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Biology and Biochemistry

D-Index
67
Citations
19616
World Ranking
8103
National Ranking
3668

Overview

Arleen D. Auerbach is affiliated with Rockefeller University in the United States. Their research primarily focuses on the fields of Biochemistry, Genetics and Molecular Biology, as well as Medicine. Within these areas, the scientist has contributed extensively to Molecular Biology, Genetics, Pathology and Forensic Medicine, Oncology, and Cancer Research.

The main topics explored by Arleen D. Auerbach include DNA Repair Mechanisms, CRISPR and Genetic Engineering, BRCA gene mutations in cancer, Genetic factors in colorectal cancer, Cancer-related Molecular Pathways, Carcinogens and Genotoxicity Assessment, and Porphyrin Metabolism and Disorders.

The following are some of their recent publications:

  • Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer, 2022, Nature
  • Distinct roles of BRCA2 in replication fork protection in response to hydroxyurea and DNA interstrand cross-links, 2020, Genes & Development
  • Association of clinical severity with FANCB variant type in Fanconi anemia, 2020, Blood
  • Fanconi Anemia Pathway Deficiency Drives Copy Number Variation in Squamous Cell Carcinomas, 2021, bioRxiv (Cold Spring Harbor Laboratory)
  • Comparison of the clinical phenotype and haematological course of siblings with Fanconi anaemia, 2020, British Journal of Haematology

Arleen D. Auerbach frequently collaborates with several coauthors, including Agata Smogorzewska, Francis P. Lach, Frank X. Donovan, Moonjung Jung, and Settara C. Chandrasekharappa.

The scientist has published multiple articles in venues such as bioRxiv (Cold Spring Harbor Laboratory), Blood, Nature, Genes & Development, and Blood Advances.

Best Publications

  • HEMATOPOIETIC RECONSTITUTION IN A PATIENT WITH FANCONI'S ANEMIA BY MEANS OF UMBILICAL-CORD BLOOD FROM AN HLA-IDENTICAL SIBLING

    Eliane Gluckman;Hal E. Broxmeyer;Arleen D. Auerbach;Henry S. Friedman

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

    David I. Kutler;Bhuvanesh Singh;Bhuvanesh Singh;Bhuvanesh Singh;Jaya Satagopan;Jaya Satagopan;Jaya Satagopan;Sat Dev Batish;Sat Dev Batish;Sat Dev Batish

  • A note on competing risks in survival data analysis

    J M Satagopan;L Ben-Porat;M Berwick;M Robson

  • Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

    Sarah Reid;Detlev Schindler;Helmut Hanenberg;Helmut Hanenberg;Karen Barker

  • Fanconi anemia and its diagnosis

    Arleen D. Auerbach

  • Hematologic Abnormalities in Fanconi Anemia: An International Fanconi Anemia Registry Study

    Anna Butturini;Robert Peter Gale;Robert Peter Gale;Robert Peter Gale;Peter C. Verlander;Peter C. Verlander;Peter C. Verlander;Barbara Adler-Brecher;Barbara Adler-Brecher;Barbara Adler-Brecher

  • The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia.

    Orna Levran;Claire Attwooll;Rashida T Henry;Kelly L Milton

  • High incidence of head and neck squamous cell carcinoma in patients with Fanconi anemia.

    David I. Kutler;Arleen D. Auerbach;Jaya Satagopan;Philip F. Giampietro

  • International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity.

    Arleen D. Auerbach;Andre Rogatko;Traute M. Schroeder-Kurth

  • Mutations of the SLX4 gene in Fanconi anemia

    Yonghwan Kim;Francis P Lach;Rohini Desetty;Helmut Hanenberg;Helmut Hanenberg

  • LEUKEMIA AND PRELEUKEMIA IN FANCONI ANEMIA PATIENTS : A REVIEW OF THE LITERATURE AND REPORT OF THE INTERNATIONAL FANCONI ANEMIA REGISTRY

    Arleen D. Auerbach;R.G. Allen

  • Bone marrow transplantation for Fanconi anemia

    E. Gluckman;A. D. Auerbach;M. M. Horowitz;K. A. Sobocinski

  • FANCI is a second monoubiquitinated member of the Fanconi anemia pathway

    Ashley E Sims;Elizabeth Spiteri;Robert J Sims;Adriana G Arita

  • Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method.

    Arleen D. Auerbach;Barbara Adler;R.S.K. Chaganti

  • Somatic mosaicism in Fanconi anemia: Evidence of genotypic reversion in lymphohematopoietic stem cells

    John J. Gregory;John E. Wagner;Peter C. Verlander;Orna Levran

  • A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination

    Anderson T. Wang;Taeho Kim;John E. Wagner;Brooke A. Conti

  • Positional cloning of the Fanconi anaemia group A gene

    Sinoula Apostolou;Scott A. Whitmore;Joanna Crawford;Gregory Lennon

  • 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

  • Unrelated donor bone marrow transplantation for the treatment of Fanconi anemia

    John E. Wagner;Mary Eapen;Margaret L. MacMillan;Richard E. Harris

  • Stem Cell Collection and Gene Transfer in Fanconi Anemia

    Patrick F Kelly;Susan Radtke;Christof von Kalle;Brenden Balcik

Frequent Co-Authors

Helmut Hanenberg
Helmut Hanenberg University of Duisburg-Essen
Agata Smogorzewska
Agata Smogorzewska Rockefeller University
Settara C. Chandrasekharappa
Settara C. Chandrasekharappa National Institutes of Health
John E. Wagner
John E. Wagner University of Minnesota
Detlev Schindler
Detlev Schindler University of Würzburg
David A. Williams
David A. Williams Boston Children's Hospital
Stella M. Davies
Stella M. Davies Cincinnati Children's Hospital Medical Center
Mauno Vihinen
Mauno Vihinen Lund University
Christopher G. Mathew
Christopher G. Mathew King's College London
David F. Callen
David F. Callen University of Adelaide

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