Biography:Mark Lathrop
From HandWiki
Short description: Canadian Biostatistician (born 1950)
Mark Lathrop | |
|---|---|
| Born | 1950 |
| Citizenship | Canada |
| Scientific career | |
| Fields | Biostatistics |
| Institutions | Center for the Study of Human Polymorphisms |
Mark Lathrop (born 1950) is a Canadian Biostatistician. He headed the Center for the Study of Human Polymorphisms, but returned to Canada as Scientific Director at McGill University and Genome Quebec's Innovation Centre in 2011.[1]
Bibliography
- Hung, Rayjean J et al. (April 2008). "A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25". Nature 452 (7187): 633–7. doi:10.1038/nature06885. PMID 18385738. Bibcode: 2008Natur.452..633H. https://hal-cea.archives-ouvertes.fr/cea-00944415/file/Hung1.pdf.
- Moffatt, Miriam F et al. (July 2007). "Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma". Nature 448 (7152): 470–3. doi:10.1038/nature06014. PMID 17611496. Bibcode: 2007Natur.448..470M. https://deepblue.lib.umich.edu/bitstream/2027.42/62682/1/nature06014.pdf.
- Bouzigon, Emmanuelle; Corda Eve; Aschard Hugues; Dizier Marie-Hélène; Boland Anne; Bousquet Jean; Chateigner Nicolas; Gormand Frédéric et al. (November 2008). "Effect of 17q21 variants and smoking exposure in early-onset asthma". N. Engl. J. Med. 359 (19): 1985–94. doi:10.1056/NEJMoa0806604. PMID 18923164.
- Spanagel, Rainer; Pendyala Gurudutt; Abarca Carolina; Zghoul Tarek; Sanchis-Segura Carles; Magnone Maria Chiara; Lascorz Jesús; Depner Martin et al. (January 2005). "The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption". Nat. Med. 11 (1): 35–42. doi:10.1038/nm1163. ISSN 1078-8956. PMID 15608650. http://doc.rero.ch/record/4324/files/1_albrecht_cgp.pdf.
- Kathiresan, S et al. (December 2008). "Common variants at 30 loci contribute to polygenic dyslipidemia". Nat. Genet. 41 (1): 56–65. doi:10.1038/ng.291. PMID 19060906.
- McKay, James D et al. (December 2008). "Lung cancer susceptibility locus at 5p15.33". Nat. Genet. 40 (12): 1404–6. doi:10.1038/ng.254. PMID 18978790.
- Barrett, Jeffrey C et al. (August 2008). "Genome-wide association defines more than thirty distinct susceptibility loci for Crohn's disease". Nat. Genet. 40 (8): 955–62. doi:10.1038/ng.175. PMID 18587394.
- Saar Kathrin (May 2008). "SNP and haplotype mapping for genetic analysis in the rat". Nat. Genet. 40 (5): 560–6. doi:10.1038/ng.124. PMID 18443594.
- Willer, Cristen J; Sanna, S; Jackson, AU; Scuteri, A; Bonnycastle, LL; Clarke, R; Heath, SC; Timpson, NJ et al. (February 2008). "Newly identified loci that influence lipid concentrations and risk of coronary artery disease". Nat. Genet. 40 (2): 161–9. doi:10.1038/ng.76. PMID 18193043.
- Wellcome Trust Case Control Consortium; Australo-Anglo-American Spondylitis Consortium (TASC); Burton, PR; Clayton, DG; Cardon, LR; Craddock, N; Deloukas, P; Duncanson, A et al. (November 2007). "Association scan of 14,500 nsSNPs in four common diseases identifies variants involved in autoimmunity". Nat. Genet. 39 (11): 1329–37. doi:10.1038/ng.2007.17. PMID 17952073.
- Dixon, Anna L; Liang Liming; Moffatt Miriam F; Chen Wei; Heath Simon; Wong Kenny C C; Taylor Jenny; Burnett Edward et al. (October 2007). "A genome-wide association study of global gene expression". Nat. Genet. 39 (10): 1202–7. doi:10.1038/ng2109. PMID 17873877.
- Menzel, Stephan; Garner Chad; Gut Ivo; Matsuda Fumihiko; Yamaguchi Masao; Heath Simon; Foglio Mario; Zelenika Diana et al. (October 2007). "A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15". Nat. Genet. 39 (10): 1197–9. doi:10.1038/ng2108. PMID 17767159.
- Fischer, Judith; Lefèvre Caroline; Morava Eva; Mussini Jean-Marie; Laforêt Pascal; Negre-Salvayre Anne; Lathrop Mark; Salvayre Robert (January 2007). "The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy". Nat. Genet. 39 (1): 28–30. doi:10.1038/ng1951. ISSN 1061-4036. PMID 17187067.
- Delmaghani, Sedigheh; del Castillo Francisco J; Michel Vincent; Leibovici Michel; Aghaie Asadollah; Ron Uri; Van Laer Lut; Ben-Tal Nir et al. (July 2006). "Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy". Nat. Genet. 38 (7): 770–8. doi:10.1038/ng1829. ISSN 1061-4036. PMID 16804542.
- Sakuntabhai, Anavaj; Turbpaiboon, C; Casadémont, I; Chuansumrit, A; Lowhnoo, T; Kajaste-Rudnitski, A; Kalayanarooj, SM; Tangnararatchakit, K et al. (May 2005). "A variant in the CD209 promoter is associated with severity of dengue disease". Nat. Genet. 37 (5): 507–13. doi:10.1038/ng1550. ISSN 1061-4036. PMID 15838506.
- Auwerx, Johan; Avner, P; Baldock, R; Ballabio, A; Balling, R; Barbacid, M; Berns, A; Bradley, A et al. (September 2004). "The European dimension for the mouse genome mutagenesis program". Nat. Genet. 36 (9): 925–7. doi:10.1038/ng0904-925. ISSN 1061-4036. PMID 15340424.
- Gut, Ivo G; Lathrop G Mark (August 2004). "Duplicating SNPs". Nat. Genet. 36 (8): 789–90. doi:10.1038/ng0804-789. ISSN 1061-4036. PMID 15284844.
- Allen, Maxine; Heinzmann Andrea; Noguchi Emiko; Abecasis Gonçalo; Broxholme John; Ponting Chris P; Bhattacharyya Sumit; Tinsley Jon et al. (November 2003). "Positional cloning of a novel gene influencing asthma from chromosome 2q14". Nat. Genet. 35 (3): 258–63. doi:10.1038/ng1256. ISSN 1061-4036. PMID 14566338.
- Caulfield, Mark; Munroe Patricia; Pembroke Janine; Samani Nilesh; Dominiczak Anna; Brown Morris; Benjamin Nigel; Webster John et al. (June 2003). "Genome-wide mapping of human loci for essential hypertension". Lancet 361 (9375): 2118–23. doi:10.1016/S0140-6736(03)13722-1. PMID 12826435.
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