D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics and Molecular Biology D-index 43 Citations 18,919 60 World Ranking 4662 National Ranking 2172

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Mutation
  • Genetics

Ming K. Lee mostly deals with Genetics, Gene, Cancer research, Mutation and Breast cancer. His works in Genetic testing, Nonsense mutation, Frameshift mutation, Mammary gland and Genetic analysis are all subjects of inquiry into Genetics. His work on Transcriptional regulation, Transcriptome and Gene regulatory network as part of his general Gene study is frequently connected to Human brain and Ventrolateral prefrontal cortex, thereby bridging the divide between different branches of science.

His study explores the link between Cancer research and topics such as Point mutation that cross with problems in Ovarian carcinoma and Fallopian tube carcinoma. His Mutation research is multidisciplinary, incorporating elements of Gene duplication, Human genome, Bioinformatics and Neurodevelopmental disorder. The concepts of his Breast cancer study are interwoven with issues in Chromosome, Gene mapping and Disease.

His most cited work include:

  • Linkage of early-onset familial breast cancer to chromosome 17q21 (2040 citations)
  • Initial sequence of the chimpanzee genome and comparison with the human genome (1915 citations)
  • Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia (1517 citations)

What are the main themes of his work throughout his whole career to date?

Ming K. Lee spends much of his time researching Genetics, Internal medicine, Mutation, Breast cancer and Gene. Borrowing concepts from Hearing loss, Ming K. Lee weaves in ideas under Genetics. His study in Internal medicine is interdisciplinary in nature, drawing from both Immunology, Endocrinology and Oncology.

The Breast cancer study combines topics in areas such as CHEK2, Ovarian cancer, Disease and PALB2. He has researched Disease in several fields, including Chromosome and Gene mapping. His Cancer study combines topics in areas such as Germline mutation and Cancer research.

He most often published in these fields:

  • Genetics (54.90%)
  • Internal medicine (25.49%)
  • Mutation (25.49%)

What were the highlights of his more recent work (between 2017-2021)?

  • Mutation (25.49%)
  • Internal medicine (25.49%)
  • Genetics (54.90%)

In recent papers he was focusing on the following fields of study:

His main research concerns Mutation, Internal medicine, Genetics, Gene and Germline mutation. His Mutation research incorporates themes from Transplantation and Bioinformatics. His Internal medicine research incorporates elements of Gastroenterology and Oncology.

His Oncology research is multidisciplinary, relying on both Breast cancer and Inherited Predisposition. Ming K. Lee undertakes multidisciplinary investigations into Genetics and Hearing loss in his work. His work in Germline mutation addresses issues such as Germline, which are connected to fields such as Exome sequencing, CHEK2, Carcinoma and Fallopian tube.

Between 2017 and 2021, his most popular works were:

  • Inherited predisposition to malignant mesothelioma and overall survival following platinum chemotherapy (44 citations)
  • Inherited Breast Cancer in Nigerian Women (32 citations)
  • Characterization of splice-altering mutations in inherited predisposition to cancer. (8 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Mutation
  • DNA

His primary areas of study are Gene, Mutation, Internal medicine, Oncology and Intron. His Gene study incorporates themes from Prostate and Peritoneal mesothelioma. Many of his studies involve connections with topics such as Mesothelioma and Mutation.

His study in Genetic testing, Family history, Breast cancer, Stage and Disease is carried out as part of his Internal medicine studies. His research integrates issues of Cancer, Inherited Predisposition and Hormone receptor in his study of Oncology. His Intron research is classified as research in Genetics.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Linkage of early-onset familial breast cancer to chromosome 17q21

Jeff M. Hall;Ming K. Lee;Beth Newman;Jan E. Morrow.
Science (1990)

3198 Citations

Initial sequence of the chimpanzee genome and comparison with the human genome

Tarjei S. Mikkelsen;LaDeana W. Hillier.
Nature (2005)

1945 Citations

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

Tom Walsh;Jon M. McClellan;Shane E. McCarthy;Anjené M. Addington.
Science (2008)

1938 Citations

Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

Tom Walsh;Silvia Casadei;Ming K. Lee;Christopher C. Pennil.
Proceedings of the National Academy of Sciences of the United States of America (2011)

828 Citations

Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer.

Tom Walsh;Silvia Casadei;Kathryn Hale Coats;Elizabeth Swisher.
JAMA (2006)

802 Citations

Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas

Kathryn P. Pennington;Tom Walsh;Maria I. Harrell;Ming K. Lee.
Clinical Cancer Research (2014)

645 Citations

Nonsyndromic Deafness DFNA1 Associated with Mutation of a Human Homolog of the Drosophila Gene diaphanous

Eric D. Lynch;Ming K. Lee;Jan E. Morrow;Piri L. Welcsh.
Science (1997)

537 Citations

Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

Tom Walsh;Ming K. Lee;Silvia Casadei;Anne M. Thornton.
Proceedings of the National Academy of Sciences of the United States of America (2010)

484 Citations

Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network

Suleyman Gulsuner;Tom Walsh;Amanda C. Watts;Ming K. Lee.
Cell (2013)

475 Citations

Inherited Mutations in Women With Ovarian Carcinoma

Barbara M. Norquist;Maria I. Harrell;Mark F. Brady;Tom Walsh.
JAMA Oncology (2016)

446 Citations

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