Mark Lathrop

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; McKay James D, Gaborieau Valerie, .... Lathrop Mark, Brennan Paul (April 2008). "A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25". Nature. England. 452 (7187): 633–7. Bibcode:2008Natur.452..633H. doi:10.1038/nature06885. PMID 18385738.  Cite uses deprecated parameter |coauthors= (help)
• Moffatt, Miriam F; Kabesch Michael, .... Lathrop G Mark, Cookson William O C (July 2007). "Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma". Nature. England. 448 (7152): 470–3. Bibcode:2007Natur.448..470M. doi:10.1038/nature06014. PMID 17611496.  Cite uses deprecated parameter |coauthors= (help)
• Bouzigon, Emmanuelle; Corda Eve, Aschard Hugues, Dizier Marie-Hélène, Boland Anne, Bousquet Jean, Chateigner Nicolas, Gormand Frédéric, Just Jocelyne, Le Moual Nicole, Scheinmann Pierre, Siroux Valérie, Vervloet Daniel, Zelenika Diana, Pin Isabelle, Kauffmann Francine, Lathrop Mark, Demenais Florence (November 2008). "Effect of 17q21 variants and smoking exposure in early-onset asthma". N. Engl. J. Med. United States. 359 (19): 1985–94. doi:10.1056/NEJMoa0806604. PMID 18923164.  Cite uses deprecated parameter |coauthors= (help)
• Spanagel, Rainer; Pendyala Gurudutt, Abarca Carolina, Zghoul Tarek, Sanchis-Segura Carles, Magnone Maria Chiara, Lascorz Jesús, Depner Martin, Holzberg David, Soyka Michael, Schreiber Stefan, Matsuda Fumihiko, Lathrop Mark, Schumann Gunter, Albrecht Urs (January 2005). "The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption". Nat. Med. United States. 11 (1): 35–42. doi:10.1038/nm1163. ISSN 1078-8956. PMID 15608650.  Cite uses deprecated parameter |coauthors= (help)
• Kathiresan, S; Willer, Peloso, Demissie, ... Lathrop, Melander, Salomaa, Peltonen, Orho-Melander, Ordovas, Boehnke, Abecasis, Mohlke, Cupples (December 2008). "Common variants at 30 loci contribute to polygenic dyslipidemia". Nat. Genet. 41 (1): 56–65. doi:10.1038/ng.291. PMC 2881676. PMID 19060906.  Cite uses deprecated parameter |coauthors= (help)
• McKay, James D; Hung Rayjean J, ..., Lathrop Mark, Brennan Paul (December 2008). "Lung cancer susceptibility locus at 5p15.33". Nat. Genet. United States. 40 (12): 1404–6. doi:10.1038/ng.254. PMC 2748187. PMID 18978790.  Cite uses deprecated parameter |coauthors= (help)
• Barrett, Jeffrey C; Hansoul Sarah, ... Lathrop Mark..., Daly Mark J (August 2008). "Genome-wide association defines more than thirty distinct susceptibility loci for Crohn's disease". Nat. Genet. United States. 40 (8): 955–62. doi:10.1038/ng.175. PMC 2574810. PMID 18587394.  Cite uses deprecated parameter |coauthors= (help)
• Star, Consortium; Saar Kathrin,...Lathrop G Mark.... Hubner Norbert (May 2008). "SNP and haplotype mapping for genetic analysis in the rat". Nat. Genet. United States. 40 (5): 560–6. doi:10.1038/ng.124. PMID 18443594.  Cite uses deprecated parameter |coauthors= (help)
• 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. United States. 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. United States. 39 (11): 1329–37. doi:10.1038/ng.2007.17. PMC 2680141. PMID 17952073. 
• Dixon, Anna L; Liang Liming, Moffatt Miriam F, Chen Wei, Heath Simon, Wong Kenny C C, Taylor Jenny, Burnett Edward, Gut Ivo, Farrall Martin, Lathrop G Mark, Abecasis Gonçalo R, Cookson William O C (October 2007). "A genome-wide association study of global gene expression". Nat. Genet. United States. 39 (10): 1202–7. doi:10.1038/ng2109. PMID 17873877.  Cite uses deprecated parameter |coauthors= (help)
• Menzel, Stephan; Garner Chad, Gut Ivo, Matsuda Fumihiko, Yamaguchi Masao, Heath Simon, Foglio Mario, Zelenika Diana, Boland Anne, Rooks Helen, Best Steve, Spector Tim D, Farrall Martin, Lathrop Mark, Thein Swee Lay (October 2007). "A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15". Nat. Genet. United States. 39 (10): 1197–9. doi:10.1038/ng2108. PMID 17767159.  Cite uses deprecated parameter |coauthors= (help)
• 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. United States. 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, Van Camp Guy, Weil Dominique, Langa Francina, Lathrop Mark, Avan Paul, Petit Christine (July 2006). "Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy". Nat. Genet. United States. 38 (7): 770–8. doi:10.1038/ng1829. ISSN 1061-4036. PMID 16804542.  Cite uses deprecated parameter |coauthors= (help)
• 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. United States. 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. United States. 36 (9): 925–7. doi:10.1038/ng0904-925. ISSN 1061-4036. PMC 2716028. PMID 15340424. 
• Gut, Ivo G; Lathrop G Mark (August 2004). "Duplicating SNPs". Nat. Genet. United States. 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, Zhang Youming, Holt Richard, Jones E Yvonne, Lench Nick, Carey Alisoun, Jones Helene, Dickens Nicholas J, Dimon Claire, Nicholls Rosie, Baker Crystal, Xue Luzheng, Townsend Elizabeth, Kabesch Michael, Weiland Stephan K, Carr David, von Mutius Erika, Adcock Ian M, Barnes Peter J, Lathrop G Mark, Edwards Mark, Moffatt Miriam F, Cookson William O C M (November 2003). "Positional cloning of a novel gene influencing asthma from chromosome 2q14". Nat. Genet. United States. 35 (3): 258–63. doi:10.1038/ng1256. ISSN 1061-4036. PMID 14566338.  Cite uses deprecated parameter |coauthors= (help)
• Caulfield, Mark; Munroe Patricia, Pembroke Janine, Samani Nilesh, Dominiczak Anna, Brown Morris, Benjamin Nigel, Webster John, Ratcliffe Peter, O'Shea Suzanne, Papp Jeanette, Taylor Elizabeth, Dobson Richard, Knight Joanne, Newhouse Stephen, Hooper Joel, Lee Wai, Brain Nick, Clayton David, Lathrop G Mark, Farrall Martin, Connell John, (June 2003). "Genome-wide mapping of human loci for essential hypertension". Lancet. England. 361 (9375): 2118–23. doi:10.1016/S0140-6736(03)13722-1. PMID 12826435.  Cite uses deprecated parameter |coauthors= (help)

References