Richard A. Gibbs, Ph.D
Affiliations: | 1991-2001 | Pharmacy | Wayne State University, Detroit, MI, United States |
2001-2014 | Pharmacy | Purdue University, West Lafayette, IN, United States |
Website:
http://www.legacy.com/obituaries/jconline/obituary.aspx?n=richard-a-gibbs&pid=169689198&fhid=17363Google:
"Richard Anthony Gibbs"Bio:
(1961 - 2014)
http://cnas.ucr.edu/chem50th/speakers.html
Mean distance: 8.1 | S | N | B | C | P |
Parents
Sign in to add mentorWilliam H. Okamura | grad student | 1988 | UC Riverside | |
(An enantioselective central-axial-central chiral element transfer process leading to a concise synthesis of (+)-sterpurene : intramolecular Diels-Alder reactions of vinylallene sulfoxides ; and, Synthesis of 9 (11)-dehydrovitamin D₃ analogues) | ||||
Stephen J. Benkovic | post-doc | 1988-1991 | Penn State |
Children
Sign in to add traineeBrian S. Henriksen | grad student | 2005 | Purdue |
Sarah A. Reigard | grad student | 2006 | Purdue |
Animesh V. Aditya | grad student | 2010 | Purdue |
Jiao Song | grad student | 2010 | Purdue |
Kayla J. Temple | grad student | 2007-2013 | Purdue |
Diwan S Rawat | post-doc | 2001-2002 | Purdue |
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Publications
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Gibbs RA. (2020) The Human Genome Project changed everything. Nature Reviews. Genetics |
Sabo A, Murdock D, Dugan S, et al. (2020) Community-based recruitment and exome sequencing indicates high diagnostic yield in adults with intellectual disability. Molecular Genetics & Genomic Medicine. e1439 |
Yuan B, Wang L, Liu P, et al. (2020) CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indels. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
Oeyen JP, Baa-Puyoulet P, Benoit JB, et al. (2020) Sawfly genomes reveal evolutionary acquisitions that fostered the mega-radiation of parasitoid and eusocial Hymenoptera. Genome Biology and Evolution |
Narita TB, Kawabe Y, Kin K, et al. (2020) Loss of the polyketide synthase StlB results in stalk cell overproduction in Polysphondylium violaceum. Genome Biology and Evolution |
Gonzaga-Jauregui C, Yesil G, Nistala H, et al. (2020) Functional biology of the Steel syndrome founder allele and evidence for clan genomics derivation of COL27A1 pathogenic alleles worldwide. European Journal of Human Genetics : Ejhg |
Schloss JA, Gibbs RA, Makhijani VB, et al. (2020) Cultivating DNA Sequencing Technology After the Human Genome Project. Annual Review of Genomics and Human Genetics |
Thomas GWC, Dohmen E, Hughes DST, et al. (2020) Gene content evolution in the arthropods. Genome Biology. 21: 15 |
Chen CA, Pal R, Yin J, et al. (2020) Combination of whole exome sequencing and animal modeling identifies TMPRSS9 as a candidate gene for autism spectrum disorder. Human Molecular Genetics |
Tosur M, Sabo A, Khayat MM, et al. (2020) 1550-P: Whole-Exome Sequencing in Children with Suspected Maturity-Onset Diabetes of the Young (MODY) Diabetes. 69 |