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词条 Mark Lathrop
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  1. Bibliography

  2. References

{{Infobox scientist
|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

  • {{cite journal

|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
  • {{cite journal

|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 =
  • {{cite journal

|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 =
  • {{cite journal

|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 =
  • {{cite journal

|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
  • {{cite journal

|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
  • {{cite journal

|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
  • {{cite journal

|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 =
  • {{cite journal

|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
}}
  • {{cite journal

|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}}
  • {{cite journal

|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 =
  • {{cite journal

|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 =
  • {{cite journal

|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 =
  • {{cite journal

|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 =
  • {{cite journal

|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
}}
  • {{cite journal

|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
}}
  • {{cite journal

|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 =
  • {{cite journal

|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 =
  • {{cite journal

|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 =

References

1. ^{{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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