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Journal Articles

The Loss of ALDH9A1 Is a Significant Source of Endogenous DNA Damage Which May be Reversed By the Inhibition of Polyamine Transport System

Moonjung Jung, Isaac Ilyashov, Danielle Keahi, Tom Wiley, Sunandini Sridhar, Audrey Goldfarb, Haruna B Choijilsuren, Yeji Park, Ryan White, Raymond Noonan, Thomas S Carroll, Frank X. Donovan, Francis P. Lach, Arleen D. Auerbach, Settara C. Chandrasekharappa, Agata Smogorzewska

Blood (2021) 138 (Supplement 1): 1108.

https://doi.org/10.1182/blood-2021-149863

Published: 2021

Journal Articles

Association of clinical severity with FANCB variant type in Fanconi anemia

Moonjung Jung, Ramanagouda Ramanagoudr-Bhojappa, Sylvie van Twest, Rasim Ozgur Rosti, Vincent Murphy, Winnie Tan, Frank X. Donovan, Francis P. Lach, Danielle C. Kimble, Caroline S. Jiang, Roger Vaughan, Parinda A. Mehta, Filomena Pierri, Carlo Dufour, Arleen D. Auerbach, Andrew J. Deans, Agata Smogorzewska, Settara C. Chandrasekharappa

Blood (2020) 135 (18): 1588–1602.

https://doi.org/10.1182/blood.2019003249

Published: 2020

Includes: Supplemental data

Journal Articles

Clinical Severity Correlates with in Vitro Residual Function of FANCB Missense Variants

Moonjung Jung, MD, Ramanagouda Ramanagoudr Bhojappa, PhD, Ozgur Rosti, MD, Francis P. Lach, BS, Frank X. Donovan, PhD, Arleen D. Auerbach, PhD, Settara C. Chandrasekharappa, PhD, Agata Smogorzewska, MD PhD

Blood (2018) 132 (Supplement 1): 2588.

https://doi.org/10.1182/blood-2018-99-111320

Published: 2018

Journal Articles

Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia

Settara C. Chandrasekharappa, Francis P. Lach, Danielle C. Kimble, Aparna Kamat, Jamie K. Teer, Frank X. Donovan, Elizabeth Flynn, Shurjo K. Sen, Supawat Thongthip, Erica Sanborn, Agata Smogorzewska, Arleen D. Auerbach, Elaine A. Ostrander

Blood (2013) 121 (22): e138–e148.

https://doi.org/10.1182/blood-2012-12-474585

Published: 2013

Includes: Supplemental data

Journal Articles

Regulation of multiple DNA repair pathways by the Fanconi anemia protein SLX4

Yonghwan Kim, Gabriella S. Spitz, Uma Veturi, Francis P. Lach, Arleen D. Auerbach, Agata Smogorzewska

Blood (2013) 121 (1): 54–63.

https://doi.org/10.1182/blood-2012-07-441212

Published: 2013

Includes: Supplemental data

Journal Articles

FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway

Abdullah Mahmood Ali, Arun Pradhan, Thiyam Ramsingh Singh, Changhu Du, Jie Li, Kebola Wahengbam, Elke Grassman, Arleen D. Auerbach, Qishen Pang, Amom Ruhikanta Meetei

Blood (2012) 119 (14): 3285–3294.

https://doi.org/10.1182/blood-2011-10-385963

Published: 2012

Includes: Supplemental data

Journal Articles

Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations

Blood (2011) 117 (14): 3759–3769.

https://doi.org/10.1182/blood-2010-08-299917

Published: 2011

Includes: Supplemental data

Journal Articles

High Incidence of Hematopoietic Stem Cell Mosaicism in Fanconi Anemia.

Jakub Tolar, MD, PhD, Margaret L. MacMillan, Sat Dev Batish, Cindy Eide, Yeva Flit, Stella M. Davies, Bruce R. Blazar, Arleen D. Auerbach, John E. Wagner

Blood (2006) 108 (11): 993.

https://doi.org/10.1182/blood.V108.11.993.993

Published: 2006

Journal Articles

Unrelated donor bone marrow transplantation for the treatment of Fanconi anemia

John E. Wagner, Mary Eapen, Margaret L. MacMillan, Richard E. Harris, Ricardo Pasquini, Farid Boulad, Mei-Jie Zhang, Arleen D. Auerbach

Blood (2006) 109 (5): 2256–2262.

https://doi.org/10.1182/blood-2006-07-036657

Published: 2006

Journal Articles

Tolerability of Chemotherapy for AML or MDS in Children with Fanconi Anemia.

Parinda A. Mehta, MD, Talia Ileri, MD, Richard E. Harris, MD, David A. Williams, MD, Arleen D. Auerbach, MD, Franklin O. Smith, MD, Jun Mo, MD, Teresa Smolarek, MD, Patrick Kelly, MD, Stella M. Davies, MD

Blood (2005) 106 (11): 898.

https://doi.org/10.1182/blood.V106.11.898.898

Published: 2005

Journal Articles

Fludarabine (Flu) Based Cytoreductive Regimen and T-Cell Depleted Grafts from Unrelated or Mismatched Related Donors for the Treatment of High Risk Patients with Fanconi Anemia (FA).

Farid Boulad, MD, Arleen D. Auerbach, PhD, Nancy A. Kernan, MD, Trudy N. Small, MD, Susan E. Prockop, MD, Sonali Chaudhury, MD, Joanne Castanza, RN, Anne Casson, RN, Catherine Copeland, RN, Heidi Abendroth, RN, Nancy Collins, PhD, Richard J. O’Reilly

Blood (2004) 104 (11): 2152.

https://doi.org/10.1182/blood.V104.11.2152.2152

Published: 2004

Journal Articles

Hematopoietic Cell Transplantation in Fanconi Anemia Patients with Biallelic BRCA2 Mutations.

Margaret L. MacMillan, MD, Arleen D. Auerbach, PhD, John E. Wagner, MD

Blood (2004) 104 (11): 2838.

https://doi.org/10.1182/blood.V104.11.2838.2838

Published: 2004

Journal Articles

A Rapid Method for Retroviral Mediated Subtyping of Complementation Group in Fanconi Anemia Patients.

Saurabh Chandra, MBBS, PhD, Orna Levran, PhD, Ingrid Jurickova, MD, Chiel Mass, Rick Kapur, Helmut Hanenberg, MD, Arleen D. Auerbach, PhD, David A. Williams, MD

Blood (2004) 104 (11): 5261.

https://doi.org/10.1182/blood.V104.11.5261.5261

Published: 2004

Journal Articles

High Sensitivity and Specificity of Retroviral Complementation Group Assignment in Primary T Cells of Fanconi Anemia (FA) Patients.

Helmut Hanenberg, MD, Stephan Lobitz, MD, Indira Kokemohr, MD, Silke Furlan, BS, Orna Levran, PhD, Arleen D. Auerbach, PhD, Reinhard Kalb, PhD, Michaela Gross, PhD, Richard Friedl, BS, B. Gottwald, BS, Detlev Schindler, MD

Blood (2004) 104 (11): 3249.

https://doi.org/10.1182/blood.V104.11.3249.3249

Published: 2004

Journal Articles

Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia

John E. Wagner, Jakub Tolar, Orna Levran, Thomas Scholl, Amie Deffenbaugh, Jaya Satagopan, Leah Ben-Porat, Katherine Mah, Sat Dev Batish, David I. Kutler, Margaret L. MacMillan, Helmut Hanenberg, Arleen D. Auerbach

Blood (2004) 103 (8): 3226–3229.

https://doi.org/10.1182/blood-2003-09-3138

Published: 2004

Journal Articles

A 20-year perspective on the International Fanconi Anemia Registry (IFAR)

David I. Kutler, Bhuvanesh Singh, Jaya Satagopan, Sat Dev Batish, Marianne Berwick, Philip F. Giampietro, Helmut Hanenberg, Arleen D. Auerbach

Blood (2003) 101 (4): 1249–1256.

https://doi.org/10.1182/blood-2002-07-2170

Published: 2003

Journal Articles

Phenotypic Consequences of Mutations in the Fanconi Anemia FAC Gene: An International Fanconi Anemia Registry Study

Alfred P. Gillio, Peter C. Verlander, S.D. Batish, P.F. Giampietro, Arleen D. Auerbach

Blood (1997) 90 (1): 105–110.

https://doi.org/10.1182/blood.V90.1.105

Published: 1997

NARROW

The Loss of ALDH9A1 Is a Significant Source of Endogenous DNA Damage Which May be Reversed By the Inhibition of Polyamine Transport System

Association of clinical severity with FANCB variant type in Fanconi anemia

Clinical Severity Correlates with in Vitro Residual Function of FANCB Missense Variants

Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia

Regulation of multiple DNA repair pathways by the Fanconi anemia protein SLX4

FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway

Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations

High Incidence of Hematopoietic Stem Cell Mosaicism in Fanconi Anemia.

Unrelated donor bone marrow transplantation for the treatment of Fanconi anemia

Tolerability of Chemotherapy for AML or MDS in Children with Fanconi Anemia.

Fludarabine (Flu) Based Cytoreductive Regimen and T-Cell Depleted Grafts from Unrelated or Mismatched Related Donors for the Treatment of High Risk Patients with Fanconi Anemia (FA).

Hematopoietic Cell Transplantation in Fanconi Anemia Patients with Biallelic BRCA2 Mutations.

A Rapid Method for Retroviral Mediated Subtyping of Complementation Group in Fanconi Anemia Patients.

High Sensitivity and Specificity of Retroviral Complementation Group Assignment in Primary T Cells of Fanconi Anemia (FA) Patients.

Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia

A 20-year perspective on the International Fanconi Anemia Registry (IFAR)

Phenotypic Consequences of Mutations in the Fanconi Anemia FAC Gene: An International Fanconi Anemia Registry Study

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American Society of Hematology

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American Society of Hematology

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