2005 - Member of the National Academy of Sciences
1986 - Fellow of the MacArthur Foundation
Genetics, Y chromosome, Gene, X chromosome and Azoospermia factor are his primary areas of study. His work on Genetics deals in particular with Gene mapping, Genome, Homologous chromosome, X-inactivation and Chromosome 21. His Y chromosome study combines topics in areas such as Y chromosome microdeletion, Azoospermia, Gene family, Molecular biology and Homology.
His X chromosome study integrates concerns from other disciplines, such as Chromosome, Sex linkage and Karyotype. His research investigates the connection between Azoospermia factor and topics such as Homologous recombination that intersect with issues in Breakpoint. His Somatic cell study also includes
David C. Page mostly deals with Genetics, Y chromosome, Gene, Artificial intelligence and X chromosome. His Genetics study often links to related topics such as Molecular biology. While the research belongs to areas of Y chromosome, he spends his time largely on the problem of Chromosome 21, intersecting his research to questions surrounding Chromosome 16 and Chromosome 4.
His research on Gene often connects related areas such as Evolutionary biology. His Artificial intelligence study combines topics in areas such as Machine learning and Statistical relational learning. His X chromosome research is multidisciplinary, incorporating perspectives in Karyotype, Locus and Homology.
David C. Page mainly investigates Cell biology, Gene, Artificial intelligence, Machine learning and Germ cell. David C. Page has included themes like DAZL, Meiosis, Prophase and Germline in his Cell biology study. His study on Gene is covered under Genetics.
He studies Chromosome which is a part of Genetics. His Germ cell study which covers Gonad that intersects with Ovary, Sexual differentiation, Sperm and Retinoic acid. His Y chromosome research is multidisciplinary, relying on both Initiation factor and Copy-number variation.
His primary areas of investigation include Gene, Cell biology, Germline, Gene expression and Genetics. The concepts of his Gene study are interwoven with issues in Sex characteristics and DNA. The Cell biology study combines topics in areas such as DAZL, Meiosis, Germ cell and Transcription.
In his research on the topic of Germline, Homologous chromosome, DNA damage, Mutant, Embryo and Topoisomerase is strongly related with DNA replication. David C. Page integrates Genetics and EIF1AX in his research. His study in Y chromosome is interdisciplinary in nature, drawing from both Autosome, Amplicon, Dosage compensation, Phylogenetics and 1000 Genomes Project.
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The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes.
Helen Skaletsky;Tomoko Kuroda-Kawaguchi;Patrick J. Minx;Holland S. Cordum.
Estimation of the warfarin dose with clinical and pharmacogenetic data
Klein Te;Altman Rb;Eriksson N.
The New England Journal of Medicine (2009)
Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein gene
Renee Reijo;Tien-Yi Lee;Pia Salo;Raaji Alagappan.
Nature Genetics (1995)
A gene map of the human genome
G. D. Schuler;M. S. Boguski;E. A. Stewart;L. D. Stein.
Genome maps 7. The human transcript map. Wall chart.
G. D. Schuler;M. S. Boguski;T. J. Hudson;L. Hui.
A comprehensive genetic map of the mouse genome
William F. Dietrich;Joyce Miller;Robert Steen;Mark A. Merchant.
The sex-determining region of the human Y chromosome encodes a finger protein
David C. Page;Rebecca Mosher;Elizabeth M. Simpson;Elizabeth M.C. Fisher.
Four Evolutionary Strata on the Human X Chromosome
Bruce T. Lahn;David C. Page.
Functional coherence of the human Y chromosome.
Bruce T. Lahn;David C. Page.
An STS-Based Map of the Human Genome
Thomas J. Hudson;Lincoln D. Stein;Sebastian S. Gerety;Junli Ma.
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