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Journal Articles

Neutropenia-Associated Mutations Differentially Impact Developmental Cell-States

David Muench, BS, Kyle Ferchen, BS, Giang Pham, PhD, Somchai Chutipongtanate, MDPhD, Pankaj Dwivedi, PhD, Stuart Hay, Kashish Chetal, MS, Jayati Mookerjee-Basu, PhD, Kejian Zhang, MD MBA, Kasiani C. Myers, MD, Kristopher Nazor, PhD, Kenneth D Greis, PhD, Dietmar J Kappes, PhD, Sing Sing Way, MDPhD, Nathan Salomonis, PhD, H. Leighton Grimes, PhD

Blood (2018) 132 (Supplement 1): 18.

https://doi.org/10.1182/blood-2018-99-116549

Published: 2018

Journal Articles

The First Registry for Patients with Congenital Dyserythropoietic Anemia in North America: Design and Preliminary Results

Blood (2017) 130 (Supplement 1): 2210.

https://doi.org/10.1182/blood.V130.Suppl_1.2210.2210

Published: 2017

Journal Articles

Plasminogen Activator Inhibitor Type 1 (PAI-1) and Thrombophilia: A 10 Year Retrospective Review of Clinical Data at a Large Children's Hospital

Triston Burnham, Joseph S. Palumbo, MD, Jennifer Pomales, RN, BSN, NE-BC, CPHON, Adam Lane, Rachel Brockhage, Kejian Zhang, MD MBA, Lori Luchtman-Jones, MD

Blood (2017) 130 (Supplement 1): 1069.

https://doi.org/10.1182/blood.V130.Suppl_1.1069.1069

Published: 2017

Journal Articles

HIF1A Is a Critical Downstream Mediator for Hemophagocytic Lymphohistiocytosis

Blood (2017) 130 (Supplement 1): 3565.

https://doi.org/10.1182/blood.V130.Suppl_1.3565.3565

Published: 2017

Journal Articles

VPS4A : A Novel Candidate Gene for Congenital Dyserythropoietic Anemia

Katie Giger, PhD, Georgios E Christakopoulos, MD, Lisa Trump, Clarissa E. Johnson, MD, Haripriya Sakthivel, Mary Risinger, Omar Niss, MD, Kejian Zhang, MD MBA, Lionel Blanc, PhD, Robert B. Lorsbach, MD PhD, Paritha I. Arumugam, PhD, Carolyn Lutzko, PhD, Theodosia A. Kalfa, MD PhD

Blood (2017) 130 (Supplement 1): 923.

https://doi.org/10.1182/blood.V130.Suppl_1.923.923

Published: 2017

Journal Articles

Perforin and CD107a testing is superior to NK cell function testing for screening patients for genetic HLH

Tamar S. Rubin, Kejian Zhang, Carrie Gifford, Adam Lane, Sharon Choo, Jack J. Bleesing, Rebecca A. Marsh

Blood (2017) 129 (22): 2993–2999.

https://doi.org/10.1182/blood-2016-12-753830

Published: 2017

Includes: Supplemental data

Journal Articles

Clinical Application of Massively Parallel Sequencing in the Diagnosis of Hereditary Hemolytic and Dyserythropoietic Anemias

Harry Lesmana, MD, Georgios E Christakopoulos, MD, Katie Giger Seu, PhD, Mary Risinger, PhD, Hatice Duzkale, MD MPH, PhD, Neha Dagaonkar, Kejian Zhang, MD, Theodosia A Kalfa, MD PhD

Blood (2016) 128 (22): 4746.

https://doi.org/10.1182/blood.V128.22.4746.4746

Published: 2016

Journal Articles

Cellular Hydration and Oxidation As Phenotype Modifiers in Sickle Cell Anemia

Mary A Risinger, PhD, Neha Dagaonkar, Georgios E Christakopoulos, MD, Jie Liu, PhD, Katie Giger Seu, PhD, Diamantis G Konstantinidis, BSc, PhD, Charles T Quinn, MD, Satheesh Chonat, MD, Clinton H Joiner, MD PhD, Kejian Zhang, MD, Theodosia A Kalfa, MD PhD

Blood (2016) 128 (22): 2446.

https://doi.org/10.1182/blood.V128.22.2446.2446

Published: 2016

Journal Articles

The genetic fingerprint of susceptibility for transplant-associated thrombotic microangiopathy

Sonata Jodele, Kejian Zhang, Fanggeng Zou, Benjamin Laskin, Christopher E. Dandoy, Kasiani C. Myers, Adam Lane, Jaroslav Meller, Mario Medvedovic, Jenny Chen, Stella M. Davies

Blood (2016) 127 (8): 989–996.

https://doi.org/10.1182/blood-2015-08-663435

Published: 2016

Includes: Supplemental data

Journal Articles

The Spectrum of Alpha-Spectrin Associated Hereditary Spherocytosis

Satheesh Chonat, MD, Mary Risinger, Neha Dagaonkar, Tamara Maghathe, Jennifer Rothman, MD, Jessica Connor, Karen Kalinyak, MD, Amber H Begtrup, PhD, Kejian Zhang, MD MBA, Theodosia A. Kalfa, MD PhD

Blood (2015) 126 (23): 941.

https://doi.org/10.1182/blood.V126.23.941.941

Published: 2015

Journal Articles

Genetic Testing for the Diagnosis of Hemoglobinopathies Has Very High Clinical Utility

Charles T. Quinn, MD MS, Amber H Begtrup, PhD, Mary C. Paniagua, MA, Hatice Duzkale, MD MPH, PhD, Kejian Zhang, MD MBA

Blood (2015) 126 (23): 524.

https://doi.org/10.1182/blood.V126.23.524.524

Published: 2015

Journal Articles

Genotype-Phenotype Correlations in Hereditary Elliptocytosis (HE) and Hereditary Pyropoikilocytosis (HPP)

Omar Niss, MD, Satheesh Chonat, MD, Karol Kerr, MD, Patrick T. McGann, MD MS, Marya Obaid Almansoori, MD, Maa-Ohui Quarmyne, MBChB MS, Kejian Zhang, MD MBA, Theodosia A. Kalfa, MD PhD

Blood (2015) 126 (23): 3344.

https://doi.org/10.1182/blood.V126.23.3344.3344

Published: 2015

Journal Articles

Alu-Element Insertion in Pklr Gene As a Novel Cause of Severe Hereditary Nonspherocytic Hemolytic Anemia

Harry Lesmana, MD, Lisa Dyer, PhD, Ping Zhou, Xia Li, PhD, James Denton, MS, Satheesh Chonat, MD, Kejian Zhang, MD MBA, Robert J. Hopkin, MD, Theodosia A. Kalfa, MD PhD

Blood (2015) 126 (23): 3349.

https://doi.org/10.1182/blood.V126.23.3349.3349

Published: 2015

Journal Articles

Accuracy of flow cytometric perforin screening for detecting patients with FHL due to PRF1 mutations

Manar Abdalgani, Alexandra H. Filipovich, Sharon Choo, Kejian Zhang, Carrie Gifford, Joyce Villanueva, Jack J. Bleesing, Rebecca A. Marsh

Blood (2015) 126 (15): 1858–1860.

https://doi.org/10.1182/blood-2015-06-648659

Published: 2015

Includes: Supplemental data

Journal Articles

Hemophagocytic lymphohistiocytosis caused by dominant-negative mutations in STXBP2 that inhibit SNARE-mediated membrane fusion

Waldo A. Spessott, Maria L. Sanmillan, Margaret E. McCormick, Nishant Patel, Joyce Villanueva, Kejian Zhang, Kim E. Nichols, Claudio G. Giraudo

Blood (2015) 125 (10): 1566–1577.

https://doi.org/10.1182/blood-2014-11-610816

Published: 2015

Includes: Supplemental data

Journal Articles

Synergistic defects of different molecules in the cytotoxic pathway lead to clinical familial hemophagocytic lymphohistiocytosis

Kejian Zhang, Shanmuganathan Chandrakasan, Heather Chapman, C. Alexander Valencia, Ammar Husami, Diane Kissell, Judith A. Johnson, Alexandra H. Filipovich

Blood (2014) 124 (8): 1331–1334.

https://doi.org/10.1182/blood-2014-05-573105

Published: 2014

Journal Articles

Misleading results from saliva samples of patients post-BMT in exome analyses

C. Alexander Valencia, Subba Rao Indugula, Abhinav Mathur, Chao Wei, Jenice Caitlin Brown, India Cole, Sarah Dell, Jessica Connor, Kejian Zhang

Blood (2014) 124 (4): 660–661.

https://doi.org/10.1182/blood-2014-04-572941

Published: 2014

Journal Articles

Development Of a Comprehensive Rapid Next-Generation Sequencing Assay For The Diagnosis Of Inherited Hemolytic Anemia

Amber Hogart Begtrup, PhD, Neha Dagaonkar, Suvarnamala Pushkaran, M.Sc., Katie M. Giger, PhD, Ammar Husami, Diane Kissell, Clinton H. Joiner, MD, PhD, Mehdi Keddache, Ph.D., Kejian Zhang, M.D., M.B.A., Theodosia A. Kalfa, M.D., Ph.D.

Blood (2013) 122 (21): 949.

https://doi.org/10.1182/blood.V122.21.949.949

Published: 2013

Journal Articles

Abnormalities in the alternative pathway of complement in children with hematopoietic stem cell transplant-associated thrombotic microangiopathy

Sonata Jodele, Christoph Licht, Jens Goebel, Bradley P. Dixon, Kejian Zhang, Theru A. Sivakumaran, Stella M. Davies, Fred G. Pluthero, Lily Lu, Benjamin L. Laskin

Blood (2013) 122 (12): 2003–2007.

https://doi.org/10.1182/blood-2013-05-501445

Published: 2013

Journal Articles

Gene-expression signatures differ between different clinical forms of familial hemophagocytic lymphohistiocytosis

Janos Sumegi, Shawnagay V. Nestheide, Michael G. Barnes, Joyce Villanueva, Kejian Zhang, Alexei A. Grom, Alexandra H. Filipovich

Blood (2013) 121 (7): e14–e24.

https://doi.org/10.1182/blood-2012-05-425769

Published: 2013

Includes: Supplemental data

NARROW

Neutropenia-Associated Mutations Differentially Impact Developmental Cell-States

The First Registry for Patients with Congenital Dyserythropoietic Anemia in North America: Design and Preliminary Results

Plasminogen Activator Inhibitor Type 1 (PAI-1) and Thrombophilia: A 10 Year Retrospective Review of Clinical Data at a Large Children's Hospital

HIF1A Is a Critical Downstream Mediator for Hemophagocytic Lymphohistiocytosis

VPS4A : A Novel Candidate Gene for Congenital Dyserythropoietic Anemia

Perforin and CD107a testing is superior to NK cell function testing for screening patients for genetic HLH

Clinical Application of Massively Parallel Sequencing in the Diagnosis of Hereditary Hemolytic and Dyserythropoietic Anemias

Cellular Hydration and Oxidation As Phenotype Modifiers in Sickle Cell Anemia

The genetic fingerprint of susceptibility for transplant-associated thrombotic microangiopathy

The Spectrum of Alpha-Spectrin Associated Hereditary Spherocytosis

Genetic Testing for the Diagnosis of Hemoglobinopathies Has Very High Clinical Utility

Genotype-Phenotype Correlations in Hereditary Elliptocytosis (HE) and Hereditary Pyropoikilocytosis (HPP)

Alu-Element Insertion in Pklr Gene As a Novel Cause of Severe Hereditary Nonspherocytic Hemolytic Anemia

Accuracy of flow cytometric perforin screening for detecting patients with FHL due to PRF1 mutations

Hemophagocytic lymphohistiocytosis caused by dominant-negative mutations in STXBP2 that inhibit SNARE-mediated membrane fusion

Synergistic defects of different molecules in the cytotoxic pathway lead to clinical familial hemophagocytic lymphohistiocytosis

Misleading results from saliva samples of patients post-BMT in exome analyses

Development Of a Comprehensive Rapid Next-Generation Sequencing Assay For The Diagnosis Of Inherited Hemolytic Anemia

Abnormalities in the alternative pathway of complement in children with hematopoietic stem cell transplant-associated thrombotic microangiopathy

Gene-expression signatures differ between different clinical forms of familial hemophagocytic lymphohistiocytosis

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American Society of Hematology

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ASH Publications

American Society of Hematology

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