Ming K. Lee

17.3k total citations · 4 hit papers
60 papers, 8.7k citations indexed

About

Ming K. Lee is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Ming K. Lee has authored 60 papers receiving a total of 8.7k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 30 papers in Genetics and 17 papers in Cancer Research. Recurrent topics in Ming K. Lee's work include BRCA gene mutations in cancer (25 papers), Cancer Genomics and Diagnostics (15 papers) and DNA Repair Mechanisms (10 papers). Ming K. Lee is often cited by papers focused on BRCA gene mutations in cancer (25 papers), Cancer Genomics and Diagnostics (15 papers) and DNA Repair Mechanisms (10 papers). Ming K. Lee collaborates with scholars based in United States, Israel and Palestinian Territory. Ming K. Lee's co-authors include Mary‐Claire King, Tom Walsh, Beth Newman, Lee Anderson, Bing Huey, Jeff Hall, Silvia Casadei, Elizabeth M. Swisher, Anne Thornton and Barbara M. Norquist and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and JAMA.

In The Last Decade

Ming K. Lee

58 papers receiving 8.5k 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.

Linkage of Early-Onset Familial Breast Cancer to Chromosome 17q21

1990 1.8k citations Ming K. Lee, Mary‐Claire King et al. profile →
Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas

2013 712 citations Kathryn P. Pennington, Tom Walsh et al. Clinical Cancer Research profile →
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

2011 662 citations Tom Walsh, Silvia Casadei et al. Proceedings of the National Academy of Sciences profile →
Inherited Mutations in Women With Ovarian Carcinoma

2015 503 citations Barbara M. Norquist, Maria I. Harrell et al. profile →

Peers

Countries citing papers authored by Ming K. Lee

Since Specialization

Citations

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

Fields of papers citing papers by Ming K. Lee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ming K. Lee. 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 Ming K. Lee. The network helps show where Ming K. Lee may publish in the future.

Co-authorship network of co-authors of Ming K. Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Ming K. Lee. A scholar is included among the top collaborators of Ming K. Lee 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 Ming K. Lee. Ming K. Lee 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	TP53 missense allele predisposing to high risk of breast cancer but not pediatric cancers 2024 ·JNCI Journal of the National Cancer Institute ·(unknown), Sari Lieberman, (unknown), (unknown), Ming K. Lee, Süleyman Gülsüner, (unknown), Rachel Beeri, Amal Abu Rayyan, Jessica B. Mandell, Hila Fridman, (unknown), (unknown), (unknown), Amnon Lahad, Mary‐Claire King, Ephrat Levy‐Lahad, Moien Kanaan	0
2	A paradoxical genotype-phenotype relationship: Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss 2023 ·Human Molecular Genetics ·Amal Abu Rayyan, Ryan J. Carlson, (unknown), Ming K. Lee, Süleyman Gülsüner, Tom Walsh, Karen B. Avraham, Moien Kanaan, Mary‐Claire King	0
3	Association of Genetic Diagnoses for Childhood-Onset Hearing Loss With Cochlear Implant Outcomes 2023 ·JAMA Otolaryngology–Head & Neck Surgery ·Ryan J. Carlson, Tom Walsh, Jessica B. Mandell, Amal Abu Rayyan, Ming K. Lee, Süleyman Gülsüner, David L. Horn, Henry C. Ou, Kathleen C.Y. Sie, Lisa R. Mancl, Jay T. Rubinstein, Mary‐Claire King	20
4	Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy, and enteropathy, and implications for clinical management 2021 ·Journal of Allergy and Clinical Immunology ·Sarah K. Baxter, Tom Walsh, Silvia Casadei, (unknown), Eric J. Allenspach, David Hagin, Gesmar Rodrigues Silva Segundo, Ming K. Lee, Süleyman Gülsüner, Brian H. Shirts, Kathleen E. Sullivan, Michael D. Keller, Troy R. Torgerson, Mary‐Claire King	21
5	Genomic analysis of inherited hearing loss in the Palestinian population 2020 ·Proceedings of the National Academy of Sciences ·Amal Abu Rayyan, (unknown), Silvia Casadei, Zippora Brownstein, (unknown), Hashem Shahin, Christina Canavati, (unknown), (unknown), (unknown), Ryan J. Carlson, Süleyman Gülsüner, Ming K. Lee, Karen B. Avraham, Tom Walsh, Mary‐Claire King, Moien Kanaan	38
6	Identifying Inherited and Acquired Genetic Factors Involved in Poor Stem Cell Mobilization and Donor-Derived Malignancy 2016 ·Biology of Blood and Marrow Transplantation ·(unknown), (unknown), Barbara Neistadt, Rafael Márquez, Amittha Wickrema, Andrew Artz, Koen van Besien, Richard A. Larson, Ming K. Lee, Jeremy Segal, Mary‐Claire King, Tom Walsh, Akiko Shimamura, Sioḃán Keel, Jane E. Churpek, Lucy A. Godley	32
7	FAM111B Mutation Is Associated With Inherited Exocrine Pancreatic Dysfunction 2015 ·Pancreas ·(unknown), Tom Walsh, Ming K. Lee, Phoenix A. Ho, Evelyn Hsu, Robert Sidbury, Mary‐Claire King, Akiko Shimamura	27
8	Genetic characterization of early onset ovarian carcinoma 2015 ·Gynecologic Oncology ·Sarah S. Bernards, Barbara M. Norquist, Maria I. Harrell, Kathy Agnew, Ming K. Lee, Tom Walsh, Elizabeth M. Swisher	15
9	Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas breakdown → 2013 ·Clinical Cancer Research ·Kathryn P. Pennington, Tom Walsh, Maria I. Harrell, Ming K. Lee, Christopher C. Pennil, Mara H. Rendi, Anne Thornton, Barbara M. Norquist, Silvia Casadei, Alex S. Nord, Kathy Agnew, Colin C. Pritchard, Sheena Scroggins, Rochelle L. Garcia, Mary‐Claire King, Elizabeth M. Swisher	712
10	Formation of Chimeric Genes by Copy-Number Variation as a Mutational Mechanism in Schizophrenia 2013 ·The American Journal of Human Genetics ·(unknown), Tom Walsh, Süleyman Gülsüner, (unknown), Alex S. Nord, Molly Gasperini, Sarah B. Pierce, Cailyn H. Spurrell, Bradley P. Coe, Niklas Krumm, Ming K. Lee, Jonathan Sebat, Jon McClellan, Mary‐Claire King	28
11	Mutations in LARS2, Encoding Mitochondrial Leucyl-tRNA Synthetase, Lead to Premature Ovarian Failure and Hearing Loss in Perrault Syndrome 2013 ·The American Journal of Human Genetics ·Sarah B. Pierce, Ksenija Geršak, Rachel Michaelson‐Cohen, Tom Walsh, Ming K. Lee, (unknown), Rachel E. Klevit, Mary‐Claire King, Ephrat Levy‐Lahad	152
12	Characteristics of women with ovarian carcinoma who have BRCA1 and BRCA2 mutations not identified by clinical testing 2012 ·Gynecologic Oncology ·Barbara M. Norquist, Kathryn P. Pennington, Kathy Agnew, Maria I. Harrell, Christopher C. Pennil, Ming K. Lee, Silvia Casadei, Anne Thornton, Rochelle L. Garcia, Tom Walsh, Elizabeth M. Swisher	21
13	Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria 2011 ·Proceedings of the National Academy of Sciences ·Sarah B. Pierce, Cailyn H. Spurrell, Jessica B. Mandell, Ming K. Lee, Sharon Zeligson, Michael S. Bereman, Sunday M. Stray, Siv Fokstuen, Michael J. MacCoss, Ephrat Levy‐Lahad, Mary‐Claire King, Arno G. Motulsky	11
14	Contribution of Inherited Mutations in the BRCA2-Interacting Protein PALB2 to Familial Breast Cancer 2011 ·Cancer Research ·Silvia Casadei, Barbara M. Norquist, Tom Walsh, Sunday M. Stray, Jessica B. Mandell, Ming K. Lee, J Stamatoyannopoulos, Mary‐Claire King	182
15	Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing breakdown → 2011 ·Proceedings of the National Academy of Sciences ·Tom Walsh, Silvia Casadei, Ming K. Lee, Christopher C. Pennil, Alex S. Nord, Anne Thornton, Wendy Roeb, Kathy Agnew, Sunday M. Stray, Anneka Wickramanayake, Barbara M. Norquist, Kathryn P. Pennington, Rochelle L. Garcia, Mary‐Claire King, Elizabeth M. Swisher	662
16	Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82 2010 ·The American Journal of Human Genetics ·Tom Walsh, Hashem Shahin, T. Elkan Miller, Ming K. Lee, Anne Thornton, Wendy Roeb, Amal Abu Rayyan, (unknown), Karen B. Avraham, Mary‐Claire King, Moien Kanaan	198
17	Genomic Duplication and Overexpression of TJP2/ZO-2 Leads to Altered Expression of Apoptosis Genes in Progressive Nonsyndromic Hearing Loss DFNA51 2010 ·The American Journal of Human Genetics ·Tom Walsh, Sarah B. Pierce, Danielle R. Lenz, Zippora Brownstein, Orit Dagan‐Rosenfeld, Hashem Shahin, Wendy Roeb, Shane McCarthy, Alex S. Nord, Carlos R. Gordon, Ziva Ben‐Neriah, Jonathan Sebat, Moien Kanaan, Ming K. Lee, Moshe Frydman, Mary‐Claire King, Karen B. Avraham	74
18	Mutations in a Novel Isoform of TRIOBP That Encodes a Filamentous-Actin Binding Protein Are Responsible for DFNB28 Recessive Nonsyndromic Hearing Loss 2005 ·The American Journal of Human Genetics ·Hashem Shahin, Tom Walsh, Tama Sobe, (unknown), Amal Rayan, Eric D. Lynch, Ming K. Lee, Karen B. Avraham, Mary‐Claire King, Moien Kanaan	85
19	From flies' eyes to our ears: Mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30 2002 ·Proceedings of the National Academy of Sciences ·Tom Walsh, (unknown), Sarah Vreugde, Ronna Hertzano, Hashem Shahin, (unknown), Ming K. Lee, Moien Kanaan, Mary‐Claire King, Karen B. Avraham	170
20	SeqHelp: A Program to Analyze Molecular Sequences Utilizing Common Computational Resources 1998 ·Genome Research ·Ming K. Lee, Eric D. Lynch, Mary‐Claire King	26

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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