Arleen D. Auerbach

15.5k citations

138 papers · 9.9k indexed · 3 hit papers · h-index 50

Impact in

Hematology top 0.2%
- Hematopoietic Stem Cell Transplantation
- Acute Myeloid Leukemia Research
Cancer Research top 0.5%
- Carcinogens and Genotoxicity Assessment

Papers in

Hematology 22
- Hematopoietic Stem Cell Transplantation 16
Molecular Biology 107
- DNA Repair Mechanisms 91
- CRISPR and Genetic Engineering 17

Co-authors: Sat Dev Batish Helmut Hanenberg David I. Kutler Jaya M. Satagopan Sandra R. Wolman Philip F. Giampietro Marianne Berwick Francis P. Lach
Journals: British Journal of Haematology (12 papers)Blood (12 papers)Human Mutation (12 papers)PEDIATRICS (5 papers)Genomics (5 papers)
Partner nations: United States Germany United Kingdom

In The Last Decade

Arleen D. Auerbach

137 papers receiving 9.6k citations

Hit Papers

align trajectories log scale

A note on competing risks in survival data analysis 2004 · 559 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2004 British Journal of Cancer
2003 Blood
1989 New England Journal of Medicine

Peers

Countries citing papers authored by Arleen D. Auerbach

Since Specialization

Citations

This map shows the geographic impact of Arleen D. Auerbach's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Arleen D. Auerbach with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Arleen D. Auerbach more than expected).

Fields of papers citing papers by Arleen D. Auerbach

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Arleen D. Auerbach. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Arleen D. Auerbach. The network helps show where Arleen D. Auerbach may publish in the future.

Co-authors

The 25 scholars most cited alongside Arleen D. Auerbach, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Arleen D. Auerbach Line = papers co-authored together Arleen D. Auerbach links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	FANCA c.3624C>T (p.Ser1208=) is a hypomorphic splice variant associated with delayed onset of Fanconi anemia Blood Advances ·雅彦樫木, Víctor Antonio Ampuero Mendoza, Francis P. Lach, Frank X. Donovan, V. Mafael, Schraner, Margaret L. MacMillan, John E. Wagner, Arleen D. Auerbach, Agata Smogorzewska, Settara C. Chandrasekharappa	2024	2
2	Association of clinical severity with FANCB variant type in Fanconi anemia Blood ·Moonjung Jung, 雅彦樫木, Sylvie van Twest, Rasim Özgür Rosti, Vincent J. Murphy, Winnie Tan, Frank X. Donovan, Francis P. Lach, Diane I. Segal, Caroline S. Jiang, Roger A. Vaughan, Parinda A. Mehta, Filomena Pierri, Carlo Dufour, Arleen D. Auerbach, Andrew J. Deans, Agata Smogorzewska, Settara C. Chandrasekharappa	2020	25
3	Distinct roles of BRCA2 in replication fork protection in response to hydroxyurea and DNA interstrand cross-links Genes & Development ·Kimberly A. Rickman, 新宇张, Francis P. Lach, Sunandini Sridhar, Anderson T. Wang, Avinash Abhyankar, Athena L. Huang, Michael C. Kelly, Arleen D. Auerbach, Agata Smogorzewska	2020	50
4	Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia Blood ·Settara C. Chandrasekharappa, Francis P. Lach, Diane I. Segal, Aparna A. Kamat, Jamie K. Teer, Frank X. Donovan, Elizabeth K. Flynn, Shurjo K. Sen, Supawat Thongthip, Erica Sanborn, Agata Smogorzewska, Arleen D. Auerbach, Elaine A. Ostrander	2013	62
5	Telomere Phenotypes in Females with Heterozygous Mutations in the Dyskeratosis Congenita 1 (DKC1) Gene Human Mutation ·Jonathan K. Alder, Erin M. Parry, Srinivasan Yegnasubramanian, Christa L. Wagner, Benjawan Intata, Robert Auerbach, Arleen D. Auerbach, Sarah J. Wheelan, Mary Armanios	2013	69
6	Correct mRNA Processing at a Mutant TT Splice Donor in FANCC Ameliorates the Clinical Phenotype in Patients and Is Enhanced by Delivery of Suppressor U1 snRNAs The American Journal of Human Genetics ·Linda Hartmann, Kornelia Neveling, 史子小畑, 上澤梨紗, Marcel Freund, Elke Grassman, Stephan Theiss, Angela Wawer, Stefan Burdach, Arleen D. Auerbach, Detlev Schindler, Helmut Hanenberg, Heiner Schaal	2010	51
7	Fanconi anemia and its diagnosis Mutation research. Fundamental and molecular mechanisms of mutagenesis ·Arleen D. Auerbach	2009	387
8	Phenotyping Genetic Diseases Using an Extension of µ-Scores for Multivariate Data Statistical Applications in Genetics and Molecular Biology ·J. Francisco Morales, Tingting Song, Arleen D. Auerbach, Knut M. Wittkowski	2008	10
9	A structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases Human Mutation ·Richard G.H. Cotton, Arleen D. Auerbach, A. F. Brown, Paola Carrera, John Christodoulou, Mireille Claustres, John G. Compton, D W Cox, Elfride De Baere, Johan T. den Dunnen, Marc S. Greenblatt, Makoto Fujiwara, Pascale Hilbert, 曹刚, Heikki Lehväslaiho, Daniel W. Nebert, Ishwar C. Verma, Mauno Vihinen	2007	9
10	Biallelic mutations in PALB2 cause Fanconi anemia and predispose to childhood cancer Cancer Research ·Sarah Reid, Detlev Schindler, Helmut Hanenberg, Marc Tischkowitz, Sandra Hanks, Karen Barker, Patrick Kelly, Sheila Seal, Sat Dev Batish, Francis P. Lach, Reinhard Kalb, Kornelia Neveling, Christopher G. Mathew, Arleen D. Auerbach, Nazneen Rahman	2007	1
11	ThePISSLREGene: Structure, Exon Skipping, and Exclusion as Tumor Suppressor in Breast Cancer Genomics ·Joanna Crawford, Leonarda Ianzano, Michelangelo Savino, S.A. Whitmore, Anne‐Marie Cleton‐Jansen, Jim Behuniak, Maria D’Apolito, R. Seshadri, Jan C. Pronk, Arleen D. Auerbach, Peter C. Verlander, Christopher G. Mathew, Alex J. Tipping, Norman A. Doggett, Chiriat'ev Ea, David F. Callen, Anna Savoia	1999	35
12	Fanconi Anemia: Genetic Testing in Ashkenazi Jews Genetic Testing ·Arleen D. Auerbach	1997	20
13	Wiskott-Aldrich syndrome in a family with Fanconi anemia The Journal of Pediatrics ·Jurg Rohrer, Raul C. Ribeiro, Arleen D. Auerbach, Jasmine Coatie, Mary Ellen Conley	1996	7
14	Umbilical cord blood transplants for genetic disease: diagnostic and ethical issues in fetal studies. PubMed ·Arleen D. Auerbach	1994	24
15	Fanconi anemia and leukemia: tracking the genes. PubMed ·Arleen D. Auerbach	1992	27
16	DNA amplification for DQ typing as an adjunct to serological prenatal HLA typing for the identification of potential donors for umbilical cord blood transplantation Human Immunology ·Marilyn S. Pollack, Arleen D. Auerbach, Hal E. Broxmeyer, Christopher T. Chen, Robert L. Griffith, (unknown)	1991	4
17	Fanconi's anaemia and pregnancy British Journal of Haematology ·Blanche P. Alter, Christine L. Frissora, Vadim Leonidovich Zemlyanskiy, Melvin H. Freedman, Usha Chitkara, 星野淳子, Lauren Lynch, Barbara Adler‐Brecher, Arleen D. Auerbach	1991	54
18	Prenatal identification of potential donors for umbilical cord blood transplantation for Fanconi anemia Transfusion ·Arleen D. Auerbach, B. A. Rodriquez, Rajat Ghosh, M S Pollack, C. J. Martínez‐Honduvilla, Hal E. Broxmeyer	1990	54
19	Announcements Annals of Hematology ·J Paul, 不老庵主人, Arleen D. Auerbach, T. M. Schroeder, Aditha Agung Prakoso, Chef pompier à New York, Hans Seidel, (unknown)	1982	1
20	A spontaneous clone of Fanconi anemia fibroblasts with chromosome abnormalities and increased growth potential Cytogenetic and Genome Research ·Arleen D. Auerbach, S R Wolman, R. S. K. Chaganti	1980	6

About Arleen D. Auerbach

Arleen D. Auerbach is a scholar working on Hematology, Molecular Biology, Genetics, Cancer Research and Pediatrics, Perinatology and Child Health, having authored 138 papers that have together received 9.9k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (91 papers), BRCA gene mutations in cancer (21 papers), Carcinogens and Genotoxicity Assessment (21 papers), Acute Lymphoblastic Leukemia research (20 papers), CRISPR and Genetic Engineering (17 papers), Hematopoietic Stem Cell Transplantation (16 papers), Prenatal Screening and Diagnostics (16 papers) and Genomic variations and chromosomal abnormalities (15 papers). The work is most often cited by research in Hematology (2.4k citations), Cancer Research (1.7k citations), Genetics (1.2k citations), Molecular Biology (6.4k citations) and Genetics (2.3k citations). Arleen D. Auerbach has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Sat Dev Batish, Helmut Hanenberg, David I. Kutler, Jaya M. Satagopan, Sandra R. Wolman, Philip F. Giampietro, Marianne Berwick, Francis P. Lach, Peter C. Verlander and Agata Smogorzewska. Their work appears in journals such as British Journal of Haematology, Blood, Human Mutation, PEDIATRICS and Genomics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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