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성함이나 학술지명, PMID로 찾아보십시오.
Feenstra B에 대해
35건, 그중 15건 표시.
Genetic effects on the timing of parturition and links to fetal birth weight
Solé-Navais P,
Flatley C,
Steinthorsdottir V,
Vaudel M,
Juodakis J,
Chen J,
Laisk T,
LaBella AL,
Westergaard D,
Bacelis J,
Brumpton B,
Skotte L
외 73명 — 모두 보기
Borges MC,
Helgeland Ø,
Mahajan A,
Wielscher M,
Lin F,
Briggs C,
Wang CA,
Moen GH,
Beaumont RN,
Bradfield JP,
Abraham A,
Thorleifsson G,
Gabrielsen ME,
Ostrowski SR,
Modzelewska D,
Nohr EA,
Hypponen E,
Srivastava A,
Talbot O,
Allard C,
Williams SM,
Menon R,
Shields BM,
Sveinbjornsson G,
Xu H,
Melbye M,
Lowe W Jr,
Bouchard L,
Oken E,
Pedersen OB,
Gudbjartsson DF,
Erikstrup C,
Sørensen E,
Lie RT,
Teramo K,
Hallman M,
Juliusdottir T,
Hakonarson H,
Ullum H,
Hattersley AT,
Sletner L,
Merialdi M,
Rifas-Shiman SL,
Steingrimsdottir T,
Scholtens D,
Power C,
West J,
Nyegaard M,
Capra JA,
Skogholt AH,
Magnus P,
Andreassen OA,
Thorsteinsdottir U,
Grant SFA,
Qvigstad E,
Pennell CE,
Hivert MF,
Hayes GM,
Jarvelin MR,
McCarthy MI,
Lawlor DA,
Nielsen HS,
Mägi R,
Rokas A,
Hveem K,
Stefansson K,
Feenstra B,
Njolstad P,
Muglia LJ,
Freathy RM,
Johansson S,
Zhang G,
Jacobsson B
Early Growth Genetics Consortium · Estonian Biobank Research Team 외 컨소시엄 1곳
Nature genetics · 2023 · PMID 37012456 · open access
페이지 4개
Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes
Ruth KS,
Campbell PJ,
Chew S,
Lim EM,
Hadlow N,
Stuckey BG,
Brown SJ,
Feenstra B,
Joseph J,
Surdulescu GL,
Zheng HF,
Richards JB
외 4명 — 모두 보기
European journal of human genetics : EJHG · 2016 · PMID 26014426 · open access
페이지 3개
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus
Fadista J,
Lund M,
Skotte L,
Geller F,
Nandakumar P,
Chatterjee S,
Matsson H,
Granström AL,
Wester T,
Salo P,
Virtanen V,
Carstensen L
외 8명 — 모두 보기
European journal of human genetics : EJHG · 2018 · PMID 29379196
페이지 3개
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis
Fadista J,
Skotte L,
Geller F,
Bybjerg-Grauholm J,
Gørtz S,
Romitti PA,
Caggana M,
Kay DM,
Matsson H,
Boyd HA,
Hougaard DM,
Nordenskjöld A
외 3명 — 모두 보기
Human molecular genetics · 2019 · PMID 30281099 · open access
페이지 3개
Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci
Pasanen A,
Karjalainen MK,
Zhang G,
Tiensuu H,
Haapalainen AM,
Ojaniemi M,
Feenstra B,
Jacobsson B,
Palotie A,
Laivuori H,
Muglia LJ,
Rämet M
외 1명 — 모두 보기
FinnGen
PLoS genetics · 2023 · PMID 37871108 · open access
페이지 3개
Genome-wide association study identifies four loci associated with eruption of permanent teeth
Geller F,
Feenstra B,
Zhang H,
Shaffer JR,
Hansen T,
Esserlind AL,
Boyd HA,
Nohr EA,
Timpson NJ,
Fatemifar G,
Paternoster L,
Evans DM
외 10명 — 모두 보기
PLoS genetics · 2011 · PMID 21931568 · open access
페이지 2개
A novel common variant in DCST2 is associated with length in early life and height in adulthood
van der Valk RJ,
Kreiner-Møller E,
Kooijman MN,
Guxens M,
Stergiakouli E,
Sääf A,
Bradfield JP,
Geller F,
Hayes MG,
Cousminer DL,
Körner A,
Thiering E
외 105명 — 모두 보기
Curtin JA,
Myhre R,
Huikari V,
Joro R,
Kerkhof M,
Warrington NM,
Pitkänen N,
Ntalla I,
Horikoshi M,
Veijola R,
Freathy RM,
Teo YY,
Barton SJ,
Evans DM,
Kemp JP,
St Pourcain B,
Ring SM,
Davey Smith G,
Bergström A,
Kull I,
Hakonarson H,
Mentch FD,
Bisgaard H,
Chawes B,
Stokholm J,
Waage J,
Eriksen P,
Sevelsted A,
Melbye M,
van Duijn CM,
Medina-Gomez C,
Hofman A,
de Jongste JC,
Taal HR,
Uitterlinden AG,
Armstrong LL,
Eriksson J,
Palotie A,
Bustamante M,
Estivill X,
Gonzalez JR,
Llop S,
Kiess W,
Mahajan A,
Flexeder C,
Tiesler CM,
Murray CS,
Simpson A,
Magnus P,
Sengpiel V,
Hartikainen AL,
Keinanen-Kiukaanniemi S,
Lewin A,
Da Silva Couto Alves A,
Blakemore AI,
Buxton JL,
Kaakinen M,
Rodriguez A,
Sebert S,
Vaarasmaki M,
Lakka T,
Lindi V,
Gehring U,
Postma DS,
Ang W,
Newnham JP,
Lyytikäinen LP,
Pahkala K,
Raitakari OT,
Panoutsopoulou K,
Zeggini E,
Boomsma DI,
Groen-Blokhuis M,
Ilonen J,
Franke L,
Hirschhorn JN,
Pers TH,
Liang L,
Huang J,
Hocher B,
Knip M,
Saw SM,
Holloway JW,
Melén E,
Grant SF,
Feenstra B,
Lowe WL,
Widén E,
Sergeyev E,
Grallert H,
Custovic A,
Jacobsson B,
Jarvelin MR,
Atalay M,
Koppelman GH,
Pennell CE,
Niinikoski H,
Dedoussis GV,
Mccarthy MI,
Frayling TM,
Sunyer J,
Timpson NJ,
Rivadeneira F,
Bønnelykke K,
Jaddoe VW
Early Genetics and Lifecourse Epidemiology (EAGLE) Consortium · Genetic Investigation of ANthropometric Traits (GIANT) Consortium 외 컨소시엄 1곳
Human molecular genetics · 2015 · PMID 25281659 · open access
페이지 2개
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
Cornelis MC,
Byrne EM,
Esko T,
Nalls MA,
Ganna A,
Paynter N,
Monda KL,
Amin N,
Fischer K,
Renstrom F,
Ngwa JS,
Huikari V
외 142명 — 모두 보기
Cavadino A,
Nolte IM,
Teumer A,
Yu K,
Marques-Vidal P,
Rawal R,
Manichaikul A,
Wojczynski MK,
Vink JM,
Zhao JH,
Burlutsky G,
Lahti J,
Mikkilä V,
Lemaitre RN,
Eriksson J,
Musani SK,
Tanaka T,
Geller F,
Luan J,
Hui J,
Mägi R,
Dimitriou M,
Garcia ME,
Ho WK,
Wright MJ,
Rose LM,
Magnusson PK,
Pedersen NL,
Couper D,
Oostra BA,
Hofman A,
Ikram MA,
Tiemeier HW,
Uitterlinden AG,
van Rooij FJ,
Barroso I,
Johansson I,
Xue L,
Kaakinen M,
Milani L,
Power C,
Snieder H,
Stolk RP,
Baumeister SE,
Biffar R,
Gu F,
Bastardot F,
Kutalik Z,
Jacobs DR Jr,
Forouhi NG,
Mihailov E,
Lind L,
Lindgren C,
Michaëlsson K,
Morris A,
Jensen M,
Khaw KT,
Luben RN,
Wang JJ,
Männistö S,
Perälä MM,
Kähönen M,
Lehtimäki T,
Viikari J,
Mozaffarian D,
Mukamal K,
Psaty BM,
Döring A,
Heath AC,
Montgomery GW,
Dahmen N,
Carithers T,
Tucker KL,
Ferrucci L,
Boyd HA,
Melbye M,
Treur JL,
Mellström D,
Hottenga JJ,
Prokopenko I,
Tönjes A,
Deloukas P,
Kanoni S,
Lorentzon M,
Houston DK,
Liu Y,
Danesh J,
Rasheed A,
Mason MA,
Zonderman AB,
Franke L,
Kristal BS,
Karjalainen J,
Reed DR,
Westra HJ,
Evans MK,
Saleheen D,
Harris TB,
Dedoussis G,
Curhan G,
Stumvoll M,
Beilby J,
Pasquale LR,
Feenstra B,
Bandinelli S,
Ordovas JM,
Chan AT,
Peters U,
Ohlsson C,
Gieger C,
Martin NG,
Waldenberger M,
Siscovick DS,
Raitakari O,
Eriksson JG,
Mitchell P,
Hunter DJ,
Kraft P,
Rimm EB,
Boomsma DI,
Borecki IB,
Loos RJ,
Wareham NJ,
Vollenweider P,
Caporaso N,
Grabe HJ,
Neuhouser ML,
Wolffenbuttel BH,
Hu FB,
Hyppönen E,
Järvelin MR,
Cupples LA,
Franks PW,
Ridker PM,
van Duijn CM,
Heiss G,
Metspalu A,
North KE,
Ingelsson E,
Nettleton JA,
van Dam RM,
Chasman DI
Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) 외 컨소시엄 2곳
Molecular psychiatry · 2015 · PMID 25288136
페이지 2개
Genetic studies of body mass index yield new insights for obesity biology
Locke AE,
Kahali B,
Berndt SI,
Justice AE,
Pers TH,
Day FR,
Powell C,
Vedantam S,
Buchkovich ML,
Yang J,
Croteau-Chonka DC,
Esko T
외 470명 — 모두 보기
Fall T,
Ferreira T,
Gustafsson S,
Kutalik Z,
Luan J,
Mägi R,
Randall JC,
Winkler TW,
Wood AR,
Workalemahu T,
Faul JD,
Smith JA,
Zhao JH,
Zhao W,
Chen J,
Fehrmann R,
Hedman ÅK,
Karjalainen J,
Schmidt EM,
Absher D,
Amin N,
Anderson D,
Beekman M,
Bolton JL,
Bragg-Gresham JL,
Buyske S,
Demirkan A,
Deng G,
Ehret GB,
Feenstra B,
Feitosa MF,
Fischer K,
Goel A,
Gong J,
Jackson AU,
Kanoni S,
Kleber ME,
Kristiansson K,
Lim U,
Lotay V,
Mangino M,
Leach IM,
Medina-Gomez C,
Medland SE,
Nalls MA,
Palmer CD,
Pasko D,
Pechlivanis S,
Peters MJ,
Prokopenko I,
Shungin D,
Stančáková A,
Strawbridge RJ,
Sung YJ,
Tanaka T,
Teumer A,
Trompet S,
van der Laan SW,
van Setten J,
Van Vliet-Ostaptchouk JV,
Wang Z,
Yengo L,
Zhang W,
Isaacs A,
Albrecht E,
Ärnlöv J,
Arscott GM,
Attwood AP,
Bandinelli S,
Barrett A,
Bas IN,
Bellis C,
Bennett AJ,
Berne C,
Blagieva R,
Blüher M,
Böhringer S,
Bonnycastle LL,
Böttcher Y,
Boyd HA,
Bruinenberg M,
Caspersen IH,
Chen YI,
Clarke R,
Daw EW,
de Craen AJM,
Delgado G,
Dimitriou M,
Doney ASF,
Eklund N,
Estrada K,
Eury E,
Folkersen L,
Fraser RM,
Garcia ME,
Geller F,
Giedraitis V,
Gigante B,
Go AS,
Golay A,
Goodall AH,
Gordon SD,
Gorski M,
Grabe HJ,
Grallert H,
Grammer TB,
Gräßler J,
Grönberg H,
Groves CJ,
Gusto G,
Haessler J,
Hall P,
Haller T,
Hallmans G,
Hartman CA,
Hassinen M,
Hayward C,
Heard-Costa NL,
Helmer Q,
Hengstenberg C,
Holmen O,
Hottenga JJ,
James AL,
Jeff JM,
Johansson Å,
Jolley J,
Juliusdottir T,
Kinnunen L,
Koenig W,
Koskenvuo M,
Kratzer W,
Laitinen J,
Lamina C,
Leander K,
Lee NR,
Lichtner P,
Lind L,
Lindström J,
Lo KS,
Lobbens S,
Lorbeer R,
Lu Y,
Mach F,
Magnusson PKE,
Mahajan A,
McArdle WL,
McLachlan S,
Menni C,
Merger S,
Mihailov E,
Milani L,
Moayyeri A,
Monda KL,
Morken MA,
Mulas A,
Müller G,
Müller-Nurasyid M,
Musk AW,
Nagaraja R,
Nöthen MM,
Nolte IM,
Pilz S,
Rayner NW,
Renstrom F,
Rettig R,
Ried JS,
Ripke S,
Robertson NR,
Rose LM,
Sanna S,
Scharnagl H,
Scholtens S,
Schumacher FR,
Scott WR,
Seufferlein T,
Shi J,
Smith AV,
Smolonska J,
Stanton AV,
Steinthorsdottir V,
Stirrups K,
Stringham HM,
Sundström J,
Swertz MA,
Swift AJ,
Syvänen AC,
Tan ST,
Tayo BO,
Thorand B,
Thorleifsson G,
Tyrer JP,
Uh HW,
Vandenput L,
Verhulst FC,
Vermeulen SH,
Verweij N,
Vonk JM,
Waite LL,
Warren HR,
Waterworth D,
Weedon MN,
Wilkens LR,
Willenborg C,
Wilsgaard T,
Wojczynski MK,
Wong A,
Wright AF,
Zhang Q,
Brennan EP,
Choi M,
Dastani Z,
Drong AW,
Eriksson P,
Franco-Cereceda A,
Gådin JR,
Gharavi AG,
Goddard ME,
Handsaker RE,
Huang J,
Karpe F,
Kathiresan S,
Keildson S,
Kiryluk K,
Kubo M,
Lee JY,
Liang L,
Lifton RP,
Ma B,
McCarroll SA,
McKnight AJ,
Min JL,
Moffatt MF,
Montgomery GW,
Murabito JM,
Nicholson G,
Nyholt DR,
Okada Y,
Perry JRB,
Dorajoo R,
Reinmaa E,
Salem RM,
Sandholm N,
Scott RA,
Stolk L,
Takahashi A,
Tanaka T,
van 't Hooft FM,
Vinkhuyzen AAE,
Westra HJ,
Zheng W,
Zondervan KT,
Heath AC,
Arveiler D,
Bakker SJL,
Beilby J,
Bergman RN,
Blangero J,
Bovet P,
Campbell H,
Caulfield MJ,
Cesana G,
Chakravarti A,
Chasman DI,
Chines PS,
Collins FS,
Crawford DC,
Cupples LA,
Cusi D,
Danesh J,
de Faire U,
den Ruijter HM,
Dominiczak AF,
Erbel R,
Erdmann J,
Eriksson JG,
Farrall M,
Felix SB,
Ferrannini E,
Ferrières J,
Ford I,
Forouhi NG,
Forrester T,
Franco OH,
Gansevoort RT,
Gejman PV,
Gieger C,
Gottesman O,
Gudnason V,
Gyllensten U,
Hall AS,
Harris TB,
Hattersley AT,
Hicks AA,
Hindorff LA,
Hingorani AD,
Hofman A,
Homuth G,
Hovingh GK,
Humphries SE,
Hunt SC,
Hyppönen E,
Illig T,
Jacobs KB,
Jarvelin MR,
Jöckel KH,
Johansen B,
Jousilahti P,
Jukema JW,
Jula AM,
Kaprio J,
Kastelein JJP,
Keinanen-Kiukaanniemi SM,
Kiemeney LA,
Knekt P,
Kooner JS,
Kooperberg C,
Kovacs P,
Kraja AT,
Kumari M,
Kuusisto J,
Lakka TA,
Langenberg C,
Marchand LL,
Lehtimäki T,
Lyssenko V,
Männistö S,
Marette A,
Matise TC,
McKenzie CA,
McKnight B,
Moll FL,
Morris AD,
Morris AP,
Murray JC,
Nelis M,
Ohlsson C,
Oldehinkel AJ,
Ong KK,
Madden PAF,
Pasterkamp G,
Peden JF,
Peters A,
Postma DS,
Pramstaller PP,
Price JF,
Qi L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Ridker PM,
Rioux JD,
Ritchie MD,
Rudan I,
Salomaa V,
Samani NJ,
Saramies J,
Sarzynski MA,
Schunkert H,
Schwarz PEH,
Sever P,
Shuldiner AR,
Sinisalo J,
Stolk RP,
Strauch K,
Tönjes A,
Trégouët DA,
Tremblay A,
Tremoli E,
Virtamo J,
Vohl MC,
Völker U,
Waeber G,
Willemsen G,
Witteman JC,
Zillikens MC,
Adair LS,
Amouyel P,
Asselbergs FW,
Assimes TL,
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Boehm BO,
Boerwinkle E,
Bornstein SR,
Bottinger EP,
Bouchard C,
Cauchi S,
Chambers JC,
Chanock SJ,
Cooper RS,
de Bakker PIW,
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Ferrucci L,
Franks PW,
Froguel P,
Groop LC,
Haiman CA,
Hamsten A,
Hui J,
Hunter DJ,
Hveem K,
Kaplan RC,
Kivimaki M,
Kuh D,
Laakso M,
Liu Y,
Martin NG,
März W,
Melbye M,
Metspalu A,
Moebus S,
Munroe PB,
Njølstad I,
Oostra BA,
Palmer CNA,
Pedersen NL,
Perola M,
Pérusse L,
Peters U,
Power C,
Quertermous T,
Rauramaa R,
Rivadeneira F,
Saaristo TE,
Saleheen D,
Sattar N,
Schadt EE,
Schlessinger D,
Slagboom PE,
Snieder H,
Spector TD,
Thorsteinsdottir U,
Stumvoll M,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
van der Harst P,
Walker M,
Wallaschofski H,
Wareham NJ,
Watkins H,
Weir DR,
Wichmann HE,
Wilson JF,
Zanen P,
Borecki IB,
Deloukas P,
Fox CS,
Heid IM,
O'Connell JR,
Strachan DP,
Stefansson K,
van Duijn CM,
Abecasis GR,
Franke L,
Frayling TM,
McCarthy MI,
Visscher PM,
Scherag A,
Willer CJ,
Boehnke M,
Mohlke KL,
Lindgren CM,
Beckmann JS,
Barroso I,
North KE,
Ingelsson E,
Hirschhorn JN,
Loos RJF,
Speliotes EK
LifeLines Cohort Study · ADIPOGen Consortium 외 컨소시엄 12곳
Nature · 2015 · PMID 25673413
페이지 2개
Genetic Associations with Gestational Duration and Spontaneous Preterm Birth
Zhang G,
Feenstra B,
Bacelis J,
Liu X,
Muglia LM,
Juodakis J,
Miller DE,
Litterman N,
Jiang PP,
Russell L,
Hinds DA,
Hu Y
외 26명 — 모두 보기
Weirauch MT,
Chen X,
Chavan AR,
Wagner GP,
Pavličev M,
Nnamani MC,
Maziarz J,
Karjalainen MK,
Rämet M,
Sengpiel V,
Geller F,
Boyd HA,
Palotie A,
Momany A,
Bedell B,
Ryckman KK,
Huusko JM,
Forney CR,
Kottyan LC,
Hallman M,
Teramo K,
Nohr EA,
Davey Smith G,
Melbye M,
Jacobsson B,
Muglia LJ
The New England journal of medicine · 2017 · PMID 28877031 · open access
페이지 2개
Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism
Solé-Navais P,
Juodakis J,
Ytterberg K,
Wu X,
Bradfield JP,
Vaudel M,
LaBella AL,
Helgeland Ø,
Flatley C,
Geller F,
Finel M,
Zhao M
외 11명 — 모두 보기
Lazarus P,
Hakonarson H,
Magnus P,
Andreassen OA,
Njølstad PR,
Grant SFA,
Feenstra B,
Muglia LJ,
Johansson S,
Zhang G,
Jacobsson B
Nature communications · 2024 · PMID 39214992 · open access
페이지 2개
Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption
Sulem P,
Gudbjartsson DF,
Geller F,
Prokopenko I,
Feenstra B,
Aben KK,
Franke B,
den Heijer M,
Kovacs P,
Stumvoll M,
Mägi R,
Yanek LR
외 18명 — 모두 보기
Becker LC,
Boyd HA,
Stacey SN,
Walters GB,
Jonasdottir A,
Thorleifsson G,
Holm H,
Gudjonsson SA,
Rafnar T,
Björnsdottir G,
Becker DM,
Melbye M,
Kong A,
Tönjes A,
Thorgeirsson T,
Thorsteinsdottir U,
Kiemeney LA,
Stefansson K
Human molecular genetics · 2011 · PMID 21357676
페이지 1개
Common variants at 12q15 and 12q24 are associated with infant head circumference
Taal HR,
Pourcain BS,
Thiering E,
Das S,
Mook-Kanamori DO,
Warrington NM,
Kaakinen M,
Kreiner-Møller E,
Bradfield JP,
Freathy RM,
Geller F,
Guxens M
외 74명 — 모두 보기
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