K. Myers

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The clinical phenotype of children with Fanconi anemia caused by biallelic FANCD1/BRCA2 mutations

S. Spunt, T. Smolarek, A. Auerbach, 2012, Pediatric blood & cancer.

CCR5 inhibitor as novel acute graft versus host disease prophylaxis in children and young adults undergoing allogeneic stem cell transplant: results of the phase II study

K. Myers, S. Davies, P. Mehta, 2020, Bone Marrow Transplantation.

Graft rejection markers in children undergoing hematopoietic cell transplant for bone marrow failure

K. Myers, S. Davies, S. Jodele, 2021, Blood advances.

Complement blockade for TA-TMA: lessons learned from large pediatric cohort treated with eculizumab.

Ranjit S. Chima, Kana Mizuno, K. Myers, 2020, Blood.

Tryptophan metabolism is dysregulated in individuals with Fanconi anemia.

K. Myers, S. Davies, Nathan Luebbering, 2021, Blood advances.

A Reduced-Intensity Conditioning Regimen for Patients with Dyskeratosis Congenita Undergoing Hematopoietic Stem Cell Transplantation.

K. Myers, S. Davies, P. Mehta, 2016, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Somatic mutations and clonal hematopoiesis in congenital neutropenia.

Christopher A. Miller, R. Fulton, J. Baty, 2018, Blood.

Distinct genetic pathways define pre-leukemic and compensatory clonal hematopoiesis in Shwachman-Diamond syndrome

Nicholas D. Camarda, S. Carter, M. Norkin, 2020, bioRxiv.

Outcomes After Second Hematopoietic Cell Transplant for Children and Young Adults with Relapsed Acute Leukemia

Chi-kong Li, K. Myers, P. Mehta, 2019 .

Long-term survival and late effects among one-year survivors of second allogeneic hematopoietic cell transplantation for relapsed acute leukemia and myelodysplastic syndromes.

M. Norkin, W. Wood, M. Sorror, 2015, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Antibody response to human papillomavirus vaccination and natural exposure in individuals with Fanconi Anemia.

K. Myers, S. Davies, P. Mehta, 2017, Vaccine.

High-Risk Human Papillomavirus E 6 Protein Promotes Reprogramming of Fanconi Anemia Patient Cells through Repression of p 53 but Does Not Allow for Sustained Growth of Induced Pluripotent Stem Cells

Elizabeth E. Hoskins, K. Wikenheiser-Brokamp, C. Mayhew, 2014 .

High-Risk Human Papillomavirus E6 Protein Promotes Reprogramming of Fanconi Anemia Patient Cells through Repression of p53 but Does Not Allow for Sustained Growth of Induced Pluripotent Stem Cells

Elizabeth E. Hoskins, K. Wikenheiser-Brokamp, C. Mayhew, 2014, Journal of Virology.

ALLOGENEIC HEMATOPOIETIC CELL TRANSPLANTATION FOR NEUROBLASTOMA: THE CIBMTR EXPERIENCE

S. Grupp, N. Ueno, R. Gale, 2013, Bone Marrow Transplantation.

Oral Human Papillomavirus Is Common in Individuals with Fanconi Anemia

Elizabeth E. Hoskins, K. Myers, S. Davies, 2015, Cancer Epidemiology, Biomarkers & Prevention.

Diagnosis, Treatment, and Molecular Pathology of Shwachman-Diamond Syndrome.

K. Myers, A. Nelson, 2018, Hematology/oncology clinics of North America.

Late effects in hematopoietic cell transplant recipients with acquired severe aplastic anemia: a report from the late effects working committee of the center for international blood and marrow transplant research.

W. Wood, M. Sorror, M. Aljurf, 2012, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

The injured heart: early cardiac effects of hematopoietic stem cell transplantation in children and young adults

M. D. Taylor, K. Myers, S. Davies, 2017, Bone Marrow Transplantation.

Inflammatory manifestations in patients with Shwachman–Diamond syndrome: A novel phenotype

Ankoor S. Shah, T. Libermann, A. Geddis, 2020, American journal of medical genetics. Part A.

Thinking Beyond HLH: Clinical Features of Patients with Concurrent Presentation of Hemophagocytic Lymphohistiocytosis and Thrombotic Microangiopathy

K. Myers, S. Davies, S. Jodele, 2020, Journal of Clinical Immunology.

Autophagy in mesenchymal progenitors protects mice against bone marrow failure after severe intermittent stress

D. Strunk, H. Leonhardt, K. Götze, 2021, Blood.

Case Report: Cerebral Revascularization in a Child With Mucopolysaccharidosis Type I

Edward R. Smith, A. Byars, S. Vadivelu, 2021, Frontiers in Pediatrics.

Single Ultra-High-Dose Cholecalciferol to Prevent Vitamin D Deficiency in Pediatric Hematopoietic Stem Cell Transplantation.

C. Gordon, K. Myers, S. Davies, 2018, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Vitamin D Deficiency in Pediatric Hematopoietic Stem Cell Transplantation Patients Despite Both Standard and Aggressive Supplementation.

K. Myers, S. Davies, S. Jodele, 2016, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Poor Growth, Thyroid Dysfunction and Vitamin D Deficiency Remain Prevalent Despite Reduced Intensity Chemotherapy for Hematopoietic Stem Cell Transplantation in Children and Young Adults

K. Myers, S. Davies, S. Jodele, 2016, Bone Marrow Transplantation.

Vitamin D Deficiency and Survival in Children after Hematopoietic Stem Cell Transplant.

K. Setchell, K. Myers, S. Davies, 2015, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

TA-TMA risk stratification: is there a window of opportunity to improve outcomes?

Ranjit S. Chima, K. Myers, S. Jodele, 2022, Transplantation and cellular therapy.

Testicular thrombotic microangiopathy: An unrecognized complication

K. Myers, S. Davies, S. Jodele, 2021, Pediatric blood & cancer.

A pragmatic multi-institutional approach to understanding transplant-associated thrombotic microangiopathy after stem cell transplant.

Ranjit S. Chima, K. Mahadeo, K. Myers, 2020, Blood advances.

Multiple bloodstream infections in pediatric stem cell transplant recipients: A case series

K. Myers, S. Davies, S. Jodele, 2018, Pediatric blood & cancer.

A Complete Histologic Approach to Gastrointestinal Biopsy From Hematopoietic Stem Cell Transplant Patients With Evidence of Transplant-Associated Gastrointestinal Thrombotic Microangiopathy.

K. Myers, S. Jodele, C. Dandoy, 2017, Archives of pathology & laboratory medicine.

Histologic Features of Intestinal Thrombotic Microangiopathy in Pediatric and Young Adult Patients after Hematopoietic Stem Cell Transplantation.

K. Myers, S. Davies, S. Jodele, 2015, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Xenon-129 MRI detects ventilation deficits in paediatric stem cell transplant patients unable to perform spirometry

K. Myers, S. Davies, J. Woods, 2019, European Respiratory Journal.

Understanding the evolving phenotype of vascular complications in telomere biology disorders

Anne R. Pariser, G. Raghu, F. Johnson, 2018, Angiogenesis.

Pericardial effusion requiring surgical intervention after stem cell transplantation: a case series

Ranjit S. Chima, K. Myers, S. Davies, 2017, Bone Marrow Transplantation.

Terminal Complement Blockade after Hematopoietic Stem Cell Transplantation Is Safe without Meningococcal Vaccination.

K. Myers, S. Davies, S. Jodele, 2016, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

A Prospective Study of Alemtuzumab as a Second-Line Agent for Steroid-Refractory Acute Graft-versus-Host Disease in Pediatric and Young Adult Allogeneic Hematopoietic Stem Cell Transplantation.

A. Vinks, K. Myers, S. Davies, 2016, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

The successful use of alemtuzumab for treatment of steroid‐refractory acute graft‐versus‐host disease in pediatric patients

K. Myers, S. Davies, P. Mehta, 2014, Pediatric transplantation.

Myelodysplastic syndrome and acute myeloid leukemia in patients with Shwachman Diamond syndrome: a multicentre, retrospective, cohort study

K. Myers, F. Boulad, Elissa Furutani, 2021 .

Clinical features and outcomes of patients with Shwachman-Diamond syndrome and myelodysplastic syndrome or acute myeloid leukaemia: a multicentre, retrospective, cohort study.

M. Norkin, M. Oberley, M. Fleming, 2019, The Lancet. Haematology.

Impaired immune function in children and adults with Fanconi anemia

K. Myers, S. Davies, P. Mehta, 2017, Pediatric blood & cancer.

Rapid rituximab infusion is safe in paediatric and young adult patients with non‐malignant indications

K. Myers, S. Davies, S. Jodele, 2016, British journal of haematology.

Gastrointestinal Hemorrhage: A Manifestation of the Telomere Biology Disorders.

S. Savage, Suneet Agarwal, A. Bertuch, 2020, The Journal of pediatrics.

Mouse models of neutropenia reveal progenitor-stage-specific defects

David E. Muench, Kristopher L. Nazor, N. Salomonis, 2020, Nature.

Ruxolitinib as Salvage Therapy in Steroid-Refractory Acute Graft-versus-Host Disease in Pediatric Hematopoietic Stem Cell Transplant Patients.

K. Myers, S. Davies, S. Jodele, 2017, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Pain, depressive symptoms, and health‐related quality of life among survivors of pediatric hematopoietic stem cell transplant

Caroline F. Morrison, K. Myers, A. Pai, 2022, Pediatric blood & cancer.

Topical vitamin D analog for chronic graft versus host disease of the skin

K. Myers, S. Davies, S. Jodele, 2018, Bone Marrow Transplantation.

Prospective pilot trial of calcipotriene as a novel topical treatment for acute skin graft versus host disease

K. Myers, S. Davies, S. Jodele, 2021, Bone Marrow Transplantation.

Combination of High-Dose Methylprednisolone and Defibrotide for Veno-Occlusive Disease in Pediatric Hematopoietic Stem Cell Transplant Recipients.

K. Myers, S. Davies, S. Jodele, 2017, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Symptoms of Survivors of Pediatric Hematopoietic Stem Cell Transplant by Age, Sex, and Transplant Type

Caroline F. Morrison, K. Myers, A. Pai, 2022, Journal of pediatric hematology/oncology nursing.

Second Allogeneic Hematopoietic Cell Transplantation for Patients with Fanconi Anemia and Bone Marrow Failure.

H. Deeg, J. Wagner, R. Gale, 2015, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

High-dose methylprednisolone for veno-occlusive disease of the liver in pediatric hematopoietic stem cell transplantation recipients.

K. Myers, S. Davies, S. Jodele, 2013, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Veno-occlusive disease of the liver in the absence of elevation in bilirubin in pediatric patients after hematopoietic stem cell transplantation.

K. Myers, S. Davies, S. Jodele, 2015, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Endocrine phenotype of children and adults with Fanconi anemia

J. Khoury, K. Myers, S. Davies, 2012, Pediatric blood & cancer.

Successful use of a therapeutic trial of graduated volume and dose escalation for postoperative head and neck radiotherapy in a Fanconi anemia patient

J. Greenberger, V. Takiar, K. Myers, 2020, Head & neck.

Bone Health Outcomes at One Year After HSCT in a Heterogeneous Pediatric Population.

K. Myers, J. Howell, Anthony Sabulski, 2021, Transplantation and cellular therapy.

Overcoming Pluripotent Stem Cell Dependence on the Repair of Endogenous DNA Damage

K. Wikenheiser-Brokamp, C. Mayhew, J. Wells, 2016, Stem cell reports.

Chemotherapy-Only Preparative Regimen for Alternative Donor Hematopoietic Cell Transplantation for Patients with Fanconi Anemia (FA): Results of a Multi-Institutional Study

David A. Williams, E. Guinan, K. Myers, 2015 .

Reduced Fertility Potential in Young Patients Following Hematopoietic Stem Cell Transplantation Despite Reduced Intensity Conditioning

K. Myers, S. Davies, S. Jodele, 2018 .

Kahn JM, Brazauskas R, Tecca HR, et al. Subsequent neoplasms and late mortality in children undergoing allogeneic transplantation for nonmalignant diseases. Blood Adv. 2020;4(9):2084-2094.

M. Norkin, B. George, R. Gale, 2020, Blood advances.

Reduced Intensity Conditioning Mitigates Risk for Primary Ovarian Insufficiency but Does Not Decrease Risk for Infertility in Pediatric and Young Adult Survivors of Hematopoietic Stem Cell Transplant: Gonadal Toxicity and Fertility Following Pediatric HSCT.

K. Myers, S. Jodele, C. Dandoy, 2022, Transplantation and cellular therapy.

TGFb signaling underlies hematopoietic dysfunction and bone marrow failure in Shwachman-Diamond Syndrome

C. Nusbaum, T. Libermann, Guocheng Yuan, 2019 .

TGF b signaling underlies hematopoietic dysfunction and bone marrow failure in Shwachman-Diamond Syndrome

C. Nusbaum, T. Libermann, Guocheng Yuan, 2019 .

Dyskeratosis congenita caused by a novel TERT point mutation in siblings with pancytopenia and exudative retinopathy

J. D'Orazio, K. Myers, Zhan Ye, 2014, Pediatric blood & cancer.

Quality Improvement in Hematopoietic Stem Cell Transplant and Cellular Therapy: Using the Model for Improvement to impact Outcomes.

Mark A Mueller, K. Myers, John Huber, 2022, Transplantation and cellular therapy.

Pulmonary Complications After Pediatric Stem Cell Transplant

Maya Dewan, K. Myers, C. Dandoy, 2021, Frontiers in Oncology.

Secondary Impact of the Coronavirus Disease 19 Pandemic on Patients and the Cellular Therapy Healthcare Ecosystem

David M. Hartley, D. Hartley, K. Myers, 2022, Transplantation and Cellular Therapy.

Pathogenesis of ELANE-mutant severe neutropenia revealed by induced pluripotent stem cells.

Patrick J. Paddison, B. Aronow, P. Paddison, 2015, The Journal of clinical investigation.

Second solid cancers after allogeneic hematopoietic cell transplantation using reduced-intensity conditioning.

M. Sorror, J. Wingard, U. Popat, 2014, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Clinical and molecular pathophysiology of Shwachman-Diamond syndrome: an update.

A. Shimamura, K. Myers, S. Davies, 2013, Hematology/oncology clinics of North America.

Distinct genetic pathways define pre-malignant versus compensatory clonal hematopoiesis in Shwachman-Diamond syndrome

Nicholas D. Camarda, S. Carter, M. Norkin, 2021, Nature Communications.

TGFβ signaling underlies hematopoietic dysfunction and bone marrow failure in Shwachman-Diamond Syndrome.

C. Nusbaum, T. Libermann, Guocheng Yuan, 2019, The Journal of clinical investigation.

Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond–like features

Magalie S Leduc, M. Konantz, C. Lengerke, 2017, The Journal of clinical investigation.

Variable clinical presentation of Shwachman-Diamond syndrome: update from the North American Shwachman-Diamond Syndrome Registry.

A. Shimamura, K. Myers, S. Davies, 2014, The Journal of pediatrics.

Hematopoietic stem cell transplantation for bone marrow failure syndromes in children.

K. Myers, S. Davies, 2009, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Ruxolitinib for the Treatment of Chronic GVHD and Overlap Syndrome in Children and Young Adults

K. Myers, S. Davies, P. Mehta, 2021, Transplantation.

High-dose Carboplatin/Etoposide/Melphalan increases risk of thrombotic microangiopathy and organ injury after autologous stem cell transplantation in patients with neuroblastoma

K. Myers, S. Davies, S. Jodele, 2018, Bone Marrow Transplantation.

On-chip recapitulation of clinical bone marrow toxicities and patient-specific pathophysiology

Carlos F. Ng, D. Ingber, Cailin E. Joyce, 2020, Nature Biomedical Engineering.

Variable Eculizumab Clearance Requires Pharmacodynamic Monitoring to Optimize Therapy for Thrombotic Microangiopathy after Hematopoietic Stem Cell Transplantation.

Ranjit S. Chima, B. Dixon, A. Vinks, 2016, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

The FA pathway counteracts oxidative stress through selective protection of antioxidant defense gene promoters.

P. Andreassen, W. Du, K. Myers, 2012, Blood.

Radiation-free, alternative-donor HCT for Fanconi anemia patients: results from a prospective multi-institutional study.

David A. Williams, E. Guinan, K. Myers, 2017, Blood.

Hematologic complications with age in Shwachman-Diamond syndrome

Sarah K. Steltz, A. Bertuch, A. Geddis, 2021, Blood advances.

Pneumatosis intestinalis after hematopoietic stem cell transplantation: When not doing anything is good enough.

K. Myers, S. Davies, A. Towbin, 2021, Journal of pediatric surgery.

Author Correction: On-chip recapitulation of clinical bone marrow toxicities and patient-specific pathophysiology

Carlos F. Ng, D. Ingber, Cailin E. Joyce, 2020, Nature Biomedical Engineering.

An intermediate alemtuzumab schedule reduces the incidence of mixed chimerism following reduced-intensity conditioning hematopoietic cell transplantation for hemophagocytic lymphohistiocytosis.

K. Myers, S. Davies, P. Mehta, 2013, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Survival Trends in Infants Undergoing Allogeneic Hematopoietic Cell Transplant

M. Pasquini, B. George, R. Gale, 2019, JAMA pediatrics.

Human Papillomavirus Oral- and Sero- Positivity in Fanconi Anemia

K. Myers, S. Davies, P. Mehta, 2021, Cancers.

Deletion of Fanca or Fancd2 dysregulates Treg in mice.

W. Du, K. Myers, S. Davies, 2014, Blood.

Diagnostic and risk criteria for HSCT-associated thrombotic microangiopathy: a study in children and young adults.

Ranjit S. Chima, J. Khoury, K. Myers, 2014, Blood.

Healthcare Burden, Risk Factors, and Outcomes of Mucosal Barrier Injury Laboratory-Confirmed Bloodstream Infections after Stem Cell Transplantation.

K. Myers, S. Davies, S. Jodele, 2016, Biology of Blood and Marrow Transplantation.

New approaches in the diagnosis, pathophysiology, and treatment of pediatric hematopoietic stem cell transplantation-associated thrombotic microangiopathy.

K. Myers, S. Jodele, C. Dandoy, 2016, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

The genetic fingerprint of susceptibility for transplant-associated thrombotic microangiopathy.

F. Zou, M. Medvedovic, J. Meller, 2015, Blood.

A new paradigm: Diagnosis and management of HSCT-associated thrombotic microangiopathy as multi-system endothelial injury.

B. Dixon, K. Myers, S. Davies, 2015, Blood reviews.

Variable Clinical Presentation of Shwachman-Diamond Syndrome: Update From the North-American Shwachman-Diamond Syndrome Registry.

Nicholas J. Dobbins, A. Shimamura, K. Myers, 2012 .

Pediatric myelofibrosis due to compound heterozygous MPIG6B mutations in a patient of European ancestry

R. Arora, K. Myers, R. Lorsbach, 2022, Pediatric blood & cancer.

Risk of Human Papillomavirus Infection in Cancer-Prone Individuals: What We Know

K. Myers, S. Davies, P. Mehta, 2018, Viruses.

Impaired immune function in children with Fanconi anaemia

K. Myers, S. Davies, Richard E. Harris, 2011, British journal of haematology.

Numerical chromosomal changes and risk of development of myelodysplastic syndrome--acute myeloid leukemia in patients with Fanconi anemia.

T. Smolarek, K. Myers, S. Davies, 2010, Cancer genetics and cytogenetics.

Phenotypes of adults with Fanconi anaemia.

K. Myers, S. Davies, P. Mehta, 2022, British journal of haematology.

Long-term Survival and Late Effects among 1-year Survivors of Second Allogeneic Hematopoietic Cell Transplantation for Relapsed Acute Leukemia and Myelodysplastic Syndromes

Zhiwei, Saber, M. Norkin, 2014 .

Acute myeloid leukemia in SRP54‐mutated congenital neutropenia

K. Myers, S. Davies, Anthony Sabulski, 2022, EJHaem.

The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations

Abdul Waheed Khan, F. Acquati, A. Shimamura, 2021, Molecular cytogenetics.

Repolarization of HSC attenuates HSCs failure in Shwachman–Diamond syndrome

U. Bissels, A. Bosio, A. Shimamura, 2020, Leukemia.

Experience with Alemtuzumab, Fludarabine, and Melphalan Reduced-Intensity Conditioning Hematopoietic Cell Transplantation in Patients with Nonmalignant Diseases Reveals Good Outcomes and That the Risk of Mixed Chimerism Depends on Underlying Disease, Stem Cell Source, and Alemtuzumab Regimen.

K. Myers, S. Davies, P. Mehta, 2015, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Endocrine evaluation of children with and without Shwachman-Bodian-Diamond syndrome gene mutations and Shwachman-Diamond syndrome.

J. Khoury, K. Myers, Richard E. Harris, 2013, The Journal of pediatrics.

Outcomes in Hematopoietic Stem Cell Transplantation for Congenital Amegakaryocytic Thrombocytopenia.

T. Olson, M. Aljurf, K. Myers, 2021, Transplantation and cellular therapy.

Therapeutic discovery for marrow failure with MDS predisposition using pluripotent stem cells.

K. Stegmaier, G. Alexe, D. Russell, 2019, JCI insight.

Early career mentoring through the American Society of Pediatric Hematology/Oncology: Lessons learned from a pilot program

K. Myers, S. Badawy, J. Hilden, 2017, Pediatric blood & cancer.

Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency

J. Christodoulou, H. Venselaar, R. Wevers, 2021, Genetics in Medicine.

Inherited DNA Repair Defects Disrupt the Structure and Function of Human Skin.

K. Komurov, D. Supp, D. Witte, 2020, Cell stem cell.

α4β7 Integrin expression and blockade in pediatric and young adult gastrointestinal graft‐versus‐host disease

K. Myers, S. Davies, P. Mehta, 2021, Pediatric blood & cancer.

Abnormal echocardiography 7 days after stem cell transplantation may be an early indicator of thrombotic microangiopathy.

Ranjit S. Chima, K. Myers, S. Davies, 2015, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Clinical Utility of Computed Tomography and Magnetic Resonance Imaging for Diagnosis of Posterior Reversible Encephalopathy Syndrome after Stem Cell Transplantation in Children and Adolescents.

Ranjit S. Chima, H. Wong, K. Myers, 2015, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Outcomes after bloodstream infection in hospitalized pediatric hematology/oncology and stem cell transplant patients

K. Myers, R. Nagarajan, C. Dandoy, 2019, Pediatric blood & cancer.

Personalized Prognostic Risk Score for Long-Term Survival for Children with Acute Leukemia after Allogeneic Transplantation.

V. Brown, K. Myers, S. Davies, 2017, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Risk Factors for Subsequent Central Nervous System Tumors in Pediatric Allogeneic Hematopoietic Cell Transplant: A Study from the Center for International Blood and Marrow Transplant Research (CIBMTR).

H. Sengeløv, Chi-kong Li, B. Shaw, 2017, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Outcomes of pediatric patients with therapy-related myeloid neoplasms

Cheng Cheng, K. Somers, P. Amrolia, 2021, Bone Marrow Transplantation.

Prevalence of Viral Infections in Children Undergoing First Allogenic Hematopoietic Stem Cell Transplantation: Two Year Single Center Experience

K. Myers, S. Davies, P. Mehta, 2012 .

Incidence of thyroid dysfunction in children after HSCT with reduced intensity conditioning (RIC) or myeloablative conditioning (MAC)

K. Myers, S. Davies, J. Howell, 2021, Pediatric transplantation.

Quantitative inspiratory–expiratory chest CT to evaluate pulmonary involvement in pediatric hematopoietic stem‐cell transplantation patients

A. Aliverti, K. Myers, J. Woods, 2020, Pediatric pulmonology.

On-chip recapitulation of clinical bone-marrow toxicities and patient-specific pathophysiology

Carlos F. Ng, D. Ingber, Cailin E. Joyce, 2019, Nature Biomedical Engineering.

Human bone marrow disorders recapitulated in vitro using organ chip technology

Carlos F. Ng, D. Ingber, Cailin E. Joyce, 2018, bioRxiv.

Hematopoietic Stem Cell Transplant for Shwachman Diamond Syndrome.

M. MacMillan, K. Myers, M. Eapen, 2020, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

RSV infection without ribavirin treatment in pediatric hematopoietic stem cell transplantation

K. Myers, S. Davies, S. Jodele, 2016, Bone Marrow Transplantation.

Outcomes after Second Hematopoietic Cell Transplantation in Children and Young Adults with Relapsed Acute Leukemia.

V. Brown, Chi-kong Li, K. Myers, 2019, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Complement Blockade for TA-TMA: Lessons Learned from Large Pediatric Cohort Treated with Eculizumab

Kana Mizuno, K. Myers, S. Davies, 2020 .

Eculizumab Treatment Improves Survival in Patients with High-Risk Hematopoietic Stem Cell Transplant (HSCT)-Associated Thrombotic Microangiopathy (TMA)

A. Vinks, Kana Mizuno, K. Myers, 2015 .

Team‐based approach to identify cardiac toxicity in critically ill hematopoietic stem cell transplant recipients

Ranjit S. Chima, K. Myers, S. Davies, 2017, Pediatric blood & cancer.

Abnormal circumferential strain measured by echocardiography is present in patients with Shwachman–Diamond syndrome despite normal shortening fraction

A. Shimamura, K. Myers, S. Davies, 2015, Pediatric Blood & Cancer.

protection of antioxidant defense gene promoters

P. Andreassen, W. Du, K. Myers, 2017 .

Pulmonary hypertension associated with bronchiolitis obliterans after hematopoietic stem cell transplantation

Ranjit S. Chima, K. Myers, S. Davies, 2016, Bone Marrow Transplantation.

Treatment exposures stratify need for echocardiographic screening in asymptomatic long-term survivors of hematopoietic stem cell transplantation

K. Myers, S. Davies, A. Powell, 2019, Cardiology in the Young.

Severe ocular graft versus host disease (GVHD): association with mortality in allogeneic bone marrow transplant (BMT) patients with severe systemic GVHD

Kelly E. Lusk, T. Schwartz, K. Myers, 2014 .

Pediatric and Young Adult Vulvovaginal Graft-versus-Host Disease.

K. Myers, C. Dandoy, Jeremy D. Rubinstein, 2019, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Pediatric 129Xe Gas‐Transfer MRI—Feasibility and Applicability

K. Myers, J. Woods, L. Walkup, 2022, Journal of magnetic resonance imaging : JMRI.

Effect of Autograft CD34+ Dose on Outcome in Pediatric Patients Undergoing Autologous Hematopoietic Stem Cell Transplant for Central Nervous System Tumors.

K. Myers, M. Qayed, G. Yanik, 2022, Transplantation and cellular therapy.

Understanding the evolving phenotype of vascular complications in telomere biology disorders

G. Raghu, F. Johnson, Y. Crow, 2018, Angiogenesis.

Pediatric Phase II Study of Maraviroc for Acute Graft Versus Host Disease Prophylaxis

A. Vinks, K. Myers, S. Davies, 2019, Biology of Blood and Marrow Transplantation.

Coronavirus disease 2019 and vaccination in patients with Shwachman‐Diamond syndrome

A. Shimamura, K. Myers, M. Malsch, 2022, Pediatric Blood & Cancer.

Critical Illness Risk and Long-Term Outcomes Following Intensive Care in Pediatric Hematopoietic Cell Transplant Recipients

M. Sorror, O. Ringdén, K. Myers, 2023, medRxiv.

A prospective pilot study of a novel alemtuzumab target concentration intervention strategy

A. Vinks, K. Myers, S. Davies, 2021, Bone Marrow Transplantation.

Successful management of concurrent acquired hemophilia A and a lupus anticoagulant in a pediatric hematopoietic stem cell transplant patient

K. Myers, C. Quinn, S. Jodele, 2018, Bone Marrow Transplantation.

Azithromycin does not increase hematologic relapse in pediatric hematopoietic cell transplant recipients

K. Myers, Anthony Sabulski, Stella M. Davies, 2022, Bone Marrow Transplantation.

Increased Body Mass Index Augments Endothelial Injury and Clinical Outcomes after Hematopoietic Stem Cell Transplantation

K. Myers, A. Ziady, S. Jodele, 2023, Transplantation and cellular therapy.

The clinical phenotype of children with Fanconi anemia caused by biallelic FANCD1/BRCA2 mutations

S. Spunt, T. Smolarek, A. Auerbach, 2012, Pediatric blood & cancer.

Optimized vitamin D repletion with oral thin film cholecalciferol in patients undergoing stem cell transplant

K. Myers, S. Jodele, Stella M. Davies, 2023, Blood advances.

Liver abnormalities are frequent and persistent in patients with Fanconi anemia

K. Myers, P. Mehta, A. Lane, 2024, Blood advances.

Broad de-regulated U2AF1 splicing is prognostic and augments leukemic transformation via protein arginine methyltransferase activation

M. Weirauch, K. Pradhan, N. Salomonis, 2024, bioRxiv.

Subsequent neoplasms and late mortality in children undergoing Subsequent neoplasms and late mortality in children undergoing allogeneic transplantation for nonmalignant diseases allogeneic transplantation for nonmalignant diseases

M. Norkin, B. Alter, M. Flowers, 2022 .

Ruxolitinib as Salvage Therapy in Steroid-Refractory Acute Graft-versus-Host Disease in Pediatric Hematopoietic Stem Cell Transplant Patients.

K. Myers, S. Davies, S. Jodele, 2017, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Treatment of relapsed/refractory severe aplastic anemia in children: Evidence‐based recommendations

A. Geddis, K. Myers, K. Shimano, 2024, Pediatric blood & cancer.

Treatment of newly diagnosed severe aplastic anemia in children: Evidence‐based recommendations

A. Geddis, K. Myers, K. Shimano, 2024, Pediatric blood & cancer.

Radiation-free, alternative-donor HCT for Fanconi anemia patients: results from a prospective multi-institutional study.

David A. Williams, E. Guinan, K. Myers, 2017, Blood.

The genetic fingerprint of susceptibility for transplant-associated thrombotic microangiopathy.

F. Zou, M. Medvedovic, J. Meller, 2016, Blood.

Posttransplant complications in patients with marrow failure syndromes: are we improving long-term outcomes?

K. Myers, Zahra Hudda, 2023, Hematology. American Society of Hematology. Education Program.