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.
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.
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.
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.
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Linkage of early-onset familial breast cancer to chromosome 17q21
Jeff M. Hall;Ming K. Lee;Beth Newman;Jan E. Morrow.
Initial sequence of the chimpanzee genome and comparison with the human genome
Tarjei S. Mikkelsen;LaDeana W. Hillier.
Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
Tom Walsh;Jon M. McClellan;Shane E. McCarthy;Anjené M. Addington.
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)
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.
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)
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.
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)
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.
Inherited Mutations in Women With Ovarian Carcinoma
Barbara M. Norquist;Maria I. Harrell;Mark F. Brady;Tom Walsh.
JAMA Oncology (2016)
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