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Journal Articles

Diagnostic guidelines for familial hemophagocytic lymphohistiocytosis revisited

Jan-Inge Henter, Elena Sieni, Julia Eriksson, Elisabet Bergsten, Ida Hed Myrberg, Scott W. Canna, Maria Luisa Coniglio, Randy Q. Cron, Kate F. Kernan, Ashish R. Kumar, Kai Lehmberg, Francesca Minoia, Ahmed Naqvi, Angelo Ravelli, Yong-Min Tang, Matteo Bottai, Yenan T. Bryceson, AnnaCarin Horne, Michael B. Jordan

Blood (2024) 144 (22): 2308–2318.

https://doi.org/10.1182/blood.2024025077

Published: 2024

Includes: Supplemental data

Journal Articles

Efficacy of T-cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosis

Blood (2024) 144 (8): 873–887.

https://doi.org/10.1182/blood.2024024499

Published: 2024

Includes: Supplemental data

Journal Articles

Comprehensive Exploration of NK Cell Education in ADCC Triggered By a Monoclonal Antibody or a Bispecific Killer Engager Molecule (BiKE)

Caroline Leijonhufvud, Heinrich Schlums, Arwen Stikvoort, Michael Uhlin, Yenan T Bryceson, Mattias Carlsten

Blood (2022) 140 (Supplement 1): 8350.

https://doi.org/10.1182/blood-2022-166470

Published: 2022

Journal Articles

RhoG deficiency abrogates cytotoxicity of human lymphocytes and causes hemophagocytic lymphohistiocytosis

Blood (2021) 137 (15): 2033–2045.

https://doi.org/10.1182/blood.2020008738

Published: 2021

Includes: Supplemental data

Journal Articles

HLH: genomics illuminates pathophysiological diversity

Bianca Tesi, Yenan T. Bryceson

Blood (2018) 132 (1): 5–7.

https://doi.org/10.1182/blood-2018-05-845818

Published: 2018

Journal Articles

Single-cell dissection of monosomy 7 syndromes

Irene Gutierrez-Perez, Yenan T. Bryceson

Blood (2017) 130 (25): 2693–2695.

https://doi.org/10.1182/blood-2017-11-811935

Published: 2017

Journal Articles

Constitutional SAMD9L Mutations Cause Familial Myelodisplastic Syndrome with Monosomy 7 and Stable Revertant Mosaicism

Blood (2017) 130 (Supplement 1): 1672.

https://doi.org/10.1182/blood.V130.Suppl_1.1672.1672

Published: 2017

Journal Articles

Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms

Blood (2017) 129 (16): 2266–2279.

https://doi.org/10.1182/blood-2016-10-743302

Published: 2017

Includes: Supplemental data

Journal Articles

Adaptive NK cells can persist in patients with GATA2 mutation depleted of stem and progenitor cells

Blood (2017) 129 (14): 1927–1939.

https://doi.org/10.1182/blood-2016-08-734236

Published: 2017

Includes: Supplemental data

Journal Articles

Acquired somatic mutations in PNH reveal long-term maintenance of adaptive NK cells independent of HSPCs

Marcus A. F. Corat, Heinrich Schlums, Chuanfeng Wu, Jakob Theorell, Diego A. Espinoza, Stephanie E. Sellers, Danielle M. Townsley, Neal S. Young, Yenan T. Bryceson, Cynthia E. Dunbar, Thomas Winkler

Blood (2017) 129 (14): 1940–1946.

https://doi.org/10.1182/blood-2016-08-734285

Published: 2017

Includes: Supplemental data

Journal Articles

HLH susceptibility: genetic lesions add up

Marie Meeths, Yenan T. Bryceson

Blood (2016) 127 (17): 2051–2052.

https://doi.org/10.1182/blood-2016-03-700609

Published: 2016

Journal Articles

Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3

Blood (2015) 125 (4): 639–648.

https://doi.org/10.1182/blood-2014-04-570101

Published: 2015

Includes: Supplemental data

Journal Articles

CMV Reactivation is Associated with Reduced Relapse Risk, Better Disease-Free Survival and Expansion of Adaptive NK Cells after Reduced Intensity Hematopoietic Cell Transplantation

Frank Cichocki, PhD, Zachary B. Davis, PhD, Todd E. DeFor, MS, Sarah A. Cooley, MD MS, Yenan T. Bryceson, PhD, Don J. Diamond, PhD, Bruce R. Blazar, MD, Claudio Brunstein, MD, John E. Wagner, MD, Michael R. Verneris, MD, Daniel J. Weisdorf, MD, Jeffrey S. Miller, MD

Blood (2014) 124 (21): 668.

https://doi.org/10.1182/blood.V124.21.668.668

Published: 2014

Journal Articles

Clonal Expansion of Adaptive NK Cells and NKG2C + CD57 + KIR-Expressing T Cells from Sibling, but Not Umbilical Cord Blood, Grafts Is Induced By Recipient Latent CMV and Is Associated with Protection Against CMV Reactivation

Zachary B. Davis, PhD, Frank Cichocki, PhD, Martin Felices, PhD, Rose Wangen, Todd E. DeFor, MS, Sarah A. Cooley, MD MS, Yenan T. Bryceson, PhD, Don J. Diamond, PhD, Claudio Brunstein, MD, Bruce R. Blazar, MD, John E. Wagner, MD, Daniel J. Weisdorf, MD, Amir Horowitz, Lisbeth A Guethlein, Peter Parham, PhD, Michael R. Verneris, MD, Jeffrey S. Miller, MD

Blood (2014) 124 (21): 181.

https://doi.org/10.1182/blood.V124.21.181.181

Published: 2014

Journal Articles

Surface CD107a/LAMP-1 protects natural killer cells from degranulation-associated damage

André Cohnen, Samuel C. Chiang, Ana Stojanovic, Hendrik Schmidt, Maren Claus, Paul Saftig, Ottmar Janßen, Adelheid Cerwenka, Yenan T. Bryceson, Carsten Watzl

Blood (2013) 122 (8): 1411–1418.

https://doi.org/10.1182/blood-2012-07-441832

Published: 2013

Includes: Supplemental data

Journal Articles

Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production

Blood (2013) 121 (8): 1345–1356.

https://doi.org/10.1182/blood-2012-07-442558

Published: 2013

Includes: Supplemental data

Journal Articles

Lymphocyte cytotoxicity: tug-of-war on microtubules

Stephanie M. Wood, Yenan T. Bryceson

Blood (2012) 119 (17): 3873–3875.

https://doi.org/10.1182/blood-2012-02-410381

Published: 2012

Journal Articles

A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes

Blood (2012) 119 (12): 2754–2763.

https://doi.org/10.1182/blood-2011-08-374199

Published: 2012

Includes: Supplemental data

Journal Articles

Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D

Blood (2011) 118 (22): 5783–5793.

https://doi.org/10.1182/blood-2011-07-369090

Published: 2011

Includes: Supplemental data

Journal Articles

Subtle differences in CTL cytotoxicity determine susceptibility to hemophagocytic lymphohistiocytosis in mice and humans with Chediak-Higashi syndrome

Blood (2011) 118 (17): 4620–4629.

https://doi.org/10.1182/blood-2011-05-356113

Published: 2011

Includes: Supplemental data

NARROW

Diagnostic guidelines for familial hemophagocytic lymphohistiocytosis revisited

Efficacy of T-cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosis

Comprehensive Exploration of NK Cell Education in ADCC Triggered By a Monoclonal Antibody or a Bispecific Killer Engager Molecule (BiKE)

RhoG deficiency abrogates cytotoxicity of human lymphocytes and causes hemophagocytic lymphohistiocytosis

HLH: genomics illuminates pathophysiological diversity

Single-cell dissection of monosomy 7 syndromes

Constitutional SAMD9L Mutations Cause Familial Myelodisplastic Syndrome with Monosomy 7 and Stable Revertant Mosaicism

Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms

Adaptive NK cells can persist in patients with GATA2 mutation depleted of stem and progenitor cells

Acquired somatic mutations in PNH reveal long-term maintenance of adaptive NK cells independent of HSPCs

HLH susceptibility: genetic lesions add up

Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3

CMV Reactivation is Associated with Reduced Relapse Risk, Better Disease-Free Survival and Expansion of Adaptive NK Cells after Reduced Intensity Hematopoietic Cell Transplantation

Clonal Expansion of Adaptive NK Cells and NKG2C + CD57 + KIR-Expressing T Cells from Sibling, but Not Umbilical Cord Blood, Grafts Is Induced By Recipient Latent CMV and Is Associated with Protection Against CMV Reactivation

Surface CD107a/LAMP-1 protects natural killer cells from degranulation-associated damage

Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production

Lymphocyte cytotoxicity: tug-of-war on microtubules

A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes

Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D

Subtle differences in CTL cytotoxicity determine susceptibility to hemophagocytic lymphohistiocytosis in mice and humans with Chediak-Higashi syndrome

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American Society of Hematology

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ASH Publications

American Society of Hematology

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