Matthew N. Bainbridge

52.7k total citations · 2 hit papers
62 papers, 3.8k citations indexed

About

Matthew N. Bainbridge is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Matthew N. Bainbridge has authored 62 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 30 papers in Genetics and 7 papers in Genetics. Recurrent topics in Matthew N. Bainbridge's work include Genomics and Rare Diseases (17 papers), Genomic variations and chromosomal abnormalities (8 papers) and RNA and protein synthesis mechanisms (7 papers). Matthew N. Bainbridge is often cited by papers focused on Genomics and Rare Diseases (17 papers), Genomic variations and chromosomal abnormalities (8 papers) and RNA and protein synthesis mechanisms (7 papers). Matthew N. Bainbridge collaborates with scholars based in United States, Canada and Germany. Matthew N. Bainbridge's co-authors include Steven J.M. Jones, Richard Varhol, Martin Hirst, Marco A. Marra, Gordon Robertson, Richard A. Gibbs, Allen Delaney, Thomas Zeng, Misha Bilenky and Nina Thiessen and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Matthew N. Bainbridge

62 papers receiving 3.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing

2007 1.0k citations Matthew N. Bainbridge et al. profile →
Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization

2018 280 citations Lauge Farnaes, Amber Hildreth et al. npj Genomic Medicine profile →

Peers

Countries citing papers authored by Matthew N. Bainbridge

Since Specialization

Citations

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

Fields of papers citing papers by Matthew N. Bainbridge

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew N. Bainbridge. 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 Matthew N. Bainbridge. The network helps show where Matthew N. Bainbridge may publish in the future.

Co-authorship network of co-authors of Matthew N. Bainbridge

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew N. Bainbridge. A scholar is included among the top collaborators of Matthew N. Bainbridge 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 Matthew N. Bainbridge. Matthew N. Bainbridge is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Biallelic Loss of Function Variants in SENP7 Cause Immunodeficiency with Neurologic and Muscular Phenotypes 2024 ·The Journal of Pediatrics ·Erica Sanford Kobayashi, (unknown), Yael Dinur Schejter, Christine Makowski, Verena Kraus, Nanda Ramchandar, Vardiella Meiner, Isabelle Thiffault, (unknown), Julie A. Cakici, Stephen F. Kingsmore, Matias Wagner, Nikolaus Rieber, Matthew N. Bainbridge	2
2	Molecular portraits of cell cycle checkpoint kinases in cancer evolution, progression, and treatment responsiveness 2023 ·Science Advances ·(unknown), (unknown), (unknown), Aloran Mazumder, (unknown), (unknown), (unknown), (unknown), (unknown), Jonathan T. Lei, Bora Lim, Susan E. Waltz, Shreya Raghavan, Matthew N. Bainbridge, Svasti Haricharan	10
3	Reclassification of the Etiology of Infant Mortality With Whole-Genome Sequencing 2023 ·JAMA Network Open ·Mallory Owen, Meredith S. Wright, Serge Batalov, Yong-Hyun Kwon, Yan Ding, Kevin Chau, Shimul Chowdhury, Nathaly M. Sweeney, Elizabeth Kiernan, Andrew Richardson, (unknown), Rebecca J. Baer, Gretchen Bandoli, Joseph G. Gleeson, Matthew N. Bainbridge, Christina Chambers, Stephen F. Kingsmore	22
4	Clinical variants in Caenorhabditis elegans expressing human STXBP1 reveal a novel class of pathogenic variants and classify variants of uncertain significance 2023 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), Trisha Brock, (unknown), (unknown), (unknown), Christine Kim, Jennifer A. Lawson, Ingo Helbig, Matthew N. Bainbridge	4
5	NGLY1 deficiency: estimated incidence, clinical features, and genotypic spectrum from the NGLY1 Registry 2022 ·Orphanet Journal of Rare Diseases ·(unknown), Selina S. Dwight, (unknown), (unknown), (unknown), (unknown), Erica Sanford Kobayashi, Sandra Tong, Matthew N. Bainbridge	13
6	Phenotypic screening models for rapid diagnosis of genetic variants and discovery of personalized therapeutics 2022 ·Molecular Aspects of Medicine ·Christopher E. Hopkins, Trisha Brock, Thomas R. Caulfield, Matthew N. Bainbridge	8
7	Approaches to long-read sequencing in a clinical setting to improve diagnostic rate 2022 ·Scientific Reports ·Erica Sanford Kobayashi, Serge Batalov, Aaron M. Wenger, Christine Lambert, (unknown), Richard Hall, Primo Baybayan, Yan Ding, Seema Rego, Kristen Wigby, Jennifer Friedman, Charlotte A. Hobbs, Matthew N. Bainbridge	28
8	Postmortem diagnosis of PPA2-associated sudden cardiac death from dried blood spot in a neonate presenting with vocal cord paralysis 2020 ·Molecular Case Studies ·Erica Sanford Kobayashi, Marilyn C. Jones, Matthew T. Brigger, Monia Hammer, (unknown), Stephen F. Kingsmore, David Dimmock, Matthew N. Bainbridge	10
9	Determining the incidence of rare diseases 2020 ·Human Genetics ·Matthew N. Bainbridge	8
10	Comprehensive Profiling of DNA Repair Defects in Breast Cancer Identifies a Novel Class of Endocrine Therapy Resistance Drivers 2018 ·Clinical Cancer Research ·Meenakshi Anurag, (unknown), Jeremy Hoog, Matthew N. Bainbridge, Matthew J. Ellis, Svasti Haricharan	57
11	Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization breakdown → 2018 ·npj Genomic Medicine ·Lauge Farnaes, Amber Hildreth, Nathaly M. Sweeney, Michelle M. Clark, Shimul Chowdhury, Shareef Nahas, Julie A. Cakici, Wendy Benson, Robert H. Kaplan, Richard Kronick, Matthew N. Bainbridge, Jennifer Friedman, Jeffrey J. Gold, Yan Ding, Narayanan Veeraraghavan, David Dimmock, Stephen F. Kingsmore	280
12	Loss of MutL Disrupts CHK2-Dependent Cell-Cycle Control through CDK4/6 to Promote Intrinsic Endocrine Therapy Resistance in Primary Breast Cancer 2017 ·Cancer Discovery ·Svasti Haricharan, (unknown), Purba Singh, Kimberly R. Holloway, Meenakshi Anurag, (unknown), (unknown), Jonathan T. Lei, Vera J. Suman, Kelly K. Hunt, John A. Olson, Jeremy Hoog, Shunqiang Li, Shixia Huang, Dean P. Edwards, Shyam M. Kavuri, Matthew N. Bainbridge, X. Cynthia, Matthew J. Ellis	50
13	Analyses of SLC13A5 -epilepsy patients reveal perturbations of TCA cycle 2017 ·Molecular Genetics and Metabolism ·Matthew N. Bainbridge, Erin Cooney, Marcus J. Miller, Adam D. Kennedy, Jacob Wulff, Taraka Donti, Shalini N. Jhangiani, Richard A. Gibbs, Sarah H. Elsea, Brenda E. Porter, Brett H. Graham	47
14	Molecular subtyping of tumors from patients with familial glioma 2017 ·Neuro-Oncology ·(unknown), Corinne Praska, Georgina Armstrong, Thomas M. Kollmeyer, Seiji Yamada, Paul A. Decker, Matthew Kosel, Jeanette E. Eckel‐Passow, Daniel H. Lachance, Matthew N. Bainbridge, Beatrice Melin, Melissa L. Bondy, Robert B. Jenkins	7
15	Whole-exome sequencing identifies novel homozygous mutation in NPAS2 in family with nonobstructive azoospermia 2015 ·Fertility and Sterility ·Ranjith Ramasamy, Emre Bakırcıoğlu, (unknown), Ender Karaca, Jason M. Scovell, Shalini N. Jhangiani, Zeynep Coban‐Akdemir, Matthew N. Bainbridge, Yao Yu, Chad D. Huff, Richard A. Gibbs, James R. Lupski, Dolores J. Lamb	49
16	Somatic mutation load of estrogen receptor-positive breast tumors predicts overall survival: an analysis of genome sequence data 2014 ·Breast Cancer Research and Treatment ·Svasti Haricharan, Matthew N. Bainbridge, Paul Scheet, Powel H. Brown	76
17	Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1) 2013 ·Human Molecular Genetics ·(unknown), James G. Colebatch, Matthew N. Bainbridge, Steven S. Scherer, Charles K. Abrams, (unknown), Mona M. Freidin, Shalini N. Jhangiani, Mark L. Wang, Yuan Wu, D. Muzny, Robert W. Lindeman, Richard A. Gibbs	16
18	De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome 2013 ·Genome Medicine ·Matthew N. Bainbridge, Hao Hu, Donna M. Muzny, Luciana Musante, James R. Lupski, Brett H. Graham, Wei Chen, Karen W. Gripp, Kim Jenny, Thomas F. Wienker, Yaping Yang, V. Reid Sutton, Richard A. Gibbs, Hans‐Hilger Ropers	102
19	Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes 2012 ·BMC Medical Genomics ·Luca A. Lotta, Mark L. Wang, Jin Yu, Ida Martinelli, Fuli Yu, Serena M. Passamonti, Dario Consonni, Emanuela Pappalardo, Marzia Menegatti, Steven E. Scherer, Lora Lewis, (unknown), Yuanqing Wu, Matthew N. Bainbridge, Donna M. Muzny, Pier Mannuccio Mannucci, Richard A. Gibbs, Flora Peyvandi	29
20	Whole‐exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria 2011 ·American Journal of Medical Genetics Part A ·David R. Murdock, Gary Clark, Matthew N. Bainbridge, Irene Newsham, Yuanqing Wu, Donna M. Muzny, Sau Wai Cheung, Richard A. Gibbs, Melissa B. Ramocki	40

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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