CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer

por Margolin, Sara, Eiberg, Hans, Lindblom, Annika, Bisgaard, Marie Luise
Publicado 2007

Polymorphisms in Phase I and Phase II genes and breast cancer risk and relations to persistent organic pollutant exposure: a case–control study in Inuit women

por Ghisari, Mandana, Eiberg, Hans, Long, Manhai, Bonefeld-Jørgensen, Eva C
Publicado 2014

A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family

por Anjum, Iram, Eiberg, Hans, Baig, Shahid Mahmood, Tommerup, Niels, Hansen, Lars
Publicado 2010

Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study

por Hollensted, Mette, Ekstrøm, Claus T., Pedersen, Oluf, Eiberg, Hans, Hansen, Torben, Gjesing, Anette Prior
Publicado 2018

High brain serotonin levels in migraine between attacks: A 5-HT(4) receptor binding PET study

por Deen, Marie, Hansen, Hanne D., Hougaard, Anders, Nørgaard, Martin, Eiberg, Hans, Lehel, Szabolcs, Ashina, Messoud, Knudsen, Gitte M.
Publicado 2018

Associations of the Inflammatory Marker YKL-40 with Measures of Obesity and Dyslipidaemia in Individuals at High Risk of Type 2 Diabetes

por Thomsen, Stine B., Gjesing, Anette P., Rathcke, Camilla N., Ekstrøm, Claus T., Eiberg, Hans, Hansen, Torben, Pedersen, Oluf, Vestergaard, Henrik
Publicado 2015

Dominant optic atrophy in Denmark – report of 15 novel mutations in OPA1, using a strategy with a detection rate of 90%

por Almind, Gitte J, Ek, Jakob, Rosenberg, Thomas, Eiberg, Hans, Larsen, Michael, LuCamp, LuCamp, Brøndum-Nielsen, Karen, Grønskov, Karen
Publicado 2012

Novel de novo BRCA2 mutation in a patient with a family history of breast cancer

por Hansen, Thomas V O, Bisgaard, Marie Luise, Jønson, Lars, Albrechtsen, Anders, Filtenborg-Barnkob, Bettina, Eiberg, Hans, Ejlertsen, Bent, Nielsen, Finn C
Publicado 2008

A splice-site variant in the lncRNA gene RP1-140A9.1 cosegregates in the large Volkmann cataract family

por Eiberg, Hans, Mikkelsen, Annemette F., Bak, Mads, Tommerup, Niels, Lund, Allan M., Wenzel, Anne, Sabarinathan, Radhakrishnan, Gorodkin, Jan, Bang-Berthelsen, Claus H., Hansen, Lars
Publicado 2019

Variants Near MC4R Are Associated With Obesity and Influence Obesity-Related Quantitative Traits in a Population of Middle-Aged People: Studies of 14,940 Danes

por Zobel, Dorit P., Andreasen, Camilla H., Grarup, Niels, Eiberg, Hans, Sørensen, Thorkild I.A., Sandbæk, Annelli, Lauritzen, Torsten, Borch-Johnsen, Knut, Jørgensen, Torben, Pedersen, Oluf, Hansen, Torben
Publicado 2009

Blood-based biomarkers of age-associated epigenetic changes in human islets associate with insulin secretion and diabetes

por Bacos, Karl, Gillberg, Linn, Volkov, Petr, Olsson, Anders H, Hansen, Torben, Pedersen, Oluf, Gjesing, Anette Prior, Eiberg, Hans, Tuomi, Tiinamaija, Almgren, Peter, Groop, Leif, Eliasson, Lena, Vaag, Allan, Dayeh, Tasnim, Ling, Charlotte
Publicado 2016

Paroxysmal Cranial Dyskinesia and Nail‐Patella Syndrome Caused by a Novel Variant in the LMX1B Gene

por Bech, Sara, Løkkegaard, Annemette, Nielsen, Troels T., Nørremølle, Anne, Grønborg, Sabine, Hasholt, Lis, Steffensen, Gudrun K., Graehn, Gabor, Olesen, Jess H., Tommerup, Niels, Mang, Yuan, Bak, Mads, Nielsen, Jørgen E., Eiberg, Hans, Hjermind, Lena E.
Publicado 2020

Epigenetic remodelling and dysregulation of DLGAP4 is linked with early-onset cerebellar ataxia

por Minocherhomji, Sheroy, Hansen, Claus, Kim, Hyung-Goo, Mang, Yuan, Bak, Mads, Guldberg, Per, Papadopoulos, Nickolas, Eiberg, Hans, Doh, Gerald Dayebga, Møllgård, Kjeld, Hertz, Jens Michael, Nielsen, Jørgen E., Ropers, Hans-Hilger, Tümer, Zeynep, Tommerup, Niels, Kalscheuer, Vera M., Silahtaroglu, Asli
Publicado 2014

Genetic Correlation between Body Fat Percentage and Cardiorespiratory Fitness Suggests Common Genetic Etiology

por Schnurr, Theresia M., Gjesing, Anette P., Sandholt, Camilla H., Jonsson, Anna, Mahendran, Yuvaraj, Have, Christian T., Ekstrøm, Claus T., Bjerregaard, Anne-Louise, Brage, Soren, Witte, Daniel R., Jørgensen, Marit E., Aadahl, Mette, Thuesen, Betina H., Linneberg, Allan, Eiberg, Hans, Pedersen, Oluf, Grarup, Niels, Kilpeläinen, Tuomas O., Hansen, Torben
Publicado 2016

Family and Population-Based Studies of Variation within the Ghrelin Receptor Locus in Relation to Measures of Obesity

por Gjesing, Anette P., Larsen, Lesli H., Torekov, Signe S., Hainerová, Irena Aldhoon, Kapur, Rahul, Johansen, Anders, Albrechtsen, Anders, Boj, Sylvia, Holst, Birgitte, Harper, Angela, Urhammer, Søren A., Borch-Johnsen, Knut, Pisinger, Charlotta, Echwald, Søren M., Eiberg, Hans, Astrup, Arne, Lebl, Jan, Ferrer, Jorge, Schwartz, Thue W., Hansen, Torben, Pedersen, Oluf
Publicado 2010

RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesis

por Farooq, Muhammad, Lindbæk, Louise, Krogh, Nicolai, Doganli, Canan, Keller, Cecilie, Mönnich, Maren, Gonçalves, André Brás, Sakthivel, Srinivasan, Mang, Yuan, Fatima, Ambrin, Andersen, Vivi Søgaard, Hussain, Muhammad S., Eiberg, Hans, Hansen, Lars, Kjaer, Klaus Wilbrandt, Gopalakrishnan, Jay, Pedersen, Lotte Bang, Møllgård, Kjeld, Nielsen, Henrik, Baig, Shahid. M., Tommerup, Niels, Christensen, Søren Tvorup, Larsen, Lars Allan
Publicado 2020

Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios

por Besenbacher, Søren, Liu, Siyang, Izarzugaza, José M. G., Grove, Jakob, Belling, Kirstine, Bork-Jensen, Jette, Huang, Shujia, Als, Thomas D., Li, Shengting, Yadav, Rachita, Rubio-García, Arcadio, Lescai, Francesco, Demontis, Ditte, Rao, Junhua, Ye, Weijian, Mailund, Thomas, Friborg, Rune M., Pedersen, Christian N. S., Xu, Ruiqi, Sun, Jihua, Liu, Hao, Wang, Ou, Cheng, Xiaofang, Flores, David, Rydza, Emil, Rapacki, Kristoffer, Damm Sørensen, John, Chmura, Piotr, Westergaard, David, Dworzynski, Piotr, Sørensen, Thorkild I. A., Lund, Ole, Hansen, Torben, Xu, Xun, Li, Ning, Bolund, Lars, Pedersen, Oluf, Eiberg, Hans, Krogh, Anders, Børglum, Anders D., Brunak, Søren, Kristiansen, Karsten, Schierup, Mikkel H., Wang, Jun, Gupta, Ramneek, Villesen, Palle, Rasmussen, Simon
Publicado 2015

A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants

por Wood, Andrew R., Jonsson, Anna, Jackson, Anne U., Wang, Nan, van Leewen, Nienke, Palmer, Nicholette D., Kobes, Sayuko, Deelen, Joris, Boquete-Vilarino, Lorena, Paananen, Jussi, Stančáková, Alena, Boomsma, Dorret I., de Geus, Eco J.C., Eekhoff, Elisabeth M.W., Fritsche, Andreas, Kramer, Mark, Nijpels, Giel, Simonis-Bik, Annemarie, van Haeften, Timon W., Mahajan, Anubha, Boehnke, Michael, Bergman, Richard N., Tuomilehto, Jaakko, Collins, Francis S., Mohlke, Karen L., Banasik, Karina, Groves, Christopher J., McCarthy, Mark I., Pearson, Ewan R., Natali, Andrea, Mari, Andrea, Buchanan, Thomas A., Taylor, Kent D., Xiang, Anny H., Gjesing, Anette P., Grarup, Niels, Eiberg, Hans, Pedersen, Oluf, Chen, Yii-Derr, Laakso, Markku, Norris, Jill M., Smith, Ulf, Wagenknecht, Lynne E., Baier, Leslie, Bowden, Donald W., Hansen, Torben, Walker, Mark, Watanabe, Richard M., ‘t Hart, Leen M., Hanson, Robert L., Frayling, Timothy M.
Publicado 2017