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Nature Communications, ISSN 2041-1723, 12/2019, Volume 10, Issue 1, pp. 1054 - 17
While genetic variation at chromatin loops is relevant for human disease, the relationships between contact propensity (the probability that loci at loops... 
ORGANIZATION | ACTIVATION | BIOCONDUCTOR PACKAGE | 3D GENOME | RECONSTRUCTION | MULTIDISCIPLINARY SCIENCES | ARCHITECTURE | PROVIDES | DOMAINS | PRINCIPLES | REVEALS
Journal Article
Nature Genetics, ISSN 1061-4036, 10/2019, Volume 51, Issue 10, pp. 1506 - 1517
The cardiac transcription factor (TF) gene NKX2-5 has been associated with electrocardiographic (EKG) traits through genomewide association studies (GWASs),... 
Genome-wide association studies | Usage | Transcription factors | Electrocardiogram | Heart cells | Electrocardiography | Research | Heart | Binding | EKG | Phenotypes | Echocardiography | Principal components analysis | Cardiomyocytes | Genomes | Mapping | Nucleotides | Gene expression | Datasets | Quantitative trait loci | Stem cells | Alleles | Gene mapping | Bioinformatics | Pluripotency | Nkx2.5 protein | Deoxyribonucleic acid--DNA
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 05/2012, Volume 59, Issue 22, pp. 1928 - 1937
Journal Article
Neurosurgical focus, ISSN 1092-0684, 09/2018, Volume 45, Issue 3, p. E1
Journal Article
Neurosurgical Focus, 09/2018, Volume 45, Issue 3
Journal Article
by Ligthart, Symen and Vaez, Ahmad and Võsa, Urmo and Stathopoulou, Maria G and Stathopoulou, Maria and de Vries, Paul S and Prins, Bram P and Prins, Bram and Van der Most, Peter J and Tanaka, Toshiko and Naderi, Elnaz and Rose, Lynda M and Wu, Ying and Karlsson, Robert and Karlsson, Magnus and Barbalic, Maja and Lin, Honghuang and Pool, René and Zhu, Gu and Macé, Aurélien and Sidore, Carlo and Trompet, Stella and Mangino, Massimo and Sabater-Lleal, Maria and Kemp, John P and Abbasi, Ali and Kacprowski, Tim and Verweij, Niek and Smith, Albert V and Smith, Erin N and Smith, George Davey and Huang, Jie and Huang, Tao and Huang, Hongyan and Marzi, Carola and Feitosa, Mary F and Lohman, Kurt K and Kleber, Marcus E and Milaneschi, Yuri and Mueller, Christian and Huq, Mahmudul and Vlachopoulou, Efthymia and Lyytikäinen, Leo-Pekka and Oldmeadow, Christopher and Deelen, Joris and Perola, Markus and Zhao, Jing Hua and Zhao, Jing and Feenstra, Bjarke and Alizadeh, Behrooz Z and Boezen, H. Marike and Franke, Lude and van der Harst, Pim and Navis, Gerjan and Rots, Marianne and Snieder, Harold and Swertz, Morris and Wolffenbuttel, Bruce H.R and Wijmenga, Cisca and Amini, Marzyeh and Benjamin, Emelia J and Benjamin, Emelia and Chasman, Daniel I and Dehghan, Abbas and Ahluwalia, Tarunveer Singh and Ahluwalia, Tarunveer S and Meigs, James and Tracy, Russell and Tracy, Russell P and Bis, Josh and Bis, Joshua C and Eiriksdottir, Gudny and Pankratz, Nathan and Gross, Myron and Rainer, Alex and Wilson, James G and Wilson, James F and Psaty, Bruce M and Dupuis, Josee and Dupuis, Josée and Vaso, Urmo and Lehtimaki, Terho and Koenig, Wolfgang and Jamshidi, Yalda and Siest, Sophie and Uitterlinden, André G and Uitterlinden, Andre G and Abdollahi, Mohammadreza and Schnabel, Renate and Schick, Ursula M and Nolte, Ilja M and Kraja, Aldi and Hsu, Yi-Hsiang and Tylee, Daniel S and Zwicker, Alyson and Uher, Rudolf and Davey-Smith, George and Morrison, Alanna C and Hicks, Andrew and Hicks, Andrew A and ... and CHARGE Inflammation Working Grp and LifeLines Cohort Study and CHARGE Inflammation Working Group and Stockholms universitet and Numerisk analys och datalogi (NADA) and Naturvetenskapliga fakulteten
The American Journal of Human Genetics, ISSN 0002-9297, 11/2018, Volume 103, Issue 5, pp. 691 - 706
Journal Article
Haematologica, ISSN 0390-6078, 10/2019, p. haematol.2019.224279
Journal Article
Genetic Epidemiology, ISSN 0741-0395, 06/2019, Volume 43, Issue 4, pp. 449 - 457
Although recent Genome‐Wide Association Studies have identified novel associations for common variants, there has been no comprehensive exome‐wide search for... 
genetic association | venous thromboembolism | exome | VARIANTS | RARE | CODING VARIATION | LOW-FREQUENCY | RISK | BLOOD-PRESSURE | BREAST-CANCER | PULMONARY-EMBOLISM | GENETICS & HEREDITY | MATHEMATICAL & COMPUTATIONAL BIOLOGY | CORONARY-HEART-DISEASE | GENOME-WIDE ASSOCIATION | African Americans | Fibrin | Thromboembolism | Analysis | Genomics | ABO system | Genomes | Gene frequency | Health risk assessment | Alleles
Journal Article
Neurosurgical Focus, ISSN 1092-0684, 10/2019, Volume 47, Issue 4, p. E1
Journal Article
Infant Behavior and Development, ISSN 0163-6383, 11/2019, Volume 57, p. 101378
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 05/2019, Volume 179, Issue 5, pp. 762 - 769
This study explored patients' experiences and perceptions of living with thalassemia (an inherited hematologic disorder), perceptions of social stigma, and... 
thalassemia major | Southeast Asia | stigma | genetic condition | disclosure decision making | Thalassemia | Families & family life | Decision making
Journal Article
Stem cell reports, ISSN 2213-6711, 06/2019, Volume 12, Issue 6, pp. 1342 - 1353
We evaluate whether human induced pluripotent stem cell-derived retinal pigment epithelium (iPSC-RPE) cells can be used to prioritize and functionally... 
Journal Article
Cancer Epidemiology Biomarkers & Prevention, ISSN 1055-9965, 11/2014, Volume 23, Issue 11 Supplement, pp. A19 - A19
Journal Article
by Lee, Shermin and Ripke, S and Neale, B.M and Faraone, S.V and Purcell, S.M and Perlis, R.H and Mowry, B.J and Thapar, A and Goddard, M.E and Witte, J.S and Absher, D and Agartz, I and Akil, H and Amin, F and Aneassen, O.A and Anjorin, A and Anney, R and Anttila, V and Arking, D.E and Asherson, P and Azevedo, M.H and Backlund, L and Badner, J.A and Bailey, A.J and Banaschewski, T and Barchas, J.D and Barnes, M.R and Barrett, T.B and Bass, N and Battaglia, A and Bauer, M and Bayes, M and Bellivier, F and Bergen, S.E and Berrettini, W and Betancur, C and Bettecken, T and Biederman, J and Binder, E.B and Black, D.W and Blackwood, D.H and Bloss, C.S and Boehnke, M and Boomsma, D.I and Breen, G and Breuer, R and Bruggeman, R and Cormican, P and Buccola, N.G and Buitelaar, J.K and Bunney, W.E and Buxbaum, J.D and Byerley, W.F and Byrne, E.M and Caesar, S and Cahn, W and Cantor, R.M and Casas, M and Chakravarti, A and Chambert, K and Choudhury, K and Cichon, S and Cloninger, C.R and Collier, D.A and Cook, E.H and Coon, H and Cormand, B and Corvin, A and Coryell, W.H and Craig, D.W and Craig, I.W and Crosbie, J and Cuccaro, M.L and Curtis, D and Czamara, D and Datta, S and Dawson, G and Day, R and Geus, E.J. de and Degenhardt, F and Djurovic, S and Donohoe, G.J and Doyle, A.E and Duan, J and Dudbridge, F and Duketis, E and Ebstein, R.P and Edenberg, H.J and Elia, J and Ennis, S and Etain, B and Fanous, A and Farmer, A.E and Ferrier, I.N and Flickinger, M and Fombonne, E and Foroud, T and Frank, J and Franke, B and et al and Cross-Disorder Grp Psychiat Genomi and Int Inflammatory Bowel Dis Genetic and Cross-Disorder Group of the Psychiatric Genomics Consortium
Nature Genetics, ISSN 1061-4036, 2013, Volume 45, Issue 9, pp. 984 - 994
Most psychiatric disorders are moderately to highly heritable. The degree to which genetic variation is unique to individual disorders or shared across... 
ATTENTION-DEFICIT/HYPERACTIVITY DISOR