Publications by authors named "Roberta Parrott"

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Outcomes Following Matched Sibling Donor Transplantation for Severe Combined Immunodeficiency: A Report from the PIDTC.
Ahmad Rayes, Brent R Logan, Xuerong Liu, Jasmeen Dara, Rebecca H Buckley, Roberta Essom Parrott

Blood Adv· November 2025

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Mesenchymal stromal cells suppress microglial activation and tumor necrosis factor production.
Li Xu, Hyunjung Min, Arjun Saha, Aruni Gunaratne, Jonathan Schwartzman, Roberta Parrott

Cytotherapy· February 2024

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Posttransplantation late complications increase over time for patients with SCID: A Primary Immune Deficiency Treatment Consortium (PIDTC) landmark study.
Hesham Eissa, Monica S Thakar, Ami J Shah, Brent R Logan, Linda M Griffith, Roberta E Parrott

J Allergy Clin Immunol· January 2024

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Measuring the effect of newborn screening on survival after haematopoietic cell transplantation for severe combined immunodeficiency: a 36-year longitudinal study from the Primary Immune Deficiency Treatment Consortium.
Monica S Thakar, Brent R Logan, Jennifer M Puck, Elizabeth A Dunn, Rebecca H Buckley, Roberta E Parrott

Lancet· July 2023

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Aberrant T-cell exhaustion in severe combined immunodeficiency survivors with poor T-cell reconstitution after transplantation.
Roxane Labrosse, Ines Boufaied, Benoîte Bourdin, Saideep Gona, Haley E Randolph, Roberta E Parrott

J Allergy Clin Immunol· January 2023

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Outcomes following treatment for ADA-deficient severe combined immunodeficiency: a report from the PIDTC.
Geoffrey D E Cuvelier, Brent R Logan, Susan E Prockop, Rebecca H Buckley, Caroline Y Kuo, Roberta E Parrott

Blood· August 2022

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Cord Blood Connect: The International Congress for Cord Blood and Perinatal Tissue Research 2021.
Hyunjung Min, Li Xu, Roberta Parrott, Sebastian Wellford, Ashley Moseman

Stem Cells Transl Med· September 2021

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Autologous Ex Vivo Lentiviral Gene Therapy for Adenosine Deaminase Deficiency.
Donald B Kohn, Claire Booth, Kit L Shaw, Jinhua Xu-Bayford, Elizabeth Garabedian, Roberta Parrott

N Engl J Med· May 2021

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Mesenchymal stromal cells reprogram monocytes and macrophages with processing bodies.
Hyunjung Min, Li Xu, Roberta Parrott, Christopher C Overall, Melina Lillich

Stem Cells· January 2021

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Cord Blood Connect: The International Congress for Cord Blood and Perinatal Tissue Research 2020.
Hyunjung Min, Li Xu, Roberta Parrott, Christopher Overall, Melina Lillich

Stem Cells Transl Med· September 2020

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SCID genotype and 6-month posttransplant CD4 count predict survival and immune recovery.
Elie Haddad, Brent R Logan, Linda M Griffith, Rebecca H Buckley, Roberta E Parrott

Blood· October 2018

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B-cell differentiation and IL-21 response in SCID patients after hematopoietic stem cell transplantation.
Alexandra M Miggelbrink, Brent R Logan, Rebecca H Buckley, Roberta E Parrott, Christopher C Dvorak

Blood· June 2018

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Dominant Splice Site Mutations in PIK3R1 Cause Hyper IgM Syndrome, Lymphadenopathy and Short Stature.
Slavé Petrovski, Roberta E Parrott, Joseph L Roberts, Hongxiang Huang, Jialong Yang

J Clin Immunol· July 2016

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Clinical application of whole-genome sequencing in patients with primary immunodeficiency.
Talal Mousallem, Thomas J Urban, K Melodi McSweeney, Sarah E Kleinstein, Mingfu Zhu, Roberta E Parrott

J Allergy Clin Immunol· August 2015

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Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections.
Kerry Dobbs, Cecilia Domínguez Conde, Shen-Ying Zhang, Silvia Parolini, Magali Audry, Roberta E Parrott

N Engl J Med· June 2015

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A nonsense mutation in IKBKB causes combined immunodeficiency.
Talal Mousallem, Jialong Yang, Thomas J Urban, Hongxia Wang, Mehdi Adeli, Roberta E Parrott

Blood· September 2014

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Transplantation outcomes for severe combined immunodeficiency, 2000-2009.
Sung-Yun Pai, Brent R Logan, Linda M Griffith, Rebecca H Buckley, Roberta E Parrott

N Engl J Med· July 2014

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Post-transplantation B cell function in different molecular types of SCID.
Rebecca H Buckley, Chan M Win, Barry K Moser, Roberta E Parrott, Elisa Sajaroff

J Clin Immunol· January 2013

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CD45-deficient severe combined immunodeficiency caused by uniparental disomy.
Joseph L Roberts, Rebecca H Buckley, Biao Luo, Jianming Pei, Alla Lapidus, Roberta E Parrott

Proc Natl Acad Sci U S A· June 2012

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Thymic output, T-cell diversity, and T-cell function in long-term human SCID chimeras.
Marcella Sarzotti-Kelsoe, Chan M Win, Roberta E Parrott, Myriah Cooney, Barry K Moser

Blood· August 2009

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Unusual clinical and immunologic manifestations of transplacentally acquired maternal T cells in severe combined immunodeficiency.
Kricia Palmer, Todd D Green, Joseph L Roberts, Elisa Sajaroff, Myriah Cooney, Roberta Parrott

J Allergy Clin Immunol· August 2007

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T-B+NK+ severe combined immunodeficiency caused by complete deficiency of the CD3zeta subunit of the T-cell antigen receptor complex.
Joseph L Roberts, Jens Peter H Lauritsen, Myriah Cooney, Roberta E Parrott, Elisa O Sajaroff

Blood· April 2007

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T cell repertoire development in humans with SCID after nonablative allogeneic marrow transplantation.
Marcella Sarzotti, Dhavalkumar D Patel, Xiaojing Li, Daniel A Ozaki, Shui Cao, Roberta E Parrott

J Immunol· March 2003

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