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article; body height; brain growth; child; chromosome 12q; chromosome 12q15; chromosome 12q24; degenerative disease; disease association; female; gene locus; genetic association; genetic variability; head circumference; human; infant; infant head circumference; male; meta analysis; parkinson disease; preschool child; priority journal; single nucleotide polymorphism (1) 1
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JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2016, Volume 68, Issue 16, pp. 1765 - 1768
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2014, Volume 63, Issue 14, pp. 1430 - 1437
Journal Article
by Traylor, Matthew, MSc and Farrall, Martin, FRCPath and Holliday, Elizabeth G, PhD and Sudlow, Cathie, FRCP and Hopewell, Jemma C, PhD and Cheng, Yu-Ching, PhD and Fornage, Myriam, PhD and Ikram, M Arfan, MD and Malik, Rainer, PhD and Bevan, Steve, PhD and Thorsteinsdottir, Unnur, PhD and Nalls, Mike A, PhD and Longstreth, WT, MD and Wiggins, Kerri L, MS and Yadav, Sunaina, MSc and Parati, Eugenio A, MD and DeStefano, Anita L, PhD and Worrall, Bradford B, MD and Kittner, Steven J, MD and Khan, Muhammad Saleem, MSc and Reiner, Alex P, MD and Helgadottir, Anna, MD and Achterberg, Sefanja, PhD and Fernandez-Cadenas, Israel, PhD and Abboud, Sherine, MD and Schmidt, Reinhold, MD and Walters, Matthew, MD and Chen, Wei-Min, PhD and Ringelstein, E Bernd, MD and O'Donnell, Martin, MD and Ho, Weang Kee, PhD and Pera, Joanna, MD and Lemmens, Robin, MD and Norrving, Bo, MD and Higgins, Peter, MRCP and Benn, Marianne, MD and Sale, Michele, PhD and Kuhlenbäumer, Gregor, MD and Doney, Alexander S F, PhD and Vicente, Astrid M, PhD and Delavaran, Hossein, MD and Algra, Ale, MD and Davies, Gail, PhD and Oliveira, Sofia A, PhD and Palmer, Colin N A, PhD and Deary, Ian, PhD and Schmidt, Helena, MD and Pandolfo, Massimo, MD and Montaner, Joan, MD and Carty, Cara, PhD and de Bakker, Paul I W, PhD and Kostulas, Konstantinos, MD and Ferro, Jose M, MD and van Zuydam, Natalie R, MSc and Valdimarsson, Einar, MD and Nordestgaard, Børge G, MD and Lindgren, Arne, MD and Thijs, Vincent, MD and Slowik, Agnieszka, MD and Saleheen, Danish, MD and Paré, Guillaume, MD and Berger, Klaus, MD and Thorleifsson, Gudmar, PhD and Hofman, Albert, MD and Mosley, Thomas H, PhD and Mitchell, Braxton D, PhD and Furie, Karen, MD and Clarke, Robert, FRCP and Levi, Christopher, MD and Seshadri, Sudha, MD and Gschwendtner, Andreas, MD and Boncoraglio, Giorgio B, MD and Sharma, Pankaj, PhD and Bis, Joshua C, PhD and Gretarsdottir, Solveig, PhD and Psaty, Bruce M and Rothwell, Peter M, FMedSci and Rosand, Jonathan, MD and Meschia, James F, MD and Stefansson, Kari, MD and Dichgans, Martin, MD and Markus, Hugh S, Dr and WTCCC 2 and Australian Stroke Genetics Collabo and Int Stroke Genetics Consortium and International Stroke Genetics Consortium and Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) and EpiHealth: Epidemiology for Health and Lund University and Neurologi, Lund and Neurology, Lund and Lunds universitet
The Lancet Neurology, ISSN 1474-4422, 2012, Volume 11, Issue 11, pp. 951 - 962
Journal Article
American Heart Journal, ISSN 0002-8703, 2015, Volume 169, Issue 5, pp. 631 - 638.e7
Journal Article
by Taal, Rob and St Pourcain, Beate and Thiering, Eelisabeth and Das, Shikta and Mook-Kanamori, Dennis and Warrington, Nicole and Kaakinen, Marika and Kreiner-Møller, Eskil and Bradfield, Jonathan and Freathy, Rachel and Geller, Frank and Guxens Junyent, Mònica and Cousminer, Diana and Kerkhof, Marjan and Timpson, Nicholas and Ikram, Arfan and Beilin, Lawrence and Bønnelykke, Klaus and Buxton, Jessica and Charoen, Pimphen and Chawes, Bo Lund Krogsgaard and Eriksson, Johan and Evans, David and Hofman, Albert and Kemp, John and Kim, Cecilia and Klopp, Norman and Lahti, Jari and Lye, Stephen and Mcmahon, George and Mentch, Frank and Müller-Nurasyid, Martina and O'Reilly, Paul and Prokopenko, Inga and Rivadeneira Ramirez, Fernando and Steegers, Eric and Sunyer, Jordi and Tiesler, Carla and Yaghootkar, Hanieh and Breteler, Monique and Debette, Stéphanie and Fornage, Myriam and Gudnason, Vilmunder and Launer, Lenore and Lugt, Aad and Mosley, Thomas and Seshai, Sudha and Smith, Albert V and Vernooij, Meike and Blakemore, Alexana and Chiavacci, Rosetta and Feenstra, Bjarke and Fernandez-Banet, Julio and Grant, Struan and Hartikainen, Anna-Liisa and Heijden, Albert and Iniguez, Carmen and Lathrop, Mark and McArdle, Wendy and Mølgaard, Anne and Newnham, John and Palmer, Lyle and Palotie, Aarno and Pouta, Anneli and Ring, Susan and Sovio, Ulla and Standl, Marie and Uitterlinden, Ané and Wichmann, Erich and Vissing, Nadja and DeCarli, Charles and Duijn, Cornelia and McCarthy, M and Koppelman, Gerard and Estivill, Xavier and Hattersley, Anew and Melbye, Mads and Bisgaard, Hans and Pennell, Craig and Widen, Elisabeth and Hakonarson, Hakon and Davey-Smith, George and Heinrich, Joachim and Jarvelin, Marjo-Riitta and Jaddoe, Vincent and Cohorts Heart Aging Res Genetic Ep and Early Genetics Lifecourse Epidemio and Early Growth Genetics EGG Consorti and Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium and Early Genetics & Lifecourse Epidemiology (EAGLE) consortium and Early Growth Genetics (EGG) Consortium and Early Genetics & Lifecourse Epidemiology (EAGLE) Consortium and The Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium and Mittuniversitetet and Institutionen för samhällsvetenskap and Fakulteten för humanvetenskap
Nature Genetics, ISSN 1061-4036, 05/2012, Volume 44, Issue 5, pp. 532 - 538
textabstractTo identify genetic variants associated with head circumference in infancy, we performed a meta-analysis of seven genome-wide association studies... 
INTELLIGENCE | PROTEIN | GENE | FETAL-GROWTH | GENETICS & HEREDITY | BRAIN-DEVELOPMENT | DISORDERS | MUTATIONS | IDENTIFICATION | GENOME-WIDE ASSOCIATION | PARKINSONS-DISEASE | Pregnancy Complications - pathology | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Meta-Analysis as Topic | Pregnancy Complications - etiology | Humans | Infant | Male | Head - growth & development | Genetic Loci | Genetic Markers | Head - pathology | Pregnancy | Polymorphism, Single Nucleotide - genetics | Female | Chromosomes, Human, Pair 12 - genetics | Head | Genetic aspects | Genetic variation | Identification and classification | Body size | Confidence intervals | Medical research | Brain | Breastfeeding & lactation | Health services | Prenatal development | Genetics | Epidemiology | Meta-analysis | Malalties | Creixement | Polimorfisme genètic | Cap | Complicacions | Cromosomes humans | Embaràs | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | article; body height; brain growth; child; chromosome 12q; chromosome 12q15; chromosome 12q24; degenerative disease; disease association; female; gene locus; genetic association; genetic variability; head circumference; human; infant; infant head circumference; male; meta analysis; Parkinson disease; preschool child; priority journal; single nucleotide polymorphism
Journal Article
by Jun, Yang and Ibrahim-Verbaas, Carla and Vronskaya, M and Lambert, J.-C and Chung, J and Naj, Adam and Kunkle, Brian and Wang, L.-S and Bis, Joshua and Bellenguez, Céline and Harold, Denise and Lunetta, Kathryn and DeStefano, Anita L and Grenier-Boley, Benjamin and Sims, Rebecca and Beecham, G.W and Smith, Albert and Chouraki, Vincent and Hamilton-Nelson, Kara and Ikram, Arfan and Fiévet, Nathalie and Denning, Nicola and Martin, E.R and Schmidt, H and Kamatani, Y and Dunstan, M.L and Valladares, Otto and Laza, A.R and Zelenika, Diana and Ramirez, Alfredo and Foroud, Tatiana and Choi, Seung-Hoan and Boland, A and Becker, T and Kukull, W.A and Lee, Sven and Pasquier, Florence and Cruchaga, Carlos and Beekly, Duane and Fitzpatrick, Annette and Hanon, Olivier and Gill, M and Barber, Rachel and Gudnason, Vilmundur and Campion, D and Love, S and Bennett, David A and Amin, Najaf and Berr, Claudine and Tsolaki, Magda and Buxbaum, J.D and Lopez, O.L and Deramecourt, Vincent and Fox, N.C and Cantwell, Laura B and Tárraga, L and Dufouil, Carole and Hardy, J and Crane, L.M.A and Eiriksdottir, Gudny and Hannequin, Didier and Clarke, Robert and Evans, D and Mosley, Thomas H and Letenneur, L and Brayne, Carol and Maier, W and De Jager, P and Emilsson, Valur and Dartigues, Jean-François and Hampel, H and Kamboh, M. Ilyas and Bruijn, Renée and Tzourio, Christophe and Pastor, Pau and Larson, Eric B and Rotter, J.I and O'donovan, Michael and Montine, Thomas J and Nalls, Michael and Mead, Simon and Reiman, Eric and Jonsson, P.V and Holmes, C and St George-Hyslop, P.H and Boada, Mercè and Passmore, Peter and Wendland, Annika and Schmidt, R and Morgan, Kevin and Winslow, A.R and Powell, J.F and Carasquillo, M and Younkin, S and Jakobsdottir, Margret and Kauwe, J.S.K and Wilhelmsen, K.C and Rujescu, Dan and Nöthen, Markus M and Hofman, Albert and ... and IGAP Consortium
Molecular Psychiatry, ISSN 1359-4184, 01/2016, Volume 21, Issue 1, pp. 108 - 117
Journal Article