhD, Thomas Büchner, MD, Maria Cristina Sauerland, Steffen Koschmieder, MD, Wolfgang E. Berdel, Martin Dugas, MD, Carsten Müller-Tidow, MD

Blood (2011) 118 (21): 2436.

https://doi.org/10.1182/blood.V118.21.2436.2436

Published: 2011

Journal Articles

A Distinct DNA Methylation Pattern Characterizes Childhood Acute Lymphoblastic Leukemia and Separates Patients Into Prognostic Groups,

Stefanie Göllner, PhD, Anika Witten, PhD, Monika Stoll, PhD, Wolfgang E. Berdel, Martin Schrappe, MD, Gunnar Cario, MD, Martin Stanulla, MD, MSc, Carsten Müller-Tidow, MD

Blood (2011) 118 (21): 3568.

https://doi.org/10.1182/blood.V118.21.3568.3568

Published: 2011

NARROW

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

DNA methylation changes are a late event in acute promyelocytic leukemia and coincide with loss of transcription factor binding

A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke

Identification of the PML-RARα Associated DNA Methylome Using Reduced Representation Bisulfite Sequencing in Primary Patient Samples

A Distinct DNA Methylation Pattern Characterizes Childhood Acute Lymphoblastic Leukemia and Separates Patients Into Prognostic Groups,

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ASH Publications

American Society of Hematology

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

DNA methylation changes are a late event in acute promyelocytic leukemia and coincide with loss of transcription factor binding

A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke

Identification of the PML-RARα Associated DNA Methylome Using Reduced Representation Bisulfite Sequencing in Primary Patient Samples

A Distinct DNA Methylation Pattern Characterizes Childhood Acute Lymphoblastic Leukemia and Separates Patients Into Prognostic Groups,

Email alerts

ASH Publications

American Society of Hematology

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