2023 - Research.com Genetics in United States Leader Award
2012 - Fellow of the American Academy of Arts and Sciences
2001 - Member of the National Academy of Sciences
Richard P. Lifton focuses on Genetics, Internal medicine, Endocrinology, Mutation and Gene. His Genetics study frequently links to related topics such as Disease. His work on Bartter's syndrome, Bartter syndrome and Hyperaldosteronism as part of general Internal medicine research is frequently linked to CLCNKB and Gitelman syndrome, bridging the gap between disciplines.
Richard P. Lifton works mostly in the field of Endocrinology, limiting it down to topics relating to Missense mutation and, in certain cases, Wnt signaling pathway. His Mutation study combines topics in areas such as Mutant and Epithelial sodium channel. His research investigates the connection between Gene and topics such as Molecular biology that intersect with issues in T cell, Protein subunit, Glucocorticoid remediable aldosteronism, Aldosterone synthase and Ectopic expression.
His primary scientific interests are in Genetics, Internal medicine, Exome sequencing, Mutation and Endocrinology. His Genetics study is mostly concerned with Gene, Allele, Locus, Genetic linkage and Genome-wide association study. His work deals with themes such as Disease and Bioinformatics, which intersect with Gene.
His study ties his expertise on Oncology together with the subject of Internal medicine. His Exome sequencing research includes themes of Cancer research, Proband and Germline mutation. The various areas that Richard P. Lifton examines in his Mutation study include Phenotype and Molecular biology.
His primary areas of investigation include Exome sequencing, Genetics, Mutation, Gene and Internal medicine. His Exome sequencing research is multidisciplinary, relying on both Cancer research, Germline mutation and Kidney disease. As a part of the same scientific study, Richard P. Lifton usually deals with the Genetics, concentrating on Disease and frequently concerns with Phenocopy.
He interconnects Phenotype, Nephrotic syndrome, Gene knockdown and Genotype in the investigation of issues within Mutation. His Gene study deals with Bioinformatics intersecting with Genetic heterogeneity. His studies in Internal medicine integrate themes in fields like Endocrinology and Oncology.
His scientific interests lie mostly in Exome sequencing, Genetics, Mutation, Cancer research and Gene. He combines subjects such as Germline mutation, Internal medicine, Kidney disease and Phenocopy with his study of Exome sequencing. In his research, Candidate gene is intimately related to Pediatrics, which falls under the overarching field of Internal medicine.
His studies deal with areas such as Endocrinology, Gene knockdown, Phenotype, Nuclear pore and Zebrafish as well as Mutation. His work deals with themes such as PTEN, Pathogenesis, Nephrotic syndrome, Carcinoma and Adjuvant therapy, which intersect with Cancer research. The concepts of his Gene study are interwoven with issues in Computational biology, Bioinformatics and Macaque.
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Molecular basis of human hypertension: Role of angiotensinogen
Xavier Jeunemaitre;Florent Soubrier;Yuri V. Kotelevtsev;Richard P. Lifton;Richard P. Lifton.
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
Stephan J. Sanders;Michael T. Murtha;Abha R. Gupta;John D. Murdoch.
Molecular Mechanisms of Human Hypertension
Richard P. Lifton;Ali G. Gharavi;Ali G. Gharavi;David S. Geller.
High Bone Density Due to a Mutation in LDL-Receptor–Related Protein 5
Lynn M. Boyden;Junhao Mao;Joseph Belsky;Lyle Mitzner.
The New England Journal of Medicine (2002)
Genetic studies of body mass index yield new insights for obesity biology
Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice.
Faculty of Health; Institute of Health and Biomedical Innovation (2015)
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
Murim Choi;Ute I. Scholl;Weizhen Ji;Tiewen Liu.
Proceedings of the National Academy of Sciences of the United States of America (2009)
Autoantibodies against type I IFNs in patients with life-threatening COVID-19.
Paul Bastard;Paul Bastard;Paul Bastard;Lindsey B. Rosen;Qian Zhang;Eleftherios Michailidis.
Human hypertension caused by mutations in WNK kinases
Frederick H. Wilson;Sandra Disse-Nicodème;Keith A. Choate;Kazuhiko Ishikawa.
Liddle's syndrome: Heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channel
Richard A. Shimkets;David G. Warnock;Christopher M. Bositis;Carol Nelson-Williams.
A chimaeric 11 beta-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension.
Richard P. Lifton;Robert G. Dluhy;Michael Powers;Glenn M. Rich.
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