Works by Feenstra, Bjarke

Results: 49
    1

    Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype-based genetic score analysis in 10,734 mother-infant pairs.

    Published in:
    2020
    By:
    • Chen, Jing;
    • Bacelis, Jonas;
    • Sole-Navais, Pol;
    • Srivastava, Amit;
    • Juodakis, Julius;
    • Rouse, Amy;
    • Hallman, Mikko;
    • Teramo, Kari;
    • Melbye, Mads;
    • Feenstra, Bjarke;
    • Freathy, Rachel M.;
    • Smith, George Davey;
    • Lawlor, Deborah A.;
    • Murray, Jeffrey C.;
    • Williams, Scott M.;
    • Jacobsson, Bo;
    • Muglia, Louis J.;
    • Zhang, Ge
    Publication type:
    journal article
    2

    The gene, environment association studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions.

    Published in:
    Genetic Epidemiology, 2010, v. 34, n. 4, p. 364, doi. 10.1002/gepi.20492
    By:
    • Cornelis, Marilyn C.;
    • Agrawal, Arpana;
    • Cole, John W.;
    • Hansel, Nadia N.;
    • Barnes, Kathleen C.;
    • Beaty, Terri H.;
    • Bennett, Siiri N.;
    • Bierut, Laura J.;
    • Boerwinkle, Eric;
    • Doheny, Kimberly F.;
    • Feenstra, Bjarke;
    • Feingold, Eleanor;
    • Fornage, Myriam;
    • Haiman, Christopher A.;
    • Harris, Emily L.;
    • Hayes, M. Geoffrey;
    • Heit, John A.;
    • Hu, Frank B.;
    • Kang, Jae H.;
    • Laurie, Cathy C.
    Publication type:
    Article
    3

    Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism.

    Published in:
    Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-51947-w
    By:
    • Solé-Navais, Pol;
    • Juodakis, Julius;
    • Ytterberg, Karin;
    • Wu, Xiaoping;
    • Bradfield, Jonathan P.;
    • Vaudel, Marc;
    • LaBella, Abigail L.;
    • Helgeland, Øyvind;
    • Flatley, Christopher;
    • Geller, Frank;
    • Finel, Moshe;
    • Zhao, Mengqi;
    • Lazarus, Philip;
    • Hakonarson, Hakon;
    • Magnus, Per;
    • Andreassen, Ole A.;
    • Njølstad, Pål R.;
    • Grant, Struan F. A.;
    • Feenstra, Bjarke;
    • Muglia, Louis J.
    Publication type:
    Article
    4
    5

    Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30921-4
    By:
    • Fadista, João;
    • Skotte, Line;
    • Karjalainen, Juha;
    • Abner, Erik;
    • Sørensen, Erik;
    • Ullum, Henrik;
    • Werge, Thomas;
    • iPSYCH Group;
    • Hougaard, David M.;
    • Børglum, Anders D.;
    • Nordentoft, Merete;
    • Mortensen, Preben B.;
    • Esko, Tõnu;
    • Milani, Lili;
    • Palotie, Aarno;
    • Daly, Mark;
    • Melbye, Mads;
    • Feenstra, Bjarke;
    • Geller, Frank
    Publication type:
    Article
    6
    7
    8

    Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis.

    Published in:
    Nature Genetics, 2012, v. 44, n. 2, p. 187, doi. 10.1038/ng.1017
    By:
    • Paternoster, Lavinia;
    • Standl, Marie;
    • Chen, Chih-Mei;
    • Ramasamy, Adaikalavan;
    • Bønnelykke, Klaus;
    • Duijts, Liesbeth;
    • Ferreira, Manuel A;
    • Alves, Alexessander Couto;
    • Thyssen, Jacob P;
    • Albrecht, Eva;
    • Baurecht, Hansjörg;
    • Feenstra, Bjarke;
    • Sleiman, Patrick M A;
    • Hysi, Pirro;
    • Warrington, Nicole M;
    • Curjuric, Ivan;
    • Myhre, Ronny;
    • Curtin, John A;
    • Groen-Blokhuis, Maria M;
    • Kerkhof, Marjan
    Publication type:
    Article
    9

    Genome partitioning of genetic variation for complex traits using common SNPs.

    Published in:
    Nature Genetics, 2011, v. 43, n. 6, p. 519, doi. 10.1038/ng.823
    By:
    • Jian Yang;
    • Manolio, Teri A.;
    • Pasquale, Louis R.;
    • Boerwinkle, Eric;
    • Caporaso, Neil;
    • Cunningham, Julie M.;
    • de Andrade, Mariza;
    • Feenstra, Bjarke;
    • Feingold, Eleanor;
    • Hayes, M. Geoffrey;
    • Hill, William G.;
    • Landi, Maria Teresa;
    • Alonso, Alvaro;
    • Lettre, Guillaume;
    • Peng Lin;
    • Hua Ling;
    • Lowe, William;
    • Mathias, Rasika A.;
    • Melbye, Mads;
    • Pugh, Elizabeth
    Publication type:
    Article
    10

    Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.

    Published in:
    Nature Genetics, 2010, v. 42, n. 12, p. 1077, doi. 10.1038/ng.714
    By:
    • Elks, Cathy E.;
    • Perry, John R. B.;
    • Sulem, Patrick;
    • Chasman, Daniel I.;
    • Franceschini, Nora;
    • He, Chunyan;
    • Lunetta, Kathryn L.;
    • Visser, Jenny A.;
    • Byrne, Enda M.;
    • Cousminer, Diana L.;
    • Gudbjartsson, Daniel F.;
    • Esko, Tõnu;
    • Feenstra, Bjarke;
    • Hottenga, Jouke-Jan;
    • Koller, Daniel L.;
    • Kutalik, Zoltán;
    • Peng Lin;
    • Mangino, Massimo;
    • Marongiu, Mara;
    • McArdle, Patrick F.
    Publication type:
    Article
    11

    Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche.

    Published in:
    Nature Genetics, 2009, v. 41, n. 6, p. 734, doi. 10.1038/ng.383
    By:
    • Sulem, Patrick;
    • Gudbjartsson, Daniel F.;
    • Rafnar, Thorunn;
    • Holm, Hilma;
    • Olafsdottir, Elinborg J.;
    • Olafsdottir, Gudridur H.;
    • Jonsson, Thorvaldur;
    • Alexandersen, Peter;
    • Feenstra, Bjarke;
    • Boyd, Heather A.;
    • Aben, Katja K.;
    • Verbeek, Andre L. M.;
    • Roeleveld, Nel;
    • Jonasdottir, Aslaug;
    • Styrkarsdottir, Unnur;
    • Steinthorsdottir, Valgerdur;
    • Karason, Ari;
    • Stacey, Simon N.;
    • Gudmundsson, Julius;
    • Jakobsdottir, Margret
    Publication type:
    Article
    12

    Genome-Wide Association Study Identifies Four Loci Associated with Eruption of Permanent Teeth.

    Published in:
    PLoS Genetics, 2011, v. 7, n. 9, p. 1, doi. 10.1371/journal.pgen.1002275
    By:
    • Geller, Frank;
    • Feenstra, Bjarke;
    • Zhang, Hao;
    • Shaffer, John R.;
    • Hansen, Thomas;
    • Esserlind, Ann-Louise;
    • Boyd, Heather A.;
    • Nohr, Ellen A.;
    • Timpson, Nicholas J.;
    • Fatemifar, Ghazaleh;
    • Paternoster, Lavinia;
    • Evans, David M.;
    • Weyant, Robert J.;
    • Levy, Steven M.;
    • Lathrop, Mark;
    • Smith, George Davey;
    • Murray, Jeffrey C.;
    • Olesen, Jes;
    • Werge, Thomas;
    • Marazita, Mary L.
    Publication type:
    Article
    13

    Clonal hematopoiesis and COVID‐19 hospitalization in Danish adults.

    Published in:
    HemaSphere, 2024, v. 8, n. 3, p. 1, doi. 10.1002/hem3.58
    By:
    • Sequeros, Celia Burgos;
    • Tulstrup, Morten;
    • Bliddal, Sofie;
    • Sørensen, Karina Meden;
    • Nissen, Ioanna;
    • Rezahosseini, Omid;
    • Brooks, Patrick Terrence;
    • Feenstra, Bjarke;
    • Gang, Anne Ortved;
    • Geller, Frank;
    • Hald, Annemette;
    • Harboe, Zitta Barrella;
    • Helleberg, Marie;
    • Jespersen, Jakob S.;
    • Lebech, Anne‐Mette;
    • Lindegaard, Birgitte;
    • Mogensen, Trine H.;
    • Møller, Maria Elizabeth Engel;
    • Nielsen, Claus Henrik;
    • Niemann, Carsten Utoft
    Publication type:
    Article
    14

    Birth characteristics and risk of febrile seizures.

    Published in:
    Acta Neurologica Scandinavica, 2021, v. 144, n. 1, p. 51, doi. 10.1111/ane.13420
    By:
    • Christensen, Kirstine J.;
    • Dreier, Julie W.;
    • Skotte, Line;
    • Feenstra, Bjarke;
    • Grove, Jakob;
    • Børglum, Anders;
    • Mitrovic, Mitja;
    • Cotsapas, Chris;
    • Christensen, Jakob
    Publication type:
    Article
    15

    Association of Adiposity Genetic Variants With Menarche Timing in 92,105 Women of European Descent.

    Published in:
    2013
    By:
    • Fernández-Rhodes, Lindsay;
    • Demerath, Ellen W.;
    • Cousminer, Diana L.;
    • Tao, Ran;
    • Dreyfus, Jill G.;
    • Esko, Tõnu;
    • Smith, Albert V.;
    • Gudnason, Vilmundur;
    • Harris, Tamara B.;
    • Launer, Lenore;
    • McArdle, Patrick F.;
    • Yerges-Armstrong, Laura M.;
    • Elks, Cathy E.;
    • Strachan, David P.;
    • Kutalik, Zoltán;
    • Vollenweider, Peter;
    • Feenstra, Bjarke;
    • Boyd, Heather A.;
    • Metspalu, Andres;
    • Mihailov, Evelin
    Publication type:
    Journal Article
    16

    Association of Adiposity Genetic Variants With Menarche Timing in 92,105 Women of European Descent.

    Published in:
    American Journal of Epidemiology, 2013, v. 178, n. 3, p. 451, doi. 10.1093/aje/kws473
    By:
    • Fernández-Rhodes, Lindsay;
    • Demerath, Ellen W.;
    • Cousminer, Diana L.;
    • Tao, Ran;
    • Dreyfus, Jill G.;
    • Esko, Tõnu;
    • Smith, Albert V.;
    • Gudnason, Vilmundur;
    • Harris, Tamara B.;
    • Launer, Lenore;
    • McArdle, Patrick F.;
    • Yerges-Armstrong, Laura M.;
    • Elks, Cathy E.;
    • Strachan, David P.;
    • Kutalik, Zoltán;
    • Vollenweider, Peter;
    • Feenstra, Bjarke;
    • Boyd, Heather A.;
    • Metspalu, Andres;
    • Mihailov, Evelin
    Publication type:
    Article
    17

    Common variants associated with general and MMR vaccine-related febrile seizures.

    Published in:
    Nature Genetics, 2014, v. 46, n. 12, p. 1274, doi. 10.1038/ng.3129
    By:
    • Feenstra, Bjarke;
    • Pasternak, Björn;
    • Geller, Frank;
    • Carstensen, Lisbeth;
    • Svanström, Henrik;
    • Hviid, Anders;
    • Wang, Tongfei;
    • Huang, Fen;
    • Jan, Lily Yeh;
    • Eitson, Jennifer L;
    • Schoggins, John W;
    • Hollegaard, Mads V;
    • Hougaard, David M;
    • Vestergaard, Mogens;
    • Melbye, Mads
    Publication type:
    Article
    18

    Genome-wide association analyses identify variants in developmental genes associated with hypospadias.

    Published in:
    Nature Genetics, 2014, v. 46, n. 9, p. 957, doi. 10.1038/ng.3063
    By:
    • Geller, Frank;
    • Feenstra, Bjarke;
    • Carstensen, Lisbeth;
    • Pers, Tune H;
    • van Rooij, Iris A L M;
    • Körberg, Izabella Baranowska;
    • Choudhry, Shweta;
    • Karjalainen, Juha M;
    • Schnack, Tine H;
    • Hollegaard, Mads V;
    • Feitz, Wout F J;
    • Roeleveld, Nel;
    • Hougaard, David M;
    • Hirschhorn, Joel N;
    • Franke, Lude;
    • Baskin, Laurence S;
    • Nordenskjöld, Agneta;
    • van der Zanden, Loes F M;
    • Melbye, Mads
    Publication type:
    Article
    19

    New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.

    Published in:
    Nature Genetics, 2013, v. 45, n. 1, p. 76, doi. 10.1038/ng.2477
    By:
    • Horikoshi, Momoko;
    • Yaghootkar, Hanieh;
    • Mook-Kanamori, Dennis O;
    • Sovio, Ulla;
    • Taal, H Rob;
    • Hennig, Branwen J;
    • Bradfield, Jonathan P;
    • St Pourcain, Beate;
    • Evans, David M;
    • Charoen, Pimphen;
    • Kaakinen, Marika;
    • Cousminer, Diana L;
    • Lehtimäki, Terho;
    • Kreiner-Møller, Eskil;
    • Warrington, Nicole M;
    • Bustamante, Mariona;
    • Feenstra, Bjarke;
    • Berry, Diane J;
    • Thiering, Elisabeth;
    • Pfab, Thiemo
    Publication type:
    Article
    20
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    24

    Determination of NAT2 acetylation status in the Greenlandic population.

    Published in:
    Archives of Toxicology, 2016, v. 90, n. 4, p. 883, doi. 10.1007/s00204-015-1501-1
    By:
    • Geller, Frank;
    • Soborg, Bolette;
    • Koch, Anders;
    • Michelsen, Sascha;
    • Bjorn-Mortensen, Karen;
    • Carstensen, Lisbeth;
    • Birch, Emilie;
    • Nordholm, Anne;
    • Johansen, Marie;
    • Børresen, Malene;
    • Feenstra, Bjarke;
    • Melbye, Mads
    Publication type:
    Article
    25

    Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.

    Published in:
    Nature Communications, 2017, v. 8, n. 6, p. 15789, doi. 10.1038/ncomms15789
    By:
    • Sigurdsson, Snaevar;
    • Alexandersson, Kristjan F.;
    • Sulem, Patrick;
    • Feenstra, Bjarke;
    • Gudmundsdottir, Steinunn;
    • Halldorsson, Gisli H.;
    • Olafsson, Sigurgeir;
    • Sigurdsson, Asgeir;
    • Rafnar, Thorunn;
    • Thorgeirsson, Thorgeir;
    • Sørensen, Erik;
    • Nordholm-Carstensen, Andreas;
    • Burcharth, Jakob;
    • Andersen, Jens;
    • Jørgensen, Henrik Stig;
    • Possfelt-Møller, Emma;
    • Ullum, Henrik;
    • Thorleifsson, Gudmar;
    • Masson, Gisli;
    • Thorsteinsdottir, Unnur
    Publication type:
    Article
    26

    Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis.

    Published in:
    Nature Communications, 2016, v. 7, n. 7, p. 12350, doi. 10.1038/ncomms12350
    By:
    • Steinthorsdottir, Valgerdur;
    • Thorleifsson, Gudmar;
    • Aradottir, Kristrun;
    • Feenstra, Bjarke;
    • Sigurdsson, Asgeir;
    • Stefansdottir, Lilja;
    • Kristinsdottir, Anna M.;
    • Zink, Florian;
    • Halldorsson, Gisli H.;
    • Munk Nielsen, Nete;
    • Geller, Frank;
    • Melbye, Mads;
    • Gudbjartsson, Daniel F.;
    • Geirsson, Reynir T.;
    • Thorsteinsdottir, Unnur;
    • Stefansson, Kari
    Publication type:
    Article
    27

    Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight.

    Published in:
    2016
    By:
    • Tyrrell, Jessica;
    • Richmond, Rebecca C.;
    • Palmer, Tom M.;
    • Feenstra, Bjarke;
    • Rangarajan, Janani;
    • Metrustry, Sarah;
    • Cavadino, Alana;
    • Paternoster, Lavinia;
    • Armstrong, Loren L.;
    • G. De Silva, N. Maneka;
    • Wood, Andrew R.;
    • Horikoshi, Momoko;
    • Geller, Frank;
    • Myhre, Ronny;
    • Bradfield, Jonathan P.;
    • Kreiner-Møller, Eskil;
    • Huikari, Ville;
    • Painter, Jodie N.;
    • Hottenga, Jouke-Jan;
    • Allard, Catherine
    Publication type:
    journal article
    28

    STUDY OF CORRELATION BETWEEN THE NAT2 PHENOTYPE AND GENOTYPE STATUS AMONG GREENLANDIC INUIT.

    Published in:
    EXCLI Journal, 2018, v. 17, p. 1043, doi. 10.17179/excli2018-1671
    By:
    • Kristensen, Emilie Birch;
    • Yakimov, Victor;
    • Bjorn-Mortensen, Karen;
    • Soborg, Bolette;
    • Koch, Anders;
    • Andersson, Mikael;
    • Kristensen, Kasper Birch;
    • Michelsen, Sascha Wilk;
    • Skotte, Line;
    • Bjerregaard, Anne Ahrendt;
    • Blaszkewicz, Meinolf;
    • Golka, Klaus;
    • Hengstler, Jan G.;
    • Feenstra, Bjarke;
    • Melbye, Mads;
    • Geller, Frank
    Publication type:
    Article
    29

    Maternal Contributions to Preterm Delivery.

    Published in:
    American Journal of Epidemiology, 2009, v. 170, n. 11, p. 1358, doi. 10.1093/aje/kwp324
    By:
    • Boyd, Heather A.;
    • Poulsen, Gry;
    • Wohlfahrt, Jan;
    • Murray, Jeffrey C.;
    • Feenstra, Bjarke;
    • Melbye, Mads
    Publication type:
    Article
    30

    Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study.

    Published in:
    BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-77
    By:
    • Kim, Jinsil;
    • Stirling, Kara J.;
    • Cooper, Margaret E.;
    • Ascoli, Mario;
    • Momany, Allison M.;
    • McDonald, Erin L.;
    • Ryckman, Kelli K.;
    • Rhea, Lindsey;
    • Schaa, Kendra L.;
    • Cosentino, Viviana;
    • Gadow, Enrique;
    • Saleme, Cesar;
    • Shi, Min;
    • Hallman, Mikko;
    • Plunkett, Jevon;
    • Kari A.;
    • Muglia, Louis J.;
    • Feenstra, Bjarke;
    • Geller, Frank;
    • Boyd, Heather A.
    Publication type:
    Article
    31

    The derived allele of a novel intergenic variant at chromosome 11 associates with lower body mass index and a favorable metabolic phenotype in Greenlanders.

    Published in:
    PLoS Genetics, 2020, v. 16, n. 1, p. 1, doi. 10.1371/journal.pgen.1008544
    By:
    • Andersen, Mette K.;
    • Jørsboe, Emil;
    • Skotte, Line;
    • Hanghøj, Kristian;
    • Sandholt, Camilla H.;
    • Moltke, Ida;
    • Grarup, Niels;
    • Kern, Timo;
    • Mahendran, Yuvaraj;
    • Søborg, Bolette;
    • Bjerregaard, Peter;
    • Larsen, Christina V. L.;
    • Dahl-Petersen, Inger K.;
    • Tiwari, Hemant K.;
    • Feenstra, Bjarke;
    • Koch, Anders;
    • Wiener, Howard W.;
    • Hopkins, Scarlett E.;
    • Pedersen, Oluf;
    • Melbye, Mads
    Publication type:
    Article
    32
    33

    X-Chromosomal Maternal and Fetal SNPs and the Risk of Spontaneous Preterm Delivery in a Danish/Norwegian Genome-Wide Association Study.

    Published in:
    PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0061781
    By:
    • Myking, Solveig;
    • Boyd, Heather A.;
    • Myhre, Ronny;
    • Feenstra, Bjarke;
    • Jugessur, Astanand;
    • Devold Pay, Aase S.;
    • Østensen, Ingrid H. G.;
    • Morken, Nils-Halvdan;
    • Busch, Tamara;
    • Ryckman, Kelli K.;
    • Geller, Frank;
    • Magnus, Per;
    • Gjessing, Håkon K.;
    • Melbye, Mads;
    • Jacobsson, Bo;
    • Murray, Jeffrey C.
    Publication type:
    Article
    34
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    39

    Genetic regulation of spermine oxidase activity and cancer risk: a Mendelian randomization study.

    Published in:
    Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-97069-x
    By:
    • Fadista, João;
    • Yakimov, Victor;
    • Võsa, Urmo;
    • Hansen, Christine S.;
    • Kasela, Silva;
    • Skotte, Line;
    • Geller, Frank;
    • Courraud, Julie;
    • Esko, Tõnu;
    • Kukuškina, Viktorija;
    • Buil, Alfonso;
    • Melbye, Mads;
    • Werge, Thomas M.;
    • Hougaard, David M.;
    • Milani, Lili;
    • Bybjerg-Grauholm, Jonas;
    • Cohen, Arieh S.;
    • Feenstra, Bjarke
    Publication type:
    Article
    40

    Acute and persistent symptoms in non-hospitalized PCR-confirmed COVID-19 patients.

    Published in:
    Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-92045-x
    By:
    • Bliddal, Sofie;
    • Banasik, Karina;
    • Pedersen, Ole Birger;
    • Nissen, Janna;
    • Cantwell, Lisa;
    • Schwinn, Michael;
    • Tulstrup, Morten;
    • Westergaard, David;
    • Ullum, Henrik;
    • Brunak, Søren;
    • Tommerup, Niels;
    • Feenstra, Bjarke;
    • Geller, Frank;
    • Ostrowski, Sisse Rye;
    • Grønbæk, Kirsten;
    • Nielsen, Claus Henrik;
    • Nielsen, Susanne Dam;
    • Feldt-Rasmussen, Ulla
    Publication type:
    Article
    41
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    Genetic regulation of gene expression in the epileptic human hippocampus.

    Published in:
    Human Molecular Genetics, 2017, v. 26, n. 9, p. 1759, doi. 10.1093/hmg/ddx061
    By:
    • Mirza, Nasir;
    • Appleton, Richard;
    • Burn, Sasha;
    • du Plessis, Daniel;
    • Duncan, Roderick;
    • Farah, Jibril Osman;
    • Feenstra, Bjarke;
    • Hviid, Anders;
    • Josan, Vivek;
    • Mohanraj, Rajiv;
    • Shukralla, Arif;
    • Sills, Graeme J.;
    • Marson, Anthony G.;
    • Pirmohamed, Munir
    Publication type:
    Article
    46

    Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 2, p. 389, doi. 10.1093/hmg/ddv472
    By:
    • Felix, Janine F.;
    • Bradfield, Jonathan P.;
    • Monnereau, Claire;
    • van der Valk, Ralf J. P.;
    • Stergiakouli, Evie;
    • Chesi, Alessandra;
    • Gaillard, Romy;
    • Feenstra, Bjarke;
    • Thiering, Elisabeth;
    • Kreiner-Møller, Eskil;
    • Mahajan, Anubha;
    • Pitkänen, Niina;
    • Joro, Raimo;
    • Cavadino, Alana;
    • Huikari, Ville;
    • Franks, Steve;
    • Groen-Blokhuis, Maria M.;
    • Cousminer, Diana L.;
    • Marsh, Julie A.;
    • Lehtimäki, Terho
    Publication type:
    Article
    47

    Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 18, p. 3807, doi. 10.1093/hmg/ddt231
    By:
    • Fatemifar, Ghazaleh;
    • Hoggart, Clive J.;
    • Paternoster, Lavinia;
    • Kemp, John P.;
    • Prokopenko, Inga;
    • Horikoshi, Momoko;
    • Wright, Victoria J.;
    • Tobias, Jon H.;
    • Richmond, Stephen;
    • Zhurov, Alexei I.;
    • Toma, Arshed M.;
    • Pouta, Anneli;
    • Taanila, Anja;
    • Sipila, Kirsi;
    • Lähdesmäki, Raija;
    • Pillas, Demetris;
    • Geller, Frank;
    • Feenstra, Bjarke;
    • Melbye, Mads;
    • Nohr, Ellen A.
    Publication type:
    Article
    48

    Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5–CHRNA3–CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 24, p. 5344, doi. 10.1093/hmg/dds372
    By:
    • Tyrrell, Jessica;
    • Huikari, Ville;
    • Christie, Jennifer T.;
    • Cavadino, Alana;
    • Bakker, Rachel;
    • Brion, Marie-Jo A.;
    • Geller, Frank;
    • Paternoster, Lavinia;
    • Myhre, Ronny;
    • Potter, Catherine;
    • Johnson, Paul C.D.;
    • Ebrahim, Shah;
    • Feenstra, Bjarke;
    • Hartikainen, Anna-Liisa;
    • Hattersley, Andrew T.;
    • Hofman, Albert;
    • Kaakinen, Marika;
    • Lowe, Lynn P.;
    • Magnus, Per;
    • McConnachie, Alex
    Publication type:
    Article
    49

    Sequence variants at CYP1A1–CYP1A2 and AHR associate with coffee consumption.

    Published in:
    Human Molecular Genetics, 2011, v. 20, n. 10, p. 2071, doi. 10.1093/hmg/ddr086
    By:
    • Sulem, Patrick;
    • Gudbjartsson, Daniel F.;
    • Geller, Frank;
    • Prokopenko, Inga;
    • Feenstra, Bjarke;
    • Aben, Katja K.H.;
    • Franke, Barbara;
    • den Heijer, Martin;
    • Kovacs, Peter;
    • Stumvoll, Michael;
    • Mägi, Reedik;
    • Yanek, Lisa R.;
    • Becker, Lewis C.;
    • Boyd, Heather A.;
    • Stacey, Simon N.;
    • Walters, G. Bragi;
    • Jonasdottir, Adalbjorg;
    • Thorleifsson, Gudmar;
    • Holm, Hilma;
    • Gudjonsson, Sigurjon A.
    Publication type:
    Article