Publications

Journal articles

2023

Beaumont RN, Flatley C, Vaudel M, Wu X, Chen J, et al. Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Nature Genetics 2023; 55:1807–1819. PubMed doi

Pasanen A, Karjalainen MK, FinnGen, Zhang G, Tiensuu H, Haapalainen AM, Ojaniemi M, Feenstra B, Jacobsson B, Palotie A, Laivuori H, Muglia LJ, Rämet M, Hallman M. Meta-analysis of genome-wide associations studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci. PLoS Genetics 2023; 19(10), e1010982. PubMed doi

Budu-Aggrey A, Kilanowski A, Sobczyk MK, 23andMe Research Team, Shringarpure SS, et al. European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation. Nature Communications 2023; 14 (1), 6172. PubMed doi

The COVID-19 Host Genetics Initiative. A second update on mapping the human genetic architecture of COVID-19. Nature 2023; 621: E7–E26. PubMed doi

Solé-Navais P, Flatley C, Steinthorsdottir V, Vaudel M, Juodakis J, et al. Genetic effects on the timing of parturition and links to fetal birth weight. Nature Genetics 2023; 55:559-567. PubMed doi

2022

Yengo L, Vedantam S, Marouli E, Sidorenko J, Bartell E, et al. A Saturated Map of common Genetic Variants Associated with Human Height from 5.4 Million Indi-viduals of Diverse Ancestries. Nature 2022; 610:704-712. PubMed doi

Wang Z, Emmerich A, Pillon NJ, Moore T, Hemerich D, et al. Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Nature Genetics 2022; 59:1332-1344. PubMed doi

Fadista J, Skotte L, Karjalainen J, Abner E, Sørensen E, Ullum H, Werge T, iPSYCH Group, Esko T, Milani L, Palotie A, Daly M, FinnGen Consortium, Melbye M, Feenstra B, Geller F. Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci. Nature Communications 2022; 13:2300. PubMed doi

Vogelezang S, Bradfield JP, the Early Growth Genetics Consortium, Grant SFA, Felix JF, Jaddoe VWV. Genetics of early-life head circumference and genetic correlations with neurological, psychiatric and cognitive outcomes. BMC Medical Genomics 2022; 15:124. PubMed doi

Jørsboe E, Andersen MK, Skotte L, Færgeman NJ, Hanghøj K, Santander CG, Senftleber NK, Diaz LJ, Tvermosegaard M, Waples RK, Geller F, Bjerregaard P, Melbye M, Larsen CVL, Feenstra B, Koch A, Jørgensen ME, Grarup N, Moltke I, Albrechtsen A, Hansen T. An LDLR missense variant poses high risk of familial hypercholesterolemia in 30% of Greenlanders and offers potential for early cardiovascular disease intervention. Human Genetics and Genomics Advances 2022; 3:100118. PubMed doi

Skotte L, Fadista J, Bybjerg-Grauholm J, Appadurai V, Hildebrand MS, Hansen TF, Banasik K, Grove J, Albiñana C, Geller F, Bjurström CF, Vilhjálmsson BJ, Coleman M, Damiano JA, Burgess R, Scheffer IE, Pedersen OV, Erikstrup C, Westergaard D, Nielsen KR, Sørensen E, Bruun MT, Liu X, Hjalgrim H, Pers TH, Mortensen PB, Mors O, Nordentoft M, Dreier JW, Børglum AD, Christensen J, David M Hougaard DM, Buil A, Hviid A, Melbye M, Ullum H, Berkovic SF, Werge T, Feenstra B. Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes. Brain 2022; 145:555–568. PubMed doi

Christensen KJ, Dreier JW, Skotte L, Feenstra B, Grove J, Børglum AD, Mitrovic M, Cotsapas C, Christensen J. Seasonal variation and risk of febrile seizures; a Danish nationwide cohort study. Neuroepidemiology 2022; 56:138–145. PubMed doi

Andersen MK, Skotte L, Jørsboe E, Polito R, Stæger FF, Aldiss P, Hanghøj K, Waples RK, Santander CG, Grarup N, Dahl-Petersen IK, Diaz LJ, Overvad M, Senftleber NK, Søborg B, Larsen CVL, Lemoine C, Pedersen O, Feenstra B, Bjerregaard P, Melbye M, Jørgensen ME, Færgeman NJ, Koch A, Moritz T, Gillum MP, Moltke I, Hansen T, Albrechtsen A. Loss of sucrase-isomaltase function increases acetate levels and improves metabolic health in Greenlandic cohorts. Gastroenterology 2022; 162:1171-1182. PubMed doi

2021

Fadista J, Yakimov V, Võsa U, Hansen CS, Kasela S, Skotte L, Geller F, Courraud J,Esko T, Kukuškina V, Buil A, Melbye M, Werge TM, Hougaard DM, Milani L,Bybjerg‑Grauholm J, Cohen AS, Feenstra B. Genetic regulation of spermine oxidase activity and cancer risk: a Mendelian randomization study. Scientific Reports; 11: 17463. PubMed doi

Bliddal S, Banasik K, Pedersen OB, Nissen J, Cantwell L, Schwinn M, Tulstrup M,Westergaard D, Ullum H, Brunak S, Tommerup N, Feenstra B, Geller F, Ostrowski SR, Grønbæk K, Nielsen CH, Nielsen SD, Feldt-Rasmussen U. Acute and persistent symptoms in non-hospitalized PCR-confirmed COVID-19 patients. Scientific Reports; 11: 13153.PubMed doi

Christensen KJ, Dreier JW, Skotte L, Feenstra B, Grove J, Børglum A, Mitrovic M, Cotsapas C, Christensen J. Birth characteristics and risk of febrile seizures. Acta Neurologica Scandinavia; 144(1), 51-57. PubMed doi

Fadista J, Kraven LM, Karjalainen J, Andrews SJ, Geller F, The COVID-19 Host Genetics Initiative, Baillie JK, Wain LV, Jenkins RG, Feenstra B. Shared genetic etiology between idiopathic pulmonary fibrosis and COVID-19 severity. EBioMedicine2021; 65: 103277.
PubMed doi.

Fadista J, Skotte L, Courraud J, Geller F, Gørtz S, Wohlfahrt J, Melbye M, Cohen AS, Feenstra B. Integrating genetics with newborn metabolomics in infantile hypertrophic pyloric stenosis. Metabolomics 2021; 17:7. PubMeddoi

Cuellar-Partida G, Tung JY, Eriksson N, Albrecht E, Aliev F, Andreassen OA, Barroso I, Beckmann JS, Boks MP, Boomsma DI, Boyd HA, Breteler MMB, Campbell H, Chasman DI, Cherkas LF, Davies G, de Geus EJC, Deary IJ, Deloukas P, Dick DM, Duffy DL, Eriksson JG, Esko T, Feenstra B, Geller F, Gieger C, Giegling I, Gordon SD, Han J, Hansen TF, Hartmann AM, Hayward C, Heikkilä K, Hicks AA, Hirschhorn JN, Hottenga J-J, Huffman JE, Hwang L-D, Ikram MA, Kaprio J, Kemp JP,Khaw K-T, Klopp N, Konte B, Kutalik Z, Lahti J, Li X, Loos RJF, Luciano M, Magnusson SH, Mangino M, Marques-Vidal P, Martin NG, McArdle WL, McCarthy MI, Medina-Gomez C, Melbye M, Melville SA, Metspalu A, Milani L, Mooser V, Nelis M, Nyholt DR, O’Connell KS, Ophoff RA, Palmer C, Palotie A, Palviainen T, Pare G, Paternoster L, Peltonen L, Penninx BWJH, Polasek O, Pramstaller PP, Prokopenko I, Raikkonen K, Ripatti S, Rivadeneira F, Rudan I, Rujescu D, Smit JH, Smith GD, Smoller JW, Soranzo N, Spector TD, St Pourcain B, Starr JM, Stefánsson H, Steinberg S, Teder-Laving M, Thorleifsson G, Stefansson K, Timpson NJ, Uitterlinden AG, van Duijn CM, van Rooij FJA, Vink JM, Vollenweider P, Vuoksimaa E, Waeber G, Wareham NJ, Warrington N, Waterworth D, Werge T, Wichmann H-E, Widen E, Willemsen G, Wright AF, Wright MJ, Xu M, Zhao JH, Kraft P, Hinds DA, Lindgren CM, Magi R, Neale BM, Evans DM, Medland SE. Genome-wide association study identifies 48 common genetic variants associated with handedness. Nature Human Behaviour 2021; 5, 59-70. PubMeddoi

2020

Krebs K, Bovijn J, Zheng N, Lepamets M, Censin JC, Jürgenson T, Särg D, Abner E,Laisk T, Luo Y, Skotte L, Geller F, Feenstra B, Wang W, Auton A, 23andMe Research Team, Raychaudhuri S, Esko T, Metspalu A, Laur S, Roden DM, Wei W-Q, Holmes MV, Lindgren CM, Phillips EJ, Mägi R, Milani L, Fadista J. **Genome-wide study identifies association between HLA-B*55:01 and self-reported penicillin allergy.** American Journal of Human Genetics 2020; 107(4), 612-621 PubMeddoi

Steinthorsdottir V, McGinnis R, Williams NO, Stefansdottir L, Thorleifsson G, Shooter S, Fadista J, Sigurdsson JK, Auro KM, Berezina G, Borges M-C, BumpsteadS, Bybjerg-Grauholm J, Colgiu I, Dolby VA, Dudbridge F, Engel SM, Franklin CS, Frigge ML, Frisbaek Y, Geirsson RT, Geller F, Gretarsdottir S, Gudbjartsson DF,Harmon Q, Hougaard DM, Hegay T, Helgadottir A, Hjartardottir S, Jääskeläinen T,Johannsdottir H, Jonsdottir I, Juliusdottir T, Kalsheker N, Kasimov A, Kemp JP, Kivinen K, Klungsøyr K, Lee WK, Melbye M, Miedzybrodska Z, Moffett A, Najmutdinova D, Nishanova F, Olafsdottir T, Perola M, Pipkin FB, Poston L, Prescott G, Saevarsdottir S, Salimbayeva D, Scaife PJ, Skotte L, Staines-Urias E, StefanssonOA, Sørensen KM, Thomsen LCV, Tragante V, Trogstad L, Simpson NAB, The FINNPEC Consortium, The GOPEC Consortium, Aripova T, Casas JP, Dominiczak AF, Walker JJ, Thorsteinsdottir U, Iversen A-C, Feenstra B, Lawlor DA, Boyd HA, Magnus P, Laivuori H, Zakhidova N, Svyatova G, Stefansson K, Morgan L. Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women. Nature Communications 2020; 11:5976. PubMeddoi.

Chen J, Bacelis J, Navais PS, Srivastava A, Juodakis J, Rouse A, Hallman M, Teramo K, Melbye M, Feenstra B, Freathy RM, Smith GD, Lawlor DA, Murray JC, Williams SM, Jacobsson B, Muglia LJ, Zhang G. 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. PLoS Medicine 2020; 17(8):e1003305. PubMeddoi

Liang L, Rasmussen M-LH, Piening B, Shen X, Chen S, Röst H, Snyder JK, Tibshirani R, Skotte L, Lee NCY, Contrepois K, Feenstra B, Zackriah H, Snyder M, Melbye M. Metabolic dynamics and prediction of gestational age and time to delivery in pregnant women. Cell 2020; 181, 1680-1692. PubMeddoi

Vogelezang S, Bradfield JP, Ahluwalia TS, Curtin JA, Lakka TA, et al. Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits. PLoS Genetics 2020; 16(10):e1008718. PubMed doi

Andersen MK, Jørsboe E, Skotte L, Hanghøj K, Sandholt CH, Moltke I, Grarup N, Kern T, Mahendran Y, Søborg B, Bjerregaard P, Larsen CVL, Dahl-Petersen IK, Tiwari HK, Feenstra B, Koch A, Wiener HW, Hopkins SE, Pedersen O, Melbye M, Boyer BB, Jørgensen ME, Albrechtsen A, Hansen T. The derived allele of a novel intergenic variant at chromosome 11 associates with lower body mass index and a favorable metabolic phenotype in Greenlanders. PLoS Genetics 2020; 16(1): e1008544.PubMed doi

2019

lark D, Okada Y, Moore K, Mason D, Pirastu N, et al. Associations of autozygosity with a broad range of human phenotypes. Nature Communications 2019; 10:4957. PubMed doi.

Liu Xs, Helenius Ds, Skotte Ls, Beaumont RN, Wielscher M, Geller F, Juodakis J, Mahajan A, Bradfield JP, Lin FTJ, Vogelezang S, Bustamante M, Ahluwalia TS, Pitkänen N, Wang CA, Bacelis J, Borges MC, Zhang G, Bedell BA, Rossi RM, Skogstrand K, Peng S, Thompson WK, Appadurai V, Lawlor DA, Kalliala I, Power C, McCarthy MI, Boyd HA, Marazita ML, Hakonarson H, Hayes MG, Scholtens DM, Rivadeneira F, Jaddoe VWV, Vinding RK, Bisgaard H, Knight BA, Pahkala K, Raitakari O, Helgeland Ø, Johansson S, Njølstad PR, Fadista J, Schork AJ, Nudel R, Miller DE, Chen X, Weirauch MT, Mortensen PB, Børglum AD, Nordentoft M, Mors O, Hao K, Ryckman KK, Hougaard DM, Kottyan LC, Pennell CE, Lyytikainen LP, Bønnelykke K, Vrijheid M, Felix JF, Lowe WL, Grant SFA, Hyppönen E, Jacobsson B, Jarvelin M-R, Muglia LJ, Murray JC, Freathy RM, Werge TM, Melbye M, Buil A, Feenstra B. Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration. Nature Communications2019; 10:3927. PubMed doi.

Alves AC, De Silva NMG, Karhunen V, Sovio U, Das S, et al. GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child and adult BMI. Science Advances 2019; 5(9), eaaw3095. PubMed doi.

Feenstra B, Gørtz S, Lund M, Ranthe MF, Geller F, Melbye M. Co-occurrence of infantile hypertrophic pyloric stenosis and congenital heart defects: a nationwide cohort study. Pediatric Research 2019; 85, 955-960. PubMed doi

Warrington NM, Beaumont RN, Horikoshi M, Day FR, Helgeland Ø, Laurin C, Bacelis J, Peng S, Hao K, Feenstra B, Wood AR, Mahajan A, Tyrrell J, Robertson NR, William Rayner N, Qiao Z, Moen G-HØ, Vaudel M, Marsit CJ, Chen J, Nodzenski M, Schnurr TM, Zafarmand MH, Bradfield JP, Grarup N, Kooijman MN, Li-Gao R, Geller F, Ahluwalia TS, Paternoster L, Rueedi R, Huikari V, Hottenga J-J, Lyytikäinen L-P, Cavadino A, Metrustry S, Cousminer DL, Wu Y, Thiering E, Wang CA, Have CT, Vilor-Tejedor N, Joshi PK, Painter JN, Ntalla I, Myhre R, Pitkänen N, van Leeuwen EM, Joro R, Lagou V, Richmond RC, Espinosa A, Barton SJ, Inskip HM, Holloway JW, Santa-Marina L, Estivill X, Ang W, Marsh JA, Reichetzeder C, Marullo L, Hocher B, Lunetta KL, Murabito JM, Relton CL, Kogevinas M, Chatzi L, Allard C, Bouchard L, Hivert M-F, Zhang G, Muglia LJ, Heikkinen J, Early Growth Genetics (EGG) Consortium, Morgen CS, van Kampen AHC, van Schaik BDC, Mentch FD, Langenberg C, Luan J, Scott RA, Zhao JH, Hemani G, Ring SM, Bennett AJ, Gaulton KJ, Fernandez-Tajes J, van Zuydam NR, Medina-Gomez C, de Haan HG, Rosendaal FR, Kutalik Z, Marques-Vidal P, Das S, Willemsen G, Mbarek H, Müller-Nurasyid M, Standl M, R Appel EV, Fonvig CE, Trier C, van Beijsterveldt CEM, Murcia M, Bustamante M, Bonas-Guarch S, Hougaard DM, Mercader JM, Linneberg A, Schraut KE, Lind PA, Medland SE, Shields BM, Knight BA, Chai J-F, Panoutsopoulou K, Bartels M, Sánchez F, Stokholm J, Torrents D, Vinding RK, Willems SM, Atalay M, Chawes BL, Kovacs P, Prokopenko I, Tuke MA, Yaghootkar H, Ruth KS, Jones SE, Loh P-R, Murray A, Weedon MN, Tönjes A, Stumvoll M, Michaelsen KF, Eloranta A-M, Lakka TA, van Duijn CM, Kiess W, Körner A, Niinikoski H, Pahkala K, Raitakari OT, Jacobsson B, Zeggini E, Dedoussis GV, Teo Y-Y, Saw S-M, Montgomery GW, Campbell H, Wilson JF, Vrijkotte TGM, Vrijheid M, de Geus EJCN, Hayes MG, Kadarmideen HN, Holm J-C, Beilin LJ, Pennell CE, Heinrich J, Adair LS, Borja JB, Mohlke KL, Eriksson JG, Widén EE, Hattersley AT, Spector TD, Kähönen M, Viikari JS, Lehtimäki T, Boomsma DI, Sebert S, Vollenweider P, Sørensen TIA, Bisgaard H, Bønnelykke K, Murray JC, Melbye M, Nohr EA, MookKanamori DO, Rivadeneira F, Hofman A, Felix JF, Jaddoe VWV, Hansen T, Pisinger C, Vaag AA, Pedersen O, Uitterlinden AG, Järvelin M-R, Power C, Hyppönen E, Scholtens DM, Lowe Jr WL, Davey Smith G, Timpson NJ, Morris AP, Wareham NJ, Hakonarson H, Grant SFA, Frayling TM, Lawlor DA, Njølstad PR, Johansson S, Ong KK, McCarthy MI, Perry JRB, Evans DM, Freathy RM. Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. Nature Genetics 2019; 51, 804-814. PubMed doi

Middeldorp CM, et al. The Early Growth Genetics (EGG) and Early Genetics and Lifecourse Epidemiology (EAGLE) Consortia: design, results and future prospects. European Journal of Epidemiology 2019; 34, 279-300. PubMeddoi

Bager P, Gørtz S, Feenstra B, Andersen NN, Jess T, Frisch M, Melbye M. Increased risk of inflammatory bowel disease in families with tonsillectomy: A Danish national cohort study. Epidemiology 2019; 30, 256–262. PubMeddoi.

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, Mills JL, Melbye M, Feenstra B. Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis. Human Molecular Genetics 2019; 28, 332–340. PubMeddoi.

2018

Kristensen EB, Yakimov V, Bjørn-Mortensen K, Søborg B, Koch A, Andersson M, Kristensen KB, Michelsen SW, Skotte L, Bjerregaard AA, Blaszkewicz M, Golka K, Hengstler JG, Feenstra B, Melbye M, Geller F. Study of correlation between the NAT2 phenotype and genotype status among Greenlandic Inuit. EXCLI journal 2018; 17, 1043-1053 PubMeddoi

Ligthart S, Vaez A, Võsa U, Stathopoulou MG, de Vries PS, et al. Genome-wide association analyses of >200,000 individuals identify 58 genetic loci for chronic in-flammation and highlights pathways that link inflammation and complex disorders. American Journal of Human Genetics 2018; 103, 691-706. PubMeddoi.

Beaumont RN, Warrington NM, Cavadino A, Tyrrell J, Nodzenski M, Horikoshi M, Geller F, Myhre R, Richmond RC, Paternoster L, Bradfield JP, Kreiner-Møller E,Huikari V, Metrustry S, Lunetta KL, Painter JN, Hottenga J-J, Allard C, Barton SJ,Espinosa A, Marsh JA, Potter C, Zhang G, Ang W, Berry DJ, Bouchard L, Das S, Early Growth Genetics (EGG) Consortium, Hakonarson H, Heikkinen J, Helgeland Ø,Hocher B, Hofman A, Inskip HM, Jones SE, Kogevinas M, Lind PA, Marullo L, Medland SE, Murray A, Murray JC, Njølstad PR, Nohr EA, Reichetzeder C, Ring SM,Ruth KS, Santa-Marina L, Scholtens DM, Sebert S, Sengpiel V, Tuke MA, Vaudel M, Weedon MN, Willemsen G, Wood AR, Yaghootkar H, Muglia LJ, Bartels M, Relton CL, Pennell CE, Chatzi L, Estivill X, Holloway JW, Boomsma DI, Montgomery GW, Murabito JM, Spector TD, Power C, Järvelin M-R, Bisgaard H, SFA Grant, Sørensen TIA, Jaddoe VW, Jacobsson B, Melbye M, McCarthy MI, Hattersley AT, Hayes MG, Frayling TM, Hivert M-F, Felix JF, Hyppönen E, Lowe, Jr. WL, Evans DM, Lawlor DA, Feenstra B, Freathy RM. Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics. Human Molecular Genetics 2018; 27, 742-756.PubMeddoi

Fadista J, Lund M, Skotte L, Geller F, Nandakumar P, Chatterjee S, Matsson H, Löf-Granström A, Wester T, Salo P, Virtanen V, Carstensen L, Bybjerg-Grauholm J, Hougaard D, Pakarinen M, Perola M, Nordenskjöld A, Chakravarti A, Melbye M, Feenstra B. Genome-wide association study of Hirschsprung disease detects a novel low frequency variant at the RET locus. European Journal of Human Genetics 2018; 26, 561–56 PubMeddoi.

Bager P, Corn G, Wohlfahrt J, Boyd HA, Feenstra B, Melbye M. Familial aggregation of tonsillectomy in early childhood and adolescence. Clinical Epidemiology 2018; 10, 97–105. PubMeddoi

Haworth S, Shungin D, van der Tas JT, Vucic S, Medina-Gomez, C, Yakimov V,Feenstra B, et al. Consortium genome-wide meta-analysis for childhood dental caries traits. Human Molecular Genetics 2018; 17, 3113-3127.PubMeddoi.

Jonsson L, Magnusson TE, Thordarson A, Jonsson T, Geller F, Feenstra B, Melbye M, Nohr EA, Vucic S, Dhamo B, Rivadeneira F, Ongkosuwito EM, Wolvius EB, Leslie EJ, Marazita ML, Howe BJ, Uribe LM, Alonso I, Santos M, Pinho T, Jonsson R, Audolfsson G, Nawaz MS, Olafsson S, Gustafsson O, Ingason A, Unnsteinsdottir U, Bjornsdottir G, Walters GB, Zervas M, Oddsson A, Gudbjartsson DF, Steinberg S, Stefansson H, Stefansson K. Rare and common variants conferring risk of Tooth Agenesis. Journal of Dental Research 2018; 97, 515-522 PubMeddoi

Demenais F, Margaritte-Jeannin P, Barnes KC, Cookson WOC, Altmüller J, et al. Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. Nature Genetics 2018; 50, 42-53. PubMeddoi

Alonso N, Estrada K, Albagha OME, Herrera L, Reppe S, et al. Identification of a novel locus on chromosome 2q13 which predisposes to clinical vertebral fractures independently of bone density. Annals of the Rheumatic Diseases 2018; 77, 378–385. PubMeddoi

Warrington NM, Richmond R, Feenstra B, Myhre R, Gaillard R, et al. Maternal and fetal genetic contribution to gestational weight gain. International Journal of Obesity 2018; 42, 775–784. PubMeddoi

2017

Zhang G, Feenstra B, Bacelis J, Liu X, Muglia LM, Juodakis J, Miller DE, Litterman N, Jiang P-P, Russell L, Hinds DA, Hu Y, 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. Genetic Associations with Gestational Duration and Spontaneous Preterm Birth. New England Journal of Medicine 2017; 377, 1156-1167. PubMeddoi

Macé A, Tuke MA, Deelen P, Kristiansson K, Mattsson H, Nõukas M, Sapkota Y, Schick U, Porcu E, Rüeger S, McDaid AF, Porteous D, Winkler TW, Salvi E, Shrine N, Liu X, Ang WQ, Zhang W, Feitosa MF, Venturini C, Van der Most PJ, Rosengren A, Wood AR, Beaumont RN, Jones SE, Ruth KS, Yaghootkar H, Tyrrell J, Havulinna AS, Boers H, Mägi R, Kriebel J, Müller-Nurasyid M, Perola M, Nieminen M, Lokki M-L, Kähönen M, Viikari JS, Geller F, Lahti J, Palotie A, Koponen P, Lundqvist A, Rissanen H, Bottinger EP, Afaq S, Wojczynski MK, Lenzini P, Nolte IM, Sparsø T,Schupf N, Christensen K, Perls TT, Newman AB, Werge T, Snieder H, Spector TD, Chambers JC, Koskinen S, Melbye M, Raitakari OT, Lehtimäki T, Tobin MD, Wain LV, Sinisalo J, Peters A, Meitinger T, Martin NG, Wray NR, Montgomery GW, Medland SE, Swertz MA, Vartiainen E, Borodulin K, Männistö S, Murray A, Bochud M, Jacquemont S, Rivadeneira F, Hansen TF, Oldehinkel AJ, Mangino M, Province MA, Deloukas P, Kooner JS, Freathy RM, Pennell C, Feenstra B, Strachan DP, Lettre G, Hirschhorn J, Cusi D, Heid IM, Hayward C, Männik K, Beckmann JS, Loos RJF, Nyholt DR, Metspalu A, Eriksson JG, Weedon MN, Salomaa V, Franke L, Reymond A, Frayling TM, Kutalik Z. CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits. Nature Communications 2017; 8:744. PubMeddoi

Sigurdsson S, Alexandersson KF, Sulem P, Feenstra B, Gudmundsdottir S, Halldorsson GH, Olafsson S, Sigurdsson A, Rafnar T, Thorgeirsson T, Sørensen E,Nordholm-Carstensen A, Burcharth J, Andersen J, Jørgensen HS, Possfelt-Møller E, Ullum H, Thorleifsson G, Masson G, Thorsteinsdottir U, Melbye M, Gudbjartsson DF, Stefansson T, Jonsdottir I, Stefansson K. Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis. Nature Communications 2017; 8:15789 PubMeddoi

Skotte L, Koch A, Yakimov V, Zhou S, Søborg B, Andersson M, Michelsen SW, Navne JE, Mistry JM, Dion PA, Petersen ML, Børresen ML, Rouleau GA, Geller F, Melbye M, Feenstra B. A CPT1A missense mutation associated with fatty acid metabolism and reduced height in Greenlanders. Circulation Cardiovascular Genetics 2017; 10 (3):e001618. PubMeddoi

Mirza N, Appleton R, Burn S, du Plessis D, Duncan R, Farah JO, Feenstra B, Hviid A, Josan V, Mohanraj R, Shukralla A, Sills GJ, Marson AG, Pirmohamed M. Genetic Regulation of Gene Expression in the Epileptic Human Hippocampus. Human Molecular Genetics 2017; 26, 1759-1769.PubMeddoi

Feenstra B, Bager P, Liu X, Hjalgrim H, Nohr EA, Hougaard DM, Geller F, Melbye M. Genome-wide association study identifies variants in HORMAD2 associated with tonsillectomy. Journal of Medical Genetics 2017; 54, 358-364. PubMeddoi

2016

Horikoshi M, Beaumont RN, Day FR, Warrington NM, Kooijman MN, Fernandez Tajes J, Feenstra B, and many others. Genome-wide associations for birth weight and correlations with adult disease. Nature 2016; 538, 248–252. PubMeddoi

Steinthorsdottir V, Thorleifsson G, Aradottir K, Feenstra B, Sigurdsson A, Stefansdottir L, Kristinsdottir AM, Zink F, Halldorsson GH, Nielsen NM, Geller F, Melbye M, Gudbjartsson DF, Geirsson RT, Thorsteinsdottir U, Stefansson K. Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis. Nature Communications 2016; 7:12350 PubMeddoi.

Tyrrell J, Richmond RC, Palmer TM, Feenstra B, Rangarajan J, et al. Genetic evidence for causal relationships between maternal obesity-related traits and birth weight. JAMA 2016; 315 (11): 1129-1140. PubMeddoi.

Felix JF, et al.Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index. Human Molecular Genetics 2016; 25 (2): 389-403. PubMeddoi.

Geller F, Søborg B, Koch A, Michelsen SW, Bjørn-Mortensen K, Carstensen L, Nordholm AC, Johansen MMB, Børresen ML, Feenstra B, Melbye M. Determination of NAT2 acetylation status in the Greenlandic population. Archives of Toxicology 2016; 90(4): 883-889. PubMeddoi

Ruth KS, Campbell PJ, Chew S, Lim EM, Hadlow N, Stuckey BGA, Brown SJ, Feenstra B, Joseph J, Surdulescu GL, Zheng HF, Richards JB, Murray A, Spector TD, Wilson SG, Perry JRB. Genome-wide association study with 1000 genomes imputation identifies signals for nine sex-hormone-related phenotypes. European Journal of Human Genetics 2016; 24: 284-290. PubMeddoi

2015

Winkler TW, et al. The influence of age and sex on genetic associations with adult body size and shape: a large-scale genome-wide interaction study. PLoS Genetics 2015; 11(10): e1005378. PubMeddoi

Paternoster L, et al. Multi-ethnic genome-wide association study of 21,000 cases and 95,000 controls identifies 10 new risk loci for atopic dermatitis. Nature Genetics 2015; 47: 1449-1456. PubMeddoi

Joshi PK et al. Directional dominance on stature and cognition in diverse human populations. Nature 2015; 523: 459-462. PubMeddoi

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, 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, BraggGresham JL, Buyske S, Demirkan A, Deng G, Ehret GB, Feenstra B, and many others. Genetic studies of body mass index yield new insights for obesity biology. Nature 2015; 518: 197-206. PubMeddoi

Machiela MJ et al. Characterization of large structural genetic mosaicism in human autosomes. American Journal of Human Genetics 2015, 96: 487-497. PubMeddoi

Cornelis MC, et al. Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption. Molecular Psychiatry 2015, 20: 647-656. PubMeddoi

van der Valk, RJP et al. A novel common variant in DCST2 is associated with length in early life and height in adulthood. Human Molecular Genetics 2015; 24: 1155-1168. PubMeddoi

2014

Feenstra B, Pasternak B, Geller F, Carstensen L, Wang T, Huang F, Eitson JL, Hollegaard MV, Svanström H, Vestergaard M, Hougaard DM, Schoggins JW, Jan LY, Melbye M, Hviid A.Common variants associated with general and MMR vaccinerelated febrile seizures. Nature Genetics 2014; 46: 1274-1282. PubMeddoi.

Wood AR, Esko T, Yang J, Vedantam S, Pers TH, Gustafsson S, Chu AY, Estrada K, Luan J, Kutálik Z, Amin N, Buchkovich ML, Croteau-Chonka DC, Day FR, Duan Y, Fall T, Fehrmann R, Ferreira T, Jackson AU, Karjalainen J, Lo KS, Locke AE, Mägi R,Mihailov E, Porcu E, Randall JC, Scherag A, Vinkhuyzen AAE, Westra H-J, Winkler TW, Workalemahu T, Zhao JH, Absher D, Albrecht E, Anderson D, Baron J, Beekman M, Demirkan A, Ehret GB, Feenstra B, and many others. Defining the role of common variation in the genomic and biological architecture of adult human height. Nature Genetics 2014; 46: 1173-1185. PubMeddoi

Geller F, Feenstra B, Carstensen L, Pers TH, van Rooij IALM, Baranowska KörbergI, Choudhry S, Karjalainen J, Schnack TH, Hollegaard MV, Feitz WFJ, Roeleveld N, Hougaard DM, Hirschhorn JN, Franke L, Baskin LS, Nordenskjöld A, van der Zanden LFM, Melbye M. Genome-wide association analyses identify variants in developmental genes associated with hypospadias. Nature Genetics 2014; 46: 957-963. PubMed doi

Perry JRB, Day F, Elks CE, Sulem P, Thompson DJ, Ferreira T, He C, Chasman DI, Esko T, Thorleifsson G, Albrecht E, Ang WQ, Corre T, Cousminer DL, Feenstra B, and 187 others. Parent-of-origin specific allelic associations among 106 genomic loci for age at menarche. Nature 2014; 514: 92-97 PubMeddoi

Lund M, Diaz L, Gørtz S, Feenstra B, Dunoe M, Juncker I, Eiberg H, Vissing J, Wohlfahrt J, Melbye M. Risk of Cancer in Relatives of Patients With Myotonic Dystrophy: a Population Based Cohort Study. European Journal of Neurology 2014; 21: 1192-1197. PubMeddoi.

Lund M, Pasternak B, Davidsen RB, Feenstra B, Krogh C, Diaz LJ, Wohlfahrt J, Melbye M. Use of Macrolides in Mother and Child and Risk of Infantile Hypertrophic Pyloric Stenosis: Nationwide Cohort Study. British Medical Journal 2014; 348:g1908. PubMeddoi

2013

Feenstra B, Geller F, Carstensen L, Romitti PA, Baranowska Körberg I, Bedell B, Krogh C, Fan R, Svenningsson A, Caggana M, Nordenskjöld A, Mills JL, Murray JC, Melbye M. Plasma Lipids, Genetic Variants near APOA1, and the Risk of Infantile Hypertrophic Pyloric Stenosis. JAMA 2013; 710 (7): 714-721. PubMeddoi

Zheng X, Feingold E, Ryckman KK, Shaffer JR, Boyd HA, Feenstra B, Melbye M, Marazita ML, Murray JC, Cuenco KT. Association of maternal CNVs in GSTT1/GSTT2 with smoking, preterm delivery, and low birth weight. Frontiers in Genetics 2013; volume 4: article 196. PubMeddoi

Kim J, Stirling KJ, Cooper ME, Ascoli M, Momany AM, McDonald EL, Ryckman KK,Rhea L, Schaa KL, Cosentino V, Gadow E, Saleme C, Shi M, Hallman M, Plunkett J,Teramo KA, Muglia LJ, Feenstra B, Geller F, Boyd HA, Melbye M, Marazita ML,Dagle JM, Murray JC. Sequence variants in oxytocin pathway genes and pretermbirth: a candidate gene association study. BMC Medical Genetics 2013; 14(1), 77. PubMeddoi

Fatemifar G, Hoggart C, Paternoster L, Kemp JP, Prokopenko I, Horikoshi M, Wright VJ, Tobias JH, Richmond S, Zhurov AI, Toma AM, Pouta A, Taanila A, Sipila K, Lähdesmäki R, Pillas D, Geller F, Feenstra B, Melbye M, Nohr EA, Ring SM, St Pourcain B, Timpson NJ, Smith GD, Jarvelin M-R, Evans DM. Genome-Wide Association Study of Primary Tooth Eruption Identifies Pleiotropic Loci Associated With Height and Craniofacial Distances. Human Molecular Genetics 2013; 22(18): 3807-3817 PubMeddoi

Myking S, Boyd H, Myhre R, Feenstra B, Jugessur A, Devold Pay AS, Østensen IHG, Morken N-H, Busch T, Ryckman KK, Geller F, Magnus P, Gjessing HK, Melbye M, Jacobsson B, Murray JC. X-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association study. PLoS One 2013; 8 (4), e61781. PubMeddoi

Fernández-Rhodes L, Demerath EW, Cousminer DL, Tao R, Dreyfus JG, Esko T, Smith AV, Harris TB, McArdle PF, Yerges-Armstrong LM, Elks CE, Strachan DP, Kutalik Z, Vollenweider P, Feenstra B, and 52 others. Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. Am. J. Epidemiol. 2013; 178 (3): 451-460. PubMeddoi

Horikoshi M, Yaghootkar H, Mook-Kanamori DO, Sovio U, Taal HR, Hennig BJ, Bradfield JP, St. Pourcain B, Evans DM, Charoen P, Kaakinen M, Cousminer DL, Lehtimäki T, Kreiner-Møller E, Warrington NM, Bustamante M, Feenstra B, and 133 others. Novel loci associated with birth weight reveal genetic links between intrauterine growth and adult height and metabolism. Nature Genetics 2013; 45: 76-82. PubMeddoi

2012

Tyrrell J, Huikari V, Christie JT, Cavadino A, Bakker R, Brion M-J A, Geller F, Paternoster L, Myhre R, Potter C, Johnson PCD, Ebrahim S, Feenstra B, and 31 others.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. Human Molecular Genetics 2012; 21: 5344-58. PubMed doi.

Alleman B, Myking S, Ryckman KK, Myhre R, Feingold E, Feenstra B, Geller F, Boyd HA, Shaffer JR, Zhang Q, Begum F, Crosslin D, Doheny KF, Pugh EW, Pay A, Østensen I, Morken N-H, Magnus P, Marazita ML, Jacobsson B, Melbye M, Murray JC. No Observed Association for Mitochondrial SNPs with Preterm Delivery and related outcomes. Pediatric Research 2012; 72: 539-544. PMCID: PMC3694399.PubMeddoi

Laurie CC, Laurie CA, Rice K, Doheny KF, Zelnick LR, McHugh CP, Ling H, Hetrick KN, Pugh EW, Amos C, Wei Q, Wang L, Lee JE, Barnes KC, Hansel NN, Mathias R, Daley D, Beaty TH, Scott AF, Ruczinski I, Scharpf RB, Bierut LJ, Hartz SM, Landi MT, Freedman ND, Goldin LR, Ginsburg D, Li J, Desch KC, Strom SS, Blot WJ, Signorello LB, Ingles SA, Chanock SJ, Berndt SI, Le Marchand L, Henderson BE, Monroe KR, Heit JA, de Andrade M, Armasu SM, Regnier C, Lowe WL, Hayes MG, Marazita ML, Feingold E, Murray JC, Melbye M, Feenstra B, and 24 others. Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nature Genetics 2012; 44: 642-650. PubMeddoi.

Ekstrøm CT, Feenstra B. Detecting Sample Misidentifications in Genetic Association Studies. Statistical Applications in Genetics and Molecular Biology 2012; 11 (3): article 13. PubMeddoi

Taal HR, St Pourcain B, Thiering E, Das S, Mook- Kanamori DO, Warrington NM, Kaakinen M, Kreiner-Møller E, Bradfield JP, Freathy RM, Geller F, Guxens M, Cousminer DL, Kerkhof M, Timpson NJ, Ikram MA, Beilin LJ, Bønnelykke K, Buxton JL, Charoen P, Chawes BLK, Eriksson J, Evans DM, Hofman A, Kemp JP, Kim CE, Klopp N, Lahti J, Lye SJ, McMahon G, Mentch FD, Müller M, O’Reilly PF, Prokopenko I, Rivadeneira F, Steegers EAP, Sunyer J, Tiesler C, Yaghootkar H, the Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium, Breteler MMB, Debette S, Fornage M, Gudnason V, Launer LJ, van der Lugt A, Mosley TH, Seshadri S, Smith AV, Vernooij MW, the Early Genetics & Lifecourse Epidemiology (EAGLE) consortium, Blakemore AIF, Chiavacci RM, Feenstra B, and 34 others. Common genetic variants in SBNO1, and near HMGA2 and CRHR1/MAPT affect infant head circumference. Nature Genetics 2012; 44: 532-538.

Zheng X, Shaffer JR, McHugh CP, Laurie CC, Feenstra B, Melbye M, Murray JC, Marazita ML, Feingold E. Using Family Data as a Verification Standard to Evaluate Copy Number Variation Calling Strategies for Genetic Association Studies. Genetic Epidemiology; 36: 253-262 PubMeddoi.

Feenstra B, Geller F, Krogh C, Hollegaard MV, Gørtz S, Boyd HA, Murray JC, Hougaard DM, Melbye M. Common Variants near MBNL1 and NKX2-5 are Associated with Infantile Hypertrophic Pyloric Stenosis. Nature Genetics 2012; 44: 334-337. PubMeddoi.

Fode P, Larsen AR, Feenstra B, Jespersgaard C, Fowler VG Jr, Skov RL, The Danish SAB Study Group Consortium, Stegger M, Andersen PS. Genetic variability in beta-defensins is not associated with susceptibility to staphylococcus aureus bacteremia. PLoS One 2012; 7: e32315. PubMeddoi

Paternoster L, Standl M, Chen C-M, Ramasamy A, Bønnelykke K, Duijts L, Ferreira MA, Alves AC, Thyssen JP, Albrecht E, Baurecht H, Feenstra B, and 98 others. Meta-analysis of genome-wide association studies on atopic dermatitis identifies three novel risk loci. Nature Genetics 2012; 44: 187-192. PubMed doi

Urayama KY, Jarrett RF, Hjalgrim H, Diepstra A, Kamatani Y, Chabrier A, Gaborieau V, Boland A , Nieters A, Becker N, Foretova L, Benavente Y, Maynadié M , Staines A, Shield L, Lake A, Montgomery D, Taylor M, Smedby KE, Amini R-M, Adami H-O, Glimelius B, Feenstra B, and 40 others. Genome-wide Association Study of Classical Hodgkin Lymphoma and Epstein-Barr Virus Status-defined Subgroups. J National Cancer Institute 2012; 104: 240-253. PubMeddoi

Ryckman KK, Feenstra B, Shaffer JR, Bream ENA, Geller F, Feingold E, Weeks DE, Gadow E, Cosentino V, Saleme C, Simhan HN, Merrill D, Fong C-T, Busch T, Berends SK, Comas B, Camelo JL, Boyd HA, Laurie C, Crosslin D, Zhang Q, Doheny KF, Pugh E, Melbye M, Marazita ML, Dagle JM, Murray JC. Replication of a GenomeWide Association Study of Birth Weight in Preterm Neonates. J Pediatrics 2012; 160: 19-24. PubMeddoi

2011

Geller Fs, Feenstra Bs, Zhang H, Shaffer JR, Hansen T, Esserlind A-L, Boyd HA, Nohr EA, Timpson NJ, Fatemifar G, Paternoster L, Evans DM, Weyant RJ, Levy SM, Lathrop M, Smith GD, Murray JC, Olesen J, Werge T, Marazita ML, Sørensen TIA, Melbye M. Genome-Wide Association Study Identifies Four Loci Associated with Eruption of Permanent Teeth. PLoS Genetics 2011; 7: e1002275. PubMeddoi

Shaffer JR, Wang X, Feingold E, Lee M, Begum F, Weeks DE, Cuenco KT, Barmada MM, Wendell SK, Crosslin DR, Laurie CC, Doheny KF, Pugh EW, Zhang Q, Feenstra B, Geller F, Boyd HA, Zhang H, Melbye M, Murray JC, Weyant RJ, Crout R, McNeil DW, Levy SM, Slayton RL, Willing MC, Broffitt B, Vieira AR, Marazita ML. Genome-wide association scan for childhood caries implicates novel genes. J Dental Research 2011; 90: 1457-1462.PubMeddoi.

Yang J, Manolio TA, Pasquale LR, Boerwinkle E, Caporaso N, Cunningham JM, de Andrade M, Feenstra B, and 16 others. Genome-partitioning of genetic variation for complex traits using common SNPs. Nature Genetics 2011; 43: 519-525 PubMeddoi

Sulem P, Gudbjartsson DF, Geller F, Prokopenko I, Feenstra B, and 25 others. Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption. Human Molecular Genetics 2011; 20: 2071-2077. PubMeddoi.

2010

Elks CE, Perry FRB, Sulem P, Chasman DI, Franceschini N, He C, Lunetta KL, Visser JA, Byrne EM, Cousminer DL, Gudbjartsson DF, Esko T, Feenstra B, and 161 others. Thirty new loci for age at menarche identified by a meta-analysis of genomewide association studies. Nature Genetics 2010; 42:1077-1085. PubMeddoi

Greenberg DA, Monti MC, Feenstra B, Zhang J, Hodge SE. The essence of linkagebased imprinting detection: Comparing power, type 1 error, and the effects of confounders in two different analysis approaches. Ann Hum Genet. 2010; 74: 248-262. PubMeddoi

Cornelis MC, Agrawal A, Cole JW, Hansel NN, Barnes KC, Beaty TH, Bennett SN, Bierut LJ, Boerwinkle E, Doheny KF, Feenstra B, Feingold E, Fornage M, Haiman CA, Harris EL , Hayes MG, Heit JA, Hu FB, Kang JH, Laurie CC, Ling H, Manolio TA, Marazita ML, Mathias RA, Mirel DB, Paschall J, Pasquale LR, Pugh EW, Rice JP, Udren J, van Dam RM, Wang X, Wiggs JL, Williams K, Yu K for the GENEVA Consortium. The Gene, Environment Association Studies Consortium (GENEVA): Maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions. Genetic Epidemiology 2010; 34: 364-372. PubMed doi

2009

Boyd HA, Poulsen G, Wohlfahrt J, Murray JC, Feenstra B, Melbye M. Maternal contributions to preterm delivery. Am J Epidemiol. 2009; 170: 1358-64. PubMeddoi

Sulem P, Gudbjartsson DF, Rafnar T, Holm H, Olafsdottir EJ, Olafsdottir GH, Jonsson T, Alexandersen P, Feenstra B, Boyd HA, Aben KK, Verbeek AL, Roeleveld N, Jonasdottir A, Styrkarsdottir U, Steinthorsdottir V, Karason A, Stacey SN, Gudmundsson J, Jakobsdottir M, Thorleifsson G, Hardarson G, Gulcher J, Kong A, Kiemeney LA, Melbye M, Christiansen C, Tryggvadottir L, Thorsteinsdottir U, Stefansson K. Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche. Nature Genetics 2009; 41: 734-738. PubMeddoi

2008

Feenstra B, Boyd HA, Melbye M. [Genome-wide association studies]. Ugeskr Laeger 2008; 170: 3216-20 (Danish).

2006

Feenstra B, Skovgaard IM, Broman KW. Mapping quantitative trait loci by an extension of the Haley-Knott regression method using estimating equations. Genetics 2006; 173: 2269-2278. PubMeddoi

Christiansen MJ, Feenstra B, Skovgaard IM, Andersen SB. Genetic analysis of resistance to yellow rust in hexaploid wheat using multiple crosses. Theor. Appl. Genet. 2006; 112: 581-591. PubMeddoi

2004

Feenstra B, Skovgaard IM. A QTL mixture model that avoids spurious LOD score peaks. Genetics 2004; 167: 959-965 PubMeddoi

Feenstra B, Greenberg DA, Hodge SE. Using LOD scores to detect sex differences in male-female recombination fractions. Hum. Hered. 2004; 57: 100-108. PubMeddoi

1999

Armstrong DP, Castro I, Alley JC, Feenstra B, Perrott JK. Mortality and behaviour of Hihi, an endangered New Zealand honeyeater, in the establishment phase following translocation. Biol. Cons. 1999; 89: 329-339.

Letters

Njølstad PR, Feenstra B, Freathy RM. Regulation of placental growth is a complex interplay of maternal and fetal genomes. Nature Genetics 2023; 55:1786–1787. PubMed doi

Pasternak B, Feenstra B, Melbye M, Hviid A. Improving vaccine safety through a better understanding of vaccine adverse events. Clin. Infect. Dis. 2015; 60(10):1586-1587.

Geller F, Feenstra B, Melbye M. No association between sex ratio of offspring and the mother’s age at menarche (letter to the editor). Hum Reprod. 2011; 26: 3202-3203