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by Stitziel, Nathan O and Stirrups, Kathleen E and Masca, Nicholas G D and Erdmann, Jeanette and Ferrario, Paola G and König, Inke R and Weeke, Peter E and Webb, Thomas R and Auer, Paul L and Schick, Ursula M and Lu, Yingchang and Zhang, He and Dube, Marie-Pierre and Goel, Anuj and Farrall, Martin and Peloso, Gina M and Won, Hong-Hee and Do, Ron and van Iperen, Erik and Kanoni, Stavroula and Kruppa, Jochen and Mahajan, Anubha and Scott, Robert A and Willenberg, Christina and Braund, Peter S and van Capelleveen, Julian C and Doney, Alex S F and Donnelly, Louise A and Asselta, Rosanna and Merlini, Piera A and Duga, Stefano and Marziliano, Nicola and Denny, Josh C and Shaffer, Christian M and El-Mokhtari, Nour Eddine and Franke, Ane and Gottesman, Omri and Heilmann, Stefanie and Hengstenberg, Christian and Hoffman, Per and Holmen, Oddgeir L and Hveem, Kristian and Jansson, Jan-Håkan and Jöckel, Karl-Heinz and Kessler, Thorsten and Kriebel, Jennifer and Laugwitz, Karl L and Marouli, Eirini and Martinelli, Nicola and McCarthy, Mark I and Van Zuydam, Natalie R and Meisinger, Christa and Esko, Tõnu and Mihailov, Evelin and Escher, Stefan A and Alvar, Maris and Moebus, Susanne and Morris, Anew D and Müller-Nurasyid, Martina and Nikpay, Majid and Olivieri, Oliviero and Lemieux Perreault, Louis-Philippe and AlQarawi, Alaa and Robertson, Neil R and Akinsanya, Karen O and Reilly, Dermot F and Vogt, Thomas F and Yin, Wu and Asselbergs, Folkert W and Kooperberg, Charles and Jackson, Rebecca D and Stahl, Eli and Strauch, Konstantin and Varga, Tibor V and Waldenberger, Melanie and Zeng, Lingyao and Kraja, Aldi T and Liu, Chunyu and Ehret, George B and Newton-Cheh, Christopher and Chasman, Daniel I and Chowdhury, Rajiv and Ferrario, Marco and Ford, Ian and Jukema, J Wouter and Kee, Frank and Kuulasmaa, Kari and Nordestgaard, Børge G and Perola, Markus and Saleheen, Danish and Sattar, Naveed and Surenan, Praveen and Tregouet, David and Young, Robin and Howson, Joanna M M and Butterworth, Adam S and Danesh, John and Ardissino, Diego and Bottinger, Erwin P and Erbel, Raimund and ... and Diabetes - kardiovaskulär sjukdom and Kardiovaskulär forskning - hypertoni and Cardiovascular Research - Hypertension and Kansli för kliniska vetenskaper, Lund and EpiHealth: Epidemiology for Health and Institutionen för kliniska vetenskaper, Malmö and Genetisk och molekylär epidemiologi and Lunds universitet and Diabetes - Cardiovascular Disease and Lund University and Department Office of Clinical Sciences, Lund and Genetic and Molecular Epidemiology and EXODIAB: Excellence in Diabetes Research in Sweden and Department of Clinical Sciences, Malmö
New England Journal of Medicine, ISSN 0028-4793, 02/2016, Volume 374, Issue 12, p. 1134
BACKGROUND: The discovery of low-frequency coding variants affecting the risk of coronary artery disease has facilitated the identification of therapeutic... 
Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
by Stitziel, Nathan O and Stirrups, Kathleen E and Masca, Nicholas G. D and Erdmann, Jeanette and Ferrario, Paola G and König, Inke R and Weeke, Peter E and Webb, Thomas R and Auer, Paul L and Schick, Ursula M and Lu, Yingchang and Zhang, He and Dube, Marie-Pierre and Goel, Anuj and Farrall, Martin and Peloso, Gina M and Won, Hong-Hee and Do, Ron and van Iperen, Erik and Kanoni, Stavroula and Kruppa, Jochen and Mahajan, Anubha and Scott, Robert A and Willenborg, Christina and Braund, Peter S and van Capelleveen, Julian C and Doney, Alex S. F and Donnelly, Louise A and Asselta, Rosanna and Merlini, Piera A and Duga, Stefano and Marziliano, Nicola and Denny, Josh C and Shaffer, Christian M and El-Mokhtari, Nour Eddine and Franke, Ane and Gottesman, Omri and Heilmann, Stefanie and Hengstenberg, Christian and Hoffmann, Per and Holmen, Oddgeir L and Hveem, Kristian and Jansson, Jan-Håkan and Jöckel, Karl-Heinz and Kessler, Thorsten and Kriebel, Jennifer and Laugwitz, Karl L and Marouli, Eirini and Martinelli, Nicola and McCarthy, Mark I and van Zuydam, Natalie R and Meisinger, Christa and Esko, Tõnu and Mihailov, Evelin and Escher, Stefan A and Alver, Maris and Moebus, Susanne and Morris, Anew D and Müller-Nurasyid, Martina and Nikpay, Majid and Olivieri, Oliviero and Perreault, Louis-Philippe Lemieux and AlQarawi, Alaa and Robertson, Neil R and Akinsanya, Karen O and Reilly, Dermot F and Vogt, Thomas F and Yin, Wu and Asselbergs, Folkert W and Kooperberg, Charles and Jackson, Rebecca D and Stahl, Eli and Strauch, Konstantin and Varga, Tibor V and Waldenberger, Melanie and Zeng, Lingyao and Kraja, Aldi T and Liu, Chunyu and Ehret, Georg B and Newton-Cheh, Christopher and Chasman, Daniel I and Chowdhury, Rajiv and Ferrario, Marco and Ford, Ian and Jukema, J. Wouter and Kee, Frank and Kuulasmaa, Kari and Nordestgaard, Børge G and Perola, Markus and Saleheen, Danish and Sattar, Naveed and Surenan, Praveen and Tregouet, David and Young, Robin and Howson, Joanna M. M and Butterworth, Adam S and Danesh, John and Ardissino, Diego and Bottinger, Erwin P and Erbel, Raimund and ... and Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Umeå universitet and Medicin
The New England Journal of Medicine, ISSN 0028-4793, 03/2016, Volume 374, Issue 12, pp. 1134 - 1144
Journal Article
Bioinformatics, ISSN 1367-4803, 2016, Volume 32, Issue 23, pp. 3661 - 3663
Genotype imputation is now commonly performed following genome-wide genotyping experiments. Imputation increases the density of analyzed genotypes in the... 
BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ASSOCIATION | BIOCHEMICAL RESEARCH METHODS | MATHEMATICAL & COMPUTATIONAL BIOLOGY | Computational Biology - methods | Humans | Genotype | Software | Genome | Genomics - methods | Automatic Data Processing | Applications Notes
Journal Article
PLoS Genetics, ISSN 1553-7390, 09/2012, Volume 8, Issue 9, p. e1002903
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 6, pp. 629 - 634
Journal Article
Epigenetics and Chromatin, ISSN 1756-8935, 06/2016, Volume 9, Issue 1, p. 25
Background: Prenatal alcohol exposure is the leading preventable cause of behavioral and cognitive deficits, which may affect between 2 and 5 % of children in... 
METAANALYSIS | TISSUE | REGIONS | GENETICS & HEREDITY | GENE-EXPRESSION | ISLANDS | EXPOSURE | CONSUMPTION | BRAIN | INSIGHTS | FEATURES | Fetal alcohol syndrome | Epigenetic inheritance | Analysis | Genomics | Effect of alcohol on | Fetus | Genetic aspects | Research | Diagnosis
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2017, Volume 12, Issue 4, p. e0174783
Background In the Western world, between 1940 and 1970, more than 2 million people were exposed in utero to diethylstilbestrol (DES). In exposed individuals,... 
IN-UTERO | DEVELOPMENTAL NEUROTOXICITY | NEONATAL EXPOSURE | DNA METHYLATION | SEXUAL-DIFFERENTIATION | MULTIDISCIPLINARY SCIENCES | EMBRYONIC STEM-CELLS | SPECTRUM DISORDERS | GENE FAMILY | BISPHENOL-A | EPIGENETIC CHANGES | Promoter Regions, Genetic | Epigenesis, Genetic | Humans | Male | Prenatal Exposure Delayed Effects - physiopathology | Prenatal Exposure Delayed Effects - metabolism | DNA-Binding Proteins - metabolism | Pregnancy | Psychotic Disorders - metabolism | Transcription Factors - metabolism | DNA Methylation | ADAMTS9 Protein - metabolism | CpG Islands | Maternal Exposure - adverse effects | Adult | Female | Diethylstilbestrol - toxicity | Prenatal Exposure Delayed Effects - chemically induced | Psychotic Disorders - etiology | Diethylstilbestrol | Research | Psychoses | Methylation | Risk factors | Adenocarcinoma | Heart | Brain | Parkinson's disease | Estrogens | Embryo cells | Bipolar disorder | Hormones | Blood | Alterations | Prenatal experience | Movement disorders | Deoxyribonucleic acid--DNA | Immunoglobulins | Immunization | Neurodegenerative diseases | Vagina | Rats | Exposure | Gene expression | Metabolism | Fatty acids | Studies | Mounting | Offspring | Millet | Stem cells | Monoclonal antibodies | Adults | Mice | Aberration | Hippocampus | Anomalies | Endocrine disruptors | Haplotypes | Animal models | Mental disorders | Change detection | Genes | Homeostasis | Risk | Windows (intervals) | Immunology | Uterus | Imprinting | DNA methylation | Children | Siblings | Immune system | Immune response | Neurons | Complications | Pharmacology | Conspecifics | Cervix | Cell differentiation | Autism | Human rights | Womens health | Epigenetics | Differentiation | Psychiatry | Cancer | Life Sciences | Human health and pathology | Psychiatrics and mental health | Deoxyribonucleic acid | DNA
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 2014, Volume 23, Issue 12, pp. 3316 - 3326
Journal Article