Lynn R. Goldin mainly investigates Genetics, Internal medicine, Immunology, Genetic linkage and Oncology. His Genetics study frequently draws connections between adjacent fields such as Bipolar disorder. His work on Case-control study, Risk factor, Odds ratio and Family aggregation as part of his general Internal medicine study is frequently connected to Monoclonal gammopathy of undetermined significance, thereby bridging the divide between different branches of science.
His studies examine the connections between Immunology and genetics, as well as such issues in Relative risk, with regards to Age of onset. His Genetic linkage research incorporates themes from Genome, Genome Scan, Schizoaffective disorder and Chromosome, Gene mapping. His work carried out in the field of Locus brings together such families of science as Psychosis and Genome-wide association study.
His primary areas of investigation include Genetics, Internal medicine, Immunology, Chronic lymphocytic leukemia and Genetic linkage. His work is connected to Locus, Pedigree chart, Linkage, Genetic marker and Genotype, as a part of Genetics. Many of his research projects under Internal medicine are closely connected to Monoclonal gammopathy of undetermined significance with Monoclonal gammopathy of undetermined significance, tying the diverse disciplines of science together.
His Immunology research is multidisciplinary, incorporating perspectives in Family aggregation and Family history. Lynn R. Goldin focuses mostly in the field of Chronic lymphocytic leukemia, narrowing it down to topics relating to Genome-wide association study and, in certain cases, Genetic association. Lynn R. Goldin works mostly in the field of Genetic linkage, limiting it down to topics relating to Genetic heterogeneity and, in certain cases, Psychiatry, as a part of the same area of interest.
Lynn R. Goldin mostly deals with Internal medicine, Genetics, Immunology, Chronic lymphocytic leukemia and Waldenstrom macroglobulinemia. His work on Internal medicine is being expanded to include thematically relevant topics such as Oncology. His Oncology research is multidisciplinary, incorporating elements of Family aggregation, Single-nucleotide polymorphism and Myeloid leukemia.
His Immunology study incorporates themes from Survival analysis, Malignancy and Case-control study. His study looks at the relationship between Chronic lymphocytic leukemia and fields such as Cancer, as well as how they intersect with chemical problems. The concepts of his Waldenstrom macroglobulinemia study are interwoven with issues in Gastroenterology, Disease and Meningitis.
Lynn R. Goldin mainly focuses on Genetics, Genetic association, Genome-wide association study, Internal medicine and Leukemia. His research brings together the fields of Physiology and Genetics. His work in Genetic association covers topics such as SNP array which are related to areas like Karyotype, Confidence interval and Uniparental disomy.
In his study, which falls under the umbrella issue of Genome-wide association study, Single-nucleotide polymorphism, B-cell lymphoma and Linkage disequilibrium is strongly linked to Locus. Lynn R. Goldin combines subjects such as Immunology and Oncology with his study of Internal medicine. His study in the field of Hematology and Multiple myeloma also crosses realms of Monoclonal gammopathy of undetermined significance.
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A Family Study of Schizoaffective, Bipolar I, Bipolar II, Unipolar, and Normal Control Probands
Elliot S. Gershon;Joel Hamovit;Juliet J. Guroff;Eleanor Dibble.
Archives of General Psychiatry (1982)
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.
Ricardo Segurado;Sevilla D. Detera-Wadleigh;Douglas F. Levinson;Cathryn M. Lewis.
American Journal of Human Genetics (2003)
A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma.
Maria Teresa Landi;Nilanjan Chatterjee;Kai Yu;Lynn R. Goldin.
American Journal of Human Genetics (2009)
Detectable clonal mosaicism and its relationship to aging and cancer
Kevin B. Jacobs;Kevin B. Jacobs;Meredith Yeager;Meredith Yeager;Weiyin Zhou;Weiyin Zhou;Sholom Wacholder.
Nature Genetics (2012)
A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2
Sevilla D. Detera-Wadleigh;Judith A. Badner;Judith A. Badner;Wade H. Berrettini;Takeo Yoshikawa.
Proceedings of the National Academy of Sciences of the United States of America (1999)
Chromosome 18 DNA markers and manic-depressive illness: evidence for a susceptibility gene
Wade H. Berrettini;Thomas N. Ferraro;Lynn R. Goldin;Daniel E. Weeks.
Proceedings of the National Academy of Sciences of the United States of America (1994)
Detectable clonal mosaicism from birth to old age and its relationship to cancer
Cathy C. Laurie;Cecelia A Laurie;Kenneth Rice;Kimberly F. Doheny.
Nature Genetics (2012)
Risk of monoclonal gammopathy of undetermined significance (MGUS) and subsequent multiple myeloma among African American and white veterans in the United States
Ola Landgren;Gloria Gridley;Ingemar Turesson;Neil E. Caporaso.
Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 1, 6, 8, 10, and 12.
John P. Rice;Alison Goate;Jeff T. Williams;Laura Bierut.
American Journal of Medical Genetics (1997)
Variant Genotypes of the Low-Affinity Fcγ Receptors in Two Control Populations and a Review of Low-Affinity Fcγ Receptor Polymorphisms in Control and Disease Populations
Thomas Lehrnbecher;Charles B. Foster;Shaoxian Zhu;Susan F. Leitman.
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