词条 | Mark Lathrop |
释义 |
|name = Mark Lathrop |birth_date = 1950 |birth_place = |death_date = |death_place = |residence = |citizenship = Canada |nationality = |ethnicity = |field = Biostatistics |work_institutions = Center for the Study of Human Polymorphisms |alma_mater = |doctoral_advisor = |doctoral_students = |known_for = |author_abbrev_bot =|author_abbrev_zoo = |influences = |influenced = |prizes = |religion = |footnotes = |signature = }}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
|last=Hung |first=Rayjean J |author2=McKay James D |author3=Gaborieau Valerie |display-authors=etal |date=April 2008 |title=A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25 |journal=Nature |volume=452 |issue=7187 |pages=633–7 | pmid = 18385738 |doi = 10.1038/nature06885 | bibcode = 2008Natur.452..633H| oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |hdl=2318/102453
|last=Moffatt |first=Miriam F |author2=Kabesch Michael |display-authors=etal |date=July 2007 |title=Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma |journal=Nature |volume=448 |issue=7152 |pages=470–3 | pmid = 17611496 |doi = 10.1038/nature06014 | bibcode = 2007Natur.448..470M| oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote =
|last=Bouzigon |first=Emmanuelle |author2=Corda Eve |author3=Aschard Hugues |author4=Dizier Marie-Hélène |author5=Boland Anne |author6=Bousquet Jean |author7=Chateigner Nicolas |author8=Gormand Frédéric |author9=Just Jocelyne |author10=Le Moual Nicole |author11=Scheinmann Pierre |author12=Siroux Valérie |author13=Vervloet Daniel |author14=Zelenika Diana |author15=Pin Isabelle |author16=Kauffmann Francine |author17=Lathrop Mark |author18=Demenais Florence |date=November 2008 |title=Effect of 17q21 variants and smoking exposure in early-onset asthma |journal=N. Engl. J. Med. |volume=359 |issue=19 |pages=1985–94 | pmid = 18923164 |doi = 10.1056/NEJMoa0806604 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote =
|last=Spanagel |first=Rainer |author2=Pendyala Gurudutt |author3=Abarca Carolina |author4=Zghoul Tarek |author5=Sanchis-Segura Carles |author6=Magnone Maria Chiara |author7=Lascorz Jesús |author8=Depner Martin |author9=Holzberg David |author10=Soyka Michael |author11=Schreiber Stefan |author12=Matsuda Fumihiko |author13=Lathrop Mark |author14=Schumann Gunter |author15=Albrecht Urs |date=January 2005 |title=The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption |journal=Nat. Med. |volume=11 |issue=1 |pages=35–42 | issn = 1078-8956| pmid = 15608650 |doi = 10.1038/nm1163 | bibcode = | oclc =| id = | url = http://doc.rero.ch/record/4324/files/1_albrecht_cgp.pdf| language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote =
|last=Kathiresan |author2=Willer |author3=Peloso |author4=Demissie |display-authors=etal |date=December 2008 |title=Common variants at 30 loci contribute to polygenic dyslipidemia |journal=Nat. Genet. |volume=41 |issue=1 |pages=56–65 | issn = | pmid = 19060906 |doi = 10.1038/ng.291 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = | first1 = S | pmc = 2881676
|last=McKay |first=James D |author2=Hung Rayjean J |display-authors=etal |date=December 2008 |title=Lung cancer susceptibility locus at 5p15.33 |journal=Nat. Genet. |volume=40 |issue=12 |pages=1404–6 | issn = | pmid = 18978790 |doi = 10.1038/ng.254 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = | pmc = 2748187
|last=Barrett |first=Jeffrey C |author2=Hansoul Sarah |display-authors=etal |date=August 2008 |title=Genome-wide association defines more than thirty distinct susceptibility loci for Crohn's disease |journal=Nat. Genet. |volume=40 |issue=8 |pages=955–62 | issn = | pmid = 18587394 |doi = 10.1038/ng.175 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = | pmc = 2574810
|collaboration=The STAR Consortium |author=Saar Kathrin |date=May 2008 |title=SNP and haplotype mapping for genetic analysis in the rat |journal=Nat. Genet. |volume=40 |issue=5 |pages=560–6 | issn = | pmid = 18443594 |pmc=5915293 |doi = 10.1038/ng.124 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote =
|last=Willer |first=Cristen J |authorlink= |date=February 2008 |title=Newly identified loci that influence lipid concentrations and risk of coronary artery disease |journal=Nat. Genet. |volume=40 |issue=2 |pages=161–9 | issn = | pmid = 18193043 |doi = 10.1038/ng.76 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = | last2 = Sanna | first2 = S | last3 = Jackson | first3 = AU | last4 = Scuteri | first4 = A | last5 = Bonnycastle | first5 = LL | last6 = Clarke | first6 = R | last7 = Heath | first7 = SC | last8 = Timpson | first8 = NJ | last9 = Najjar | first9 = SS |last10=Stringham |first10=Heather M |last11=Strait |first11=James |last12=Duren |first12=William L |last13=Maschio |first13=Andrea |last14=Busonero |first14=Fabio |last15=Mulas |first15=Antonella |last16=Albai |first16=Giuseppe |last17=Swift |first17=Amy J |last18=Morken |first18=Mario A |last19=Narisu |first19=Narisu |last20=Bennett |first20=Derrick |last21=Parish |first21=Sarah |last22=Shen |first22=Haiqing |last23=Galan |first23=Pilar |last24=Meneton |first24=Pierre |last25=Hercberg |first25=Serge |last26=Zelenika |first26=Diana |last27=Chen |first27=Wei-Min |last28=Li |first28=Yun |last29=Scott |first29=Laura J |last30=Scheet |first30=Paul A |display-authors=8 |pmc=5206900 }}
|authorlink= |date=November 2007 |title=Association scan of 14,500 nsSNPs in four common diseases identifies variants involved in autoimmunity |journal=Nat. Genet. |volume=39 |issue=11 |pages=1329–37 | issn = | pmid = 17952073 |doi = 10.1038/ng.2007.17 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = | author1 = Wellcome Trust Case Control Consortium | author2 = Australo-Anglo-American Spondylitis Consortium (TASC) | last3 = Burton | first3 = PR | last4 = Clayton | first4 = DG | last5 = Cardon | first5 = LR | last6 = Craddock | first6 = N | last7 = Deloukas | first7 = P | last8 = Duncanson | first8 = A | last9 = Kwiatkowski | first9 = DP |last10= Samani|first10= Nilesh J|last11= Todd|first11= John A|last12= Donnelly (Chair)|first12= Peter|last13= Barrett|first13= Jeffrey C|last14= Burton|first14= Paul R|last15= Davison|first15= Dan|last16= Donnelly|first16= Peter|last17= Easton|first17= Doug|last18= Evans|first18= David M|last19= Leung|first19= Hin-Tak|last20= Marchini|first20= Jonathan L|last21= Morris|first21= Andrew P|last22= Spencer|first22= Chris CA|last23= Tobin|first23= Martin D|last24= Cardon|first24= Lon R|last25= Clayton|first25= David G|last26= Attwood|first26= Antony P|last27= Boorman|first27= James P|last28= Cant|first28= Barbara|last29= Everson|first29= Ursula|last30= Hussey|first30= Judith M| pmc = 2680141 |display-authors= 8}}
|last=Dixon |first=Anna L |author2=Liang Liming |author3=Moffatt Miriam F |author4=Chen Wei |author5=Heath Simon |author6=Wong Kenny C C |author7=Taylor Jenny |author8=Burnett Edward |author9=Gut Ivo |author10=Farrall Martin |author11=Lathrop G Mark |author12=Abecasis Gonçalo R |author13=Cookson William O C |date=October 2007 |title=A genome-wide association study of global gene expression |journal=Nat. Genet. |volume=39 |issue=10 |pages=1202–7 | issn = | pmid = 17873877 |doi = 10.1038/ng2109 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote =
|last=Menzel |first=Stephan |author2=Garner Chad |author3=Gut Ivo |author4=Matsuda Fumihiko |author5=Yamaguchi Masao |author6=Heath Simon |author7=Foglio Mario |author8=Zelenika Diana |author9=Boland Anne |author10=Rooks Helen |author11=Best Steve |author12=Spector Tim D |author13=Farrall Martin |author14=Lathrop Mark |author15=Thein Swee Lay |date=October 2007 |title=A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15 |journal=Nat. Genet. |volume=39 |issue=10 |pages=1197–9 | issn = | pmid = 17767159 |doi = 10.1038/ng2108 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote =
|last=Fischer |first=Judith |authorlink= |author2=Lefèvre Caroline |author3=Morava Eva |author4=Mussini Jean-Marie |author5=Laforêt Pascal |author6=Negre-Salvayre Anne |author7=Lathrop Mark |author8=Salvayre Robert |date=January 2007 |title=The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy |journal=Nat. Genet. |volume=39 |issue=1 |pages=28–30 | issn = 1061-4036| pmid = 17187067 |doi = 10.1038/ng1951 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote =
|last=Delmaghani |first=Sedigheh |author2=del Castillo Francisco J |author3=Michel Vincent |author4=Leibovici Michel |author5=Aghaie Asadollah |author6=Ron Uri |author7=Van Laer Lut |author8=Ben-Tal Nir |author9=Van Camp Guy |author10=Weil Dominique |author11=Langa Francina |author12=Lathrop Mark |author13=Avan Paul |author14=Petit Christine |date=July 2006 |title=Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy |journal=Nat. Genet. |volume=38 |issue=7 |pages=770–8 | issn = 1061-4036| pmid = 16804542 |doi = 10.1038/ng1829 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote =
|last=Sakuntabhai |first=Anavaj |authorlink=Julier Cécile |date=May 2005 |title=A variant in the CD209 promoter is associated with severity of dengue disease |journal=Nat. Genet. |volume=37 |issue=5 |pages=507–13 | issn = 1061-4036| pmid = 15838506 |doi = 10.1038/ng1550 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = | last2 = Turbpaiboon | first2 = C | last3 = Casadémont | first3 = I | last4 = Chuansumrit | first4 = A | last5 = Lowhnoo | first5 = T | last6 = Kajaste-Rudnitski | first6 = A | last7 = Kalayanarooj | first7 = SM | last8 = Tangnararatchakit | first8 = K | last9 = Tangthawornchaikul | first9 = N |last10=Vasanawathana |first10=Sirijit |last11=Chaiyaratana |first11=Wathanee |last12=Yenchitsomanus |first12=Pa-Thai |last13=Suriyaphol |first13=Prapat |last14=Avirutnan |first14=Panisadee |last15=Chokephaibulkit |first15=Kulkanya |last16=Matsuda |first16=Fumihiko |last17=Yoksan |first17=Sutee |last18=Jacob |first18=Yves |last19=Lathrop |first19=G Mark |last20=Malasit |first20=Prida |last21=Desprès |first21=Philippe |last22=Julier |first22=Cécile |display-authors=8 }}
|last=Auwerx |first=Johan |authorlink= |date=September 2004 |title=The European dimension for the mouse genome mutagenesis program |journal=Nat. Genet. |volume=36 |issue=9 |pages=925–7 | issn = 1061-4036| pmid = 15340424 |doi = 10.1038/ng0904-925 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = | last2 = Avner | first2 = P | last3 = Baldock | first3 = R | last4 = Ballabio | first4 = A | last5 = Balling | first5 = R | last6 = Barbacid | first6 = M | last7 = Berns | first7 = A | last8 = Bradley | first8 = A | last9 = Brown | first9 = S |last10=Carmeliet |first10=Peter |last11=Chambon |first11=Pierre |last12=Cox |first12=Roger |last13=Davidson |first13=Duncan |last14=Davies |first14=Kay |last15=Duboule |first15=Denis |last16=Forejt |first16=Jiri |last17=Granucci |first17=Francesca |last18=Hastie |first18=Nick |last19=De Angelis |first19=Martin Hrabé |last20=Jackson |first20=Ian |last21=Kioussis |first21=Dimitris |last22=Kollias |first22=George |last23=Lathrop |first23=Mark |last24=Lendahl |first24=Urban |last25=Malumbres |first25=Marcos |last26=von Melchner |first26=Harald |last27=Müller |first27=Werner |last28=Partanen |first28=Juha |last29=Ricciardi-Castagnoli |first29=Paola |last30=Rigby |first30=Peter | pmc = 2716028 |display-authors=8 }}
|last=Gut |first=Ivo G |authorlink= |author2=Lathrop G Mark |date=August 2004 |title=Duplicating SNPs |journal=Nat. Genet. |volume=36 |issue=8 |pages=789–90 | issn = 1061-4036| pmid = 15284844 |doi = 10.1038/ng0804-789 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote =
|last=Allen |first=Maxine |author2=Heinzmann Andrea |author3=Noguchi Emiko |author4=Abecasis Gonçalo |author5=Broxholme John |author6=Ponting Chris P |author7=Bhattacharyya Sumit |author8=Tinsley Jon |author9=Zhang Youming |author10=Holt Richard |author11=Jones E Yvonne |author12=Lench Nick |author13=Carey Alisoun |author14=Jones Helene |author15=Dickens Nicholas J |author16=Dimon Claire |author17=Nicholls Rosie |author18=Baker Crystal |author19=Xue Luzheng |author20=Townsend Elizabeth |author21=Kabesch Michael |author22=Weiland Stephan K |author23=Carr David |author24=von Mutius Erika |author25=Adcock Ian M |author26=Barnes Peter J |author27=Lathrop G Mark |author28=Edwards Mark |author29=Moffatt Miriam F |author30=Cookson William O C M |date=November 2003 |title=Positional cloning of a novel gene influencing asthma from chromosome 2q14 |journal=Nat. Genet. |volume=35 |issue=3 |pages=258–63 | issn = 1061-4036| pmid = 14566338 |doi = 10.1038/ng1256 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote =
|last=Caulfield |first=Mark |author2=Munroe Patricia |author3=Pembroke Janine |author4=Samani Nilesh |author5=Dominiczak Anna |author6=Brown Morris |author7=Benjamin Nigel |author8=Webster John |author9=Ratcliffe Peter |author10=O'Shea Suzanne |author11=Papp Jeanette |author12=Taylor Elizabeth |author13=Dobson Richard |author14=Knight Joanne |author15=Newhouse Stephen |author16=Hooper Joel |author17=Lee Wai |author18=Brain Nick |author19=Clayton David |author20=Lathrop G Mark |author21=Farrall Martin |author22=Connell John |date=June 2003 |title=Genome-wide mapping of human loci for essential hypertension |journal=Lancet |volume=361 |issue=9375 |pages=2118–23 | issn = | pmid = 12826435 |doi = 10.1016/S0140-6736(03)13722-1 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = References1. ^{{cite web | url=http://publications.mcgill.ca/reporter/2011/02/lathrop-takes-helm-of-genome-innovation-centre/| title=Lathrop takes helm of genome Innovation Centre|accessdate=2012-12-21}} {{Authority control}}{{DEFAULTSORT:Lathrop, Mark}} 8 : Biostatisticians|Canadian scientists|Living people|1950 births|McGill University faculty|University of Washington alumni|People associated with the University of Oxford|Canadian geneticists |
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