Erica Sanborn

1.1k total citations
10 papers, 782 citations indexed

About

Erica Sanborn is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Erica Sanborn has authored 10 papers receiving a total of 782 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Erica Sanborn's work include DNA Repair Mechanisms (7 papers), Prenatal Screening and Diagnostics (2 papers) and Genomics and Phylogenetic Studies (2 papers). Erica Sanborn is often cited by papers focused on DNA Repair Mechanisms (7 papers), Prenatal Screening and Diagnostics (2 papers) and Genomics and Phylogenetic Studies (2 papers). Erica Sanborn collaborates with scholars based in United States and Germany. Erica Sanborn's co-authors include Agata Smogorzewska, Francis P. Lach, Arleen D. Auerbach, Stacey Gabriel, Avinash Abhyankar, Carrie Sougnez, Heather Zierhut, Jennifer A. Kennedy, Settara C. Chandrasekharappa and Frank X. Donovan and has published in prestigious journals such as Blood, Molecular Cell and Cell Reports.

In The Last Decade

Erica Sanborn

10 papers receiving 772 citations

Peers

Countries citing papers authored by Erica Sanborn

Since Specialization

Citations

This map shows the geographic impact of Erica Sanborn'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 Erica Sanborn with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Erica Sanborn more than expected).

Fields of papers citing papers by Erica Sanborn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Erica Sanborn. 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 Erica Sanborn. The network helps show where Erica Sanborn may publish in the future.

Co-authorship network of co-authors of Erica Sanborn

This figure shows the co-authorship network connecting the top 25 collaborators of Erica Sanborn. A scholar is included among the top collaborators of Erica Sanborn based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Erica Sanborn. Erica Sanborn is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	Paternal or Maternal Uniparental Disomy of Chromosome 16 Resulting in Homozygosity of a Mutant Allele Causes Fanconi Anemia 2016 ·Human Mutation ·Frank X. Donovan, (unknown), Yonghwan Kim, Francis P. Lach, Ursula L. Harper, Aparna A. Kamat, MaryPat Jones, Erica Sanborn, (unknown), John E. Wagner, Margaret L. MacMillan, Elaine A. Ostrander, Arleen D. Auerbach, Agata Smogorzewska, Settara C. Chandrasekharappa	7
2	Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia 2015 ·Cell Reports ·Kimberly A. Rickman, Francis P. Lach, Avinash Abhyankar, Frank X. Donovan, Erica Sanborn, Jennifer A. Kennedy, Carrie Sougnez, Stacey Gabriel, Olivier Elemento, Settara C. Chandrasekharappa, Detlev Schindler, Arleen D. Auerbach, Agata Smogorzewska	111
3	A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination 2015 ·Molecular Cell ·Anderson T. Wang, Tae Ho Kim, John E. Wagner, Brooke A. Conti, Francis P. Lach, Athena L. Huang, Henrik Molina, Erica Sanborn, Heather Zierhut, Belinda K. Cornes, Avinash Abhyankar, Carrie Sougnez, Stacey Gabriel, Arleen D. Auerbach, Stephen C. Kowalczykowski, Agata Smogorzewska	205
4	Natural history and management of Fanconi anemia patients with head and neck cancer: A 10‐year follow‐up 2015 ·The Laryngoscope ·David I. Kutler, Krupa R. Patel, Arleen D. Auerbach, Jennifer A. Kennedy, Francis P. Lach, Erica Sanborn, Marc A. Cohen, William I. Kuhel, Agata Smogorzewska	65
5	Disability training in the genetic counseling curricula: Bridging the gap between genetic counselors and the disability community 2014 ·American Journal of Medical Genetics Part A ·Erica Sanborn, (unknown)	16
6	Genetic Counseling for Fanconi Anemia: Crosslinking Disciplines 2014 ·Journal of Genetic Counseling ·Heather Zierhut, (unknown), Erica Sanborn	11
7	Comprehensive Analysis of Pathogenic Deletion Variants in Fanconi Anemia Genes 2014 ·Human Mutation ·Elizabeth K. Flynn, Aparna A. Kamat, Francis P. Lach, Frank X. Donovan, (unknown), Narisu Narisu, Erica Sanborn, Farid Boulad, Stella M. Davies, Alfred P. Gillio, Richard E. Harris, Margaret L. MacMillan, John E. Wagner, Agata Smogorzewska, Arleen D. Auerbach, Elaine A. Ostrander, Settara C. Chandrasekharappa	33
8	Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia 2013 ·Blood ·Settara C. Chandrasekharappa, Francis P. Lach, (unknown), 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	62
9	Double‐blind therapeutic trial in Angelman syndrome using betaine and folic acid 2010 ·American Journal of Medical Genetics Part A ·Sarika U. Peters, Lynne M. Bird, Virginia Kimonis, Daniel G. Glaze, (unknown), Terry Jo Bichell, Rene Barbieri‐Welge, Mark Nespeca, Irina Anselm, Susan E. Waisbren, Erica Sanborn, Qin Sun, William E. O’Brien, Arthur L. Beaudet, Carlos A. Bacino	32
10	An expanded version of the Hammersmith Functional Motor Scale for SMA II and III patients 2007 ·Neuromuscular Disorders ·Jessica O’Hagen, Allan M. Glanzman, Michael McDermott, Patricia Ryan, Jean Flickinger, Janet Quigley, Susan Riley, Erica Sanborn, Carrie Irvine, William B. Martens, Christine Annis, Rabi Tawil, Maryam Oskoui, Basil T. Darras, Richard S. Finkel, Darryl C. De Vivo	240

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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