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Journal Articles

How Morphologic Features Are Shaped By Underlying Somatic Genotype in MDS

Yasunobu Nagata, MD PhD, Ran Zhao, Hassan Awada, Cassandra M Kerr, MS, Abhinav Goyal, Inom Mirzaev, Sunisa Kongkiatkamon, Aziz Nazha, MD, Tomas Radivoyevitch, PhD, Jacob Scott, MD, Mikkael A. Sekeres, MD MS, Brian P. Hobbs, PhD, Jaroslaw P. Maciejewski, MD PhD
Journal: Blood
Blood (2019) 134 (Supplement_1): 1716.
https://doi.org/10.1182/blood-2019-127285
Published: 2019
Journal Articles

Splicing Control in Normal and Aberrant Erythropoiesis

Esther Obeng, MD PhD
Journal: Blood
Blood (2018) 132 (Supplement 1): SCI-47.
https://doi.org/10.1182/blood-2018-99-109414
Published: 2018
Journal Articles

Non-Random Interactions between Founder and Subclonal Mutations Shape the Clinical and Morphological Features of MDS

Yasunobu Nagata, MD PhD, Hideki Makishima, MD PhD, Cassandra M. Hirsch, BS, Mai Aly, MD, Abhinav Goyal, MD, Hassan Awada, MD, Mohammad Fahad B Asad, MD MBBS, Teodora Kuzmanovic, BA, Bartlomiej P. Przychodzen, MSc, Hiromichi Suzuki, MD , PhD, Tetsuichi Yoshizato, MD,PhD, Kenichi Yoshida, MD PhD, Kenichi Chiba, B.A., Hiroko Tanaka, B.A., Yuichi Shiraishi, PhD, Satoru Miyano, PhD, Sudipto Mukherjee, MD PhD MPH, Tomas Radivoyevitch, PhD, Thomas Laframboise, PhD, Aziz Nazha, MD, Mikkael A. Sekeres, MD MS, Torsten Haferlach, MD, Seishi Ogawa, MD PhD, Jaroslaw P. Maciejewski, PhD MD FACP
Journal: Blood
Blood (2017) 130 (Supplement 1): 583.
https://doi.org/10.1182/blood.V130.Suppl_1.583.583
Published: 2017
Journal Articles

How Somatic Mutations Carve Morphologic Imprint in MDS?

Abhinav Goyal, MD, Mohammad Fahad B Asad, MD MBBS, Hassan Awada, MD, Mai Aly, MD, Cassandra M. Hirsch, BS, Bartlomiej P. Przychodzen, MSc, Tomas Radivoyevitch, PhD, Aziz Nazha, MD, Sudipto Mukherjee, MD PhD MPH, Mikkael A. Sekeres, MD MS, Jaroslaw P. Maciejewski, PhD MD FACP, Yasunobu Nagata, MD PhD
Journal: Blood
Blood (2017) 130 (Supplement 1): 2949.
https://doi.org/10.1182/blood.V130.Suppl_1.2949.2949
Published: 2017
Journal Articles

Genotype/Phenotype Correlations in 103 Children from 87 Families with Hereditary Spherocytosis

Jakob Pugi, BSc, Luke J. Drury, PhDBS, Jacob C. Langer, MD FRCSC, Sheila Butchart, BScN, RN, Michelle Fantauzzi, BScN, RN, Jillian Baker, MD MSc, Victor S. Blanchette, FRCP, FRCPC, Melanie Ann Kirby-Allen, MD FRCPC, MBBS, Manuel Carcao, MD
Journal: Blood
Blood (2016) 128 (22): 2432.
https://doi.org/10.1182/blood.V128.22.2432.2432
Published: 2016
Journal Articles

Genotype Phenotype Correlation in Patients with aHUS and Abnormal Genetic Studies: A Single Centre Experience

Katerina Pavenski, MD FRCP, Jerome M. Teitel, MD, Gloria Lim, BSc, MSc, MD, Michelle Sholzberg, MD, Michael Kirschfink, Christoph Licht, MD FRCP(C), FASN
Journal: Blood
Blood (2014) 124 (21): 4186.
https://doi.org/10.1182/blood.V124.21.4186.4186
Published: 2014
Journal Articles

Disruption of the ASXL1 Gene Is Prevalent In PMF: Analysis of Molecular Genetics and Clinical Phenotypes

Brady L Stein, MD, Donna M Williams, PhD, Michael A McDevitt, MD, PhD, Christine L. O'Keefe, PhD, Ophelia Rogers, Jerry L Spivak, Jaroslaw Maciejewski, Alison R Moliterno, MD
Journal: Blood
Blood (2010) 116 (21): 3074.
https://doi.org/10.1182/blood.V116.21.3074.3074
Published: 2010
Journal Articles

Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations

Brief Report
Manuela Germeshausen, Magda Grudzien, Cornelia Zeidler, Hengameh Abdollahpour, Sevgi Yetgin, Nima Rezaei, Matthias Ballmaier, Bodo Grimbacher, Karl Welte, Christoph Klein
Journal: Blood
Blood (2008) 111 (10): 4954–4957.
https://doi.org/10.1182/blood-2007-11-120667
Published: 2008
Journal Articles

Genotype-Phenotype Associations in Patients with Severe Congenital Neutropenia.

Philip S. Rosenberg, PhD, Steven Stein, M.D., Elin Rodger, Audrey Anna Bolyard, R.N.,B.S., Mary Ann Bonilla, M.D., Yigal Dror, M.D., George Kannourakis, M.D., Peter E. Newburger, M.D., Laurence A. Boxer, M.D., Blanche P. Alter, M.D.,M.P.H., David C. Dale, M.D.
Journal: Blood
Blood (2006) 108 (11): 502.
https://doi.org/10.1182/blood.V108.11.502.502
Published: 2006
Journal Articles

Genotype Phenotype Correlation in Thalassemia Syndromes and Their Correlation with Xmn-1 Polymorphism.

Anupam Sachdeva, MD, Aditya Raina, DNB, Varinder Kumar Khanna, MD, Subhash Chander Arya, DABP, Satya Prakash Yadav, DNB, Ishwar Verma, MD
Journal: Blood
Blood (2005) 106 (11): 3845.
https://doi.org/10.1182/blood.V106.11.3845.3845
Published: 2005
Journal Articles

Genotype/Phenotype Correlations for Coagulation Factor XIII: Specific Normal Polymorphisms Are Associated With High or Low Factor XIII Specific Activity

Rashida Anwar, Louise Gallivan, Stuart D. Edmonds, Alexander F. Markham
Journal: Blood
Blood (1999) 93 (3): 897–905.
https://doi.org/10.1182/blood.V93.3.897
Published: 1999