Publications by authors named "Inga Hofmann"

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Validation and clinical application of transactivation assays for RUNX1 variant classification.
Melanie Decker, Anupriya Agarwal, Andreas Benneche, Jane Churpek, Nicolas Duployez, Inga Hofmann

Blood Adv· June 2022

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Congenital X-linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6.
Raffaele Renella, Katelyn Gagne, Ellen Beauchamp, Jonathan Fogel, Aleksej Perlov, Inga Hofmann

Am J Hematol· January 2022

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Distinct genetic pathways define pre-malignant versus compensatory clonal hematopoiesis in Shwachman-Diamond syndrome.
Alyssa L Kennedy, Kasiani C Myers, James Bowman, Christopher J Gibson, Nicholas D Camarda, Inga Hofmann

Nat Commun· February 2021

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Diagnosis and treatment of pediatric myelodysplastic syndromes: A survey of the North American Pediatric Aplastic Anemia Consortium.
Taizo A Nakano, Bonnie W Lau, Kathryn E Dickerson, Marcin Wlodarski, Jessica Pollard, Inga Hofmann

Pediatr Blood Cancer· October 2020

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Hematopoietic Stem Cell Transplantation for Shwachman-Diamond Syndrome.
Kasiani Myers, Kyle Hebert, Joseph Antin, Farid Boulad, Lauri Burroughs, Inga Hofmann

Biol Blood Marrow Transplant· August 2020

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Comparison of Outcomes of Myeloablative Allogeneic Stem Cell Transplantation for Pediatric Patients with Bone Marrow Failure, Myelodysplastic Syndrome and Acute Myeloid Leukemia with and without Germline GATA2 Mutations.
Inga Hofmann, Serine Avagyan, Alyssa Stetson, Dongjing Guo, Hasan Al-Sayegh

Biol Blood Marrow Transplant· June 2020

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Infantile Myelofibrosis and Myeloproliferation with CDC42 Dysfunction.
Jeffrey M Verboon, Dilnar Mahmut, Ah Ram Kim, Mitsutoshi Nakamura, Nour J Abdulhay, Inga Hofmann

J Clin Immunol· May 2020

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TGFβ signaling underlies hematopoietic dysfunction and bone marrow failure in Shwachman-Diamond Syndrome.
Cailin E Joyce, Assieh Saadatpour, Melisa Ruiz-Gutierrez, Ozge Vargel Bolukbasi, Lan Jiang, Inga Hofmann

J Clin Invest· June 2019

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Downregulating Notch counteracts Kras-induced ERK activation and oxidative phosphorylation in myeloproliferative neoplasm.
Guangyao Kong, Xiaona You, Zhi Wen, Yuan-I Chang, Shuiming Qian, Inga Hofmann

Leukemia· March 2019

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Single-nucleotide human disease mutation inactivates a blood-regenerative GATA2 enhancer.
Alexandra A Soukup, Ye Zheng, Charu Mehta, Jun Wu, Peng Liu, Inga Hofmann

J Clin Invest· March 2019

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Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized mice.
Inga Hofmann, Mitchell J Geer, Timo Vögtle, Andrew Crispin, Dean R Campagna

Blood· September 2018

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Acute lymphoblastic leukemia in a patient with MonoMAC syndrome/GATA2 haploinsufficiency.
Ashley K Koegel, Inga Hofmann, Kristin Moffitt, Barbara Degar, Christine Duncan

Pediatr Blood Cancer· October 2016

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Poly(A)-specific ribonuclease (PARN) mediates 3'-end maturation of the telomerase RNA component.
Diane H Moon, Matthew Segal, Baris Boyraz, Eva Guinan, Inga Hofmann

Nat Genet· December 2015

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Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9.
Klaus Schmitz-Abe, Szymon J Ciesielski, Paul J Schmidt, Dean R Campagna, Fedik Rahimov, Inga Hofmann

Blood· December 2015

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Myeloproliferative Neoplasms in Children.
Inga Hofmann

J Hematop· September 2015

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Pediatric aplastic anemia and refractory cytopenia: A retrospective analysis assessing outcomes and histomorphologic predictors.
Craig M Forester, Sarah E Sartain, Dongjing Guo, Marian H Harris, Olga K Weinberg, Inga Hofmann

Am J Hematol· April 2015

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Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy.
Michael Y Zhang, Jane E Churpek, Siobán B Keel, Tom Walsh, Ming K Lee, Inga Hofmann

Nat Genet· February 2015

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Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity.
Michael Y Zhang, Siobán B Keel, Tom Walsh, Ming K Lee, Suleyman Gulsuner, Inga Hofmann

Haematologica· January 2015

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Induction of histiocytic sarcoma in mouse skeletal muscle.
Jianing Liu, Simone Hettmer, Michael D Milsom, Inga Hofmann, Frederic Hua

PLoS One· February 2013

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CTC1 Mutations in a patient with dyskeratosis congenita.
Rachel B Keller, Katelyn E Gagne, G Naheed Usmani, George K Asdourian, David A Williams, Inga Hofmann

Pediatr Blood Cancer· August 2012

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Hedgehog signaling is dispensable for adult murine hematopoietic stem cell function and hematopoiesis.
Inga Hofmann, Elizabeth H Stover, Dana E Cullen, Junhao Mao, Kelly J Morgan

Cell Stem Cell· June 2009

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Mutations of the hemophagocytic lymphohistiocytosis-associated gene UNC13D in a patient with systemic juvenile idiopathic arthritis.
Melissa M Hazen, Amy L Woodward, Inga Hofmann, Barbara A Degar, Alexei Grom

Arthritis Rheum· February 2008

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