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Number of items: 54.


de Jong, Simone, Abdalla Diniz, Mateus Jose, Saloma, Andiara, Gadelha, Ary, Santoro, Marcos L, Ota, Vanessa K, Noto, Cristiano, Curtis, Charlesg, Newhouse, Stephen J, Patel, Hamel
et al (show 362 more authors) (2018) Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. COMMUNICATIONS BIOLOGY, 1 (1). 163-.


Pulit, Sara L, Weng, Lu-Chen, McArdle, Patrick F, Trinquart, Ludovic, Choi, Seung Hoan, Mitchell, Braxton D, Rosand, Jonathan, de Bakker, Paul IW, Benjamin, Emelia J, Ellinor, Patrick T
et al (show 351 more authors) (2018) Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes. NEUROLOGY-GENETICS, 4 (6). e293-.


Glanville, Kylie P, Coleman, Jonathan RI, Hanscombe, Ken B, Euesden, Jack, Choi, Shing Wan, Purves, Kirstin L, Breen, Gerome, Air, Tracy M, Andlauer, Till FM, Baune, Bernhard T
et al (show 197 more authors) (2020) Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression. BIOLOGICAL PSYCHIATRY, 87 (5). pp. 419-430.


Surendran, Praveen, Feofanova, Elena V, Lahrouchi, Najim, Ntalla, Ioanna, Karthikeyan, Savita, Cook, James, Chen, Lingyan, Mifsud, Borbala, Yao, Chen, Kraja, Aldi T
et al (show 271 more authors) (2020) Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. NATURE GENETICS, 52 (12). pp. 1314-1332.


Karasik, David, Zillikens, M Carola, Hsu, Yi-Hsiang, Aghdassi, Ali, Akesson, Kristina, Amin, Najaf, Barroso, Inês, Bennett, David A, Bertram, Lars, Bochud, Murielle
et al (show 147 more authors) (2019) Disentangling the genetics of lean mass. The American journal of clinical nutrition, 109 (2). pp. 276-287.


Foo, Jerome C, Streit, Fabian, Frank, Josef, Witt, Stephanie H, Treutlein, Jens, Baune, Bernhard T, Moebus, Susanne, Joeckel, Karl-Heinz, Forstner, Andreas J, Noethen, Markus M
et al (show 195 more authors) (2019) Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 180 (1). pp. 35-45.


Polimanti, Renato, Peterson, Roseann E, Ong, Jue-Sheng, MacGregor, Stuart, Edwards, Alexis C, Clarke, Toni-Kim, Frank, Josef, Gerring, Zachary, Gillespie, Nathan A, Lind, Penelope A
et al (show 362 more authors) (2019) Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium. PSYCHOLOGICAL MEDICINE, 49 (7). pp. 1218-1226.


Liu, Dajiang J, Peloso, Gina M, Yu, Haojie, Butterworth, Adam S, Wang, Xiao, Mahajan, Anubha, Saleheen, Danish, Emdin, Connor, Alam, Dewan, Alves, Alexessander Couto
et al (show 217 more authors) (2017) Exome-wide association study of plasma lipids in >300,000 individuals. NATURE GENETICS, 49 (12). 1758-+.


Evangelou, Evangelos, Warren, Helen R, Mosen-Ansorena, David, Mifsu, Borbala, Pazoki, Raha, Gao, He, Ntritsos, Georgios, Dimou, Niki, Cabrer, Claudia P, Karaman, Ibrahim
et al (show 271 more authors) (2018) Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature Genetics, 50 (10). pp. 1412-1425.


Hagenaars, Saskia P, Coleman, Jonathan RI, Choi, Shing Wan, Gaspar, Helena, Adams, Mark J, Howard, David M, Hodgson, Karen, Traylor, Matthew, Air, Tracy M, Andlauer, Till FM
et al (show 38 more authors) (2020) Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 183 (6). pp. 309-330.


Sakornsakolpat, Phuwanat, Prokopenko, Dmitry, Lamontagne, Maxime, Reeve, Nicola F, Guyatt, Anna L, Jackson, Victoria E, Shrine, Nick, Qiao, Dandi, Bartz, Traci M, Kim, Deog Kyeom
et al (show 146 more authors) (2019) Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. NATURE GENETICS, 51 (3). 494-+.


Pairo-Castineira, Erola, Clohisey, Sara, Klaric, Lucija, Bretherick, Andrew D, Rawlik, Konrad, Pasko, Dorota, Walker, Susan, Parkinson, Nick, Fourman, Max Head, Russell, Clark D
et al (show 56 more authors) (2021) Genetic mechanisms of critical illness in COVID-19. NATURE, 591 (7848). 92-+.


Pairo-Castineira, Erola ORCID: 0000-0002-2423-3090, Clohisey, Sara, Klaric, Lucija ORCID: 0000-0003-3105-8929, Bretherick, Andrew ORCID: 0000-0001-9258-3140, Rawlik, Konrad, Parkinson, Nick, Pasko, Dorota, Walker, Susan, Richmond, Anne, Fourman, Max Head
et al (show 50 more authors) (2020) Genetic mechanisms of critical illness in Covid-19. medRxiv.


Amin, Najaf, Allebrandt, Karla V, van der Spek, Ashley, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tonu, van Mill, Josine G, Mbarek, Hamdi
et al (show 64 more authors) (2016) Genetic variants in <i>RBFOX3</i> are associated with sleep latency. EUROPEAN JOURNAL OF HUMAN GENETICS, 24 (10). pp. 1488-1495.


Ligthart, Symen, Vaez, Ahmad, Vosa, Urmo, Stathopoulou, Maria G, de Vries, Paul S, Prins, Bram P, Van der Most, Peter J, Tanaka, Toshiko, Naderi, Elnaz, Rose, Lynda M
et al (show 276 more authors) (2018) Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. AMERICAN JOURNAL OF HUMAN GENETICS, 103 (5). pp. 691-706.


Bolton, Jennifer L, Hayward, Caroline, Direk, Nese, Lewis, John G, Hammond, Geoffrey L, Hill, Lesley A, Anderson, Anna, Huffman, Jennifer, Wilson, James F, Campbell, Harry
et al (show 46 more authors) (2014) Genome wide association identifies common variants at the SERPINA6/SERPINA1 locus influencing plasma cortisol and corticosteroid binding globulin. PLoS Genetics, 10 (7). e1004474-.


Power, Robert A, Tansey, Katherine E, Buttenschon, Henriette Normolle, Cohen-Woods, Sarah, Bigdeli, Tim, Hall, Lynsey S, Kutalik, Zoltn, Lee, S Hong, Ripke, Stephan, Steinberg, Stacy
et al (show 66 more authors) (2017) Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium. BIOLOGICAL PSYCHIATRY, 81 (4). pp. 325-335.


Zeng, Yanni, Navarro, Pau, Shirali, Masoud, Howard, David M, Adams, Mark J, Hall, Lynsey S, Clarke, Toni-Kim, Thomson, Pippa A, Smith, Blair H, Murray, Alison
et al (show 29 more authors) (2017) Genome-wide Regional Heritability Mapping Identifies a Locus Within the <i>TOX2</i> Gene Associated With Major Depressive Disorder. BIOLOGICAL PSYCHIATRY, 82 (5). pp. 312-321.


Wray, Naomi R, Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M, Abdellaoui, Abdel, Adams, Mark J, Agerbo, Esben, Air, Tracy M, Andlauer, Till MF
et al (show 208 more authors) (2018) Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. NATURE GENETICS, 50 (05). pp. 668-681.


Fan, Qiao, Pozarickij, Alfred, Tan, Nicholas YQ, Guo, Xiaobo, Verhoeven, Virginie JM ORCID: 0000-0001-7359-7862, Vitart, Veronique ORCID: 0000-0002-4991-3797, Guggenheim, Jeremy A ORCID: 0000-0001-5164-340X, Miyake, Masahiro, Tideman, J Willem L, Khawaja, Anthony P ORCID: 0000-0001-6802-8585
et al (show 50 more authors) (2020) Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error. Communications biology, 3 (1). 133-.


Arnau-Soler, Aleix, Macdonald-Dunlop, Erin, Adams, Mark J, Clarke, Toni-Kim, MacIntyre, Donald J, Milburn, Keith, Navrady, Lauren, Hayward, Caroline, McIntosh, Andrew M, Thomson, Pippa A
et al (show 195 more authors) (2019) Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland. TRANSLATIONAL PSYCHIATRY, 9 (1). 14-.


Coleman, Jonathan RI, Peyrot, Wouter J, Purves, Kirstin L, Davis, Katrina AS, Rayner, Christopher, Choi, Shing Wan, Hubel, Christopher, Gaspar, Helena A, Kan, Carol, Van der Auwera, Sandra
et al (show 215 more authors) (2020) Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. MOLECULAR PSYCHIATRY, 25 (7). pp. 1430-1446.


Arnau-Soler, Aleix ORCID: 0000-0001-9768-0513, Adams, Mark J ORCID: 0000-0002-3599-6018, Generation Scotland, , Major Depressive Disorder Working Group of the Psychiatric Genom, , Hayward, Caroline and Thomson, Pippa A
(2018) Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. PloS one, 13 (12). e0209160-.


Justice, Anne E, Winkler, Thomas W, Feitosa, Mary F, Graff, Misa, Fisher, Virginia A, Young, Kristin, Barata, Llilda, Deng, Xuan, Czajkowski, Jacek, Hadley, David
et al (show 307 more authors) (2017) Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. NATURE COMMUNICATIONS, 8 (1). 14977-.


Mahajan, Anubha, Go, Min Jin, Zhang, Weihua, Below, Jennifer E, Gaulton, Kyle J, Ferreira, Teresa, Horikoshi, Momoko, Johnson, Andrew D, Ng, Maggie CY, Prokopenko, Inga
et al (show 322 more authors) (2014) Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nature Genetics, 46 (3). pp. 234-244.


Grove, Jakob, Ripke, Stephan, Als, Thomas D, Mattheisen, Manuel, Walters, Raymond K, Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A, Anney, Richard
et al (show 266 more authors) (2019) Identification of common genetic risk variants for autism spectrum disorder. NATURE GENETICS, 51 (3). 431-+.


Wheeler, Eleanor, Leong, Aaron, Liu, Ching-Ti, Hivert, Marie-France, Strawbridge, Rona J, Podmore, Clara, Li, Man, Yao, Jie, Sim, Xueling, Hong, Jaeyoung
et al (show 205 more authors) (2017) Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. PLOS MEDICINE, 14 (9). e1002383-.


Czamara, Darina, Eraslan, Goekcen, Page, Christian M, Lahti, Jari, Lahti-Pulkkinen, Marius, Hamalainen, Esa, Kajantie, Eero, Laivuori, Hannele, Villa, Pia M, Reynolds, Rebecca M
et al (show 219 more authors) (2019) Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. NATURE COMMUNICATIONS, 10 (1). 2548-.


Zillikens, M Carola, Demissie, Serkalem, Hsu, Yi-Hsiang, Yerges-Armstrong, Laura M, Chou, Wen-Chi, Stolk, Lisette, Livshits, Gregory, Broer, Linda, Johnson, Toby, Koller, Daniel L
et al (show 183 more authors) (2017) Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. NATURE COMMUNICATIONS, 8 (1). 80-.


Zillikens, M Carola, Demissie, Serkalem, Hsu, Yi-Hsiang, Yerges-Armstrong, Laura M, Chou, Wen-Chi, Stolk, Lisette, Livshits, Gregory, Broer, Linda, Johnson, Toby, Koller, Daniel L
et al (show 183 more authors) (2017) Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (vol 8, 80, 2017). NATURE COMMUNICATIONS, 8 (1). 1414-.


Sung, Yun J, Winkler, Thomas W, de las Fuentes, Lisa, Bentley, Amy R, Brown, Michael R, Kraja, Aldi T, Schwander, Karen, Ntalla, Ioanna, Guo, Xiuqing, Franceschini, Nora
et al (show 287 more authors) (2018) A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. AMERICAN JOURNAL OF HUMAN GENETICS, 102 (3). pp. 375-400.


Niemi, Mari EK, Karjalainen, Juha, Daly, Mark, Ganna, Andrea, Mehtonen, Juha, Cordioli, Mattia, Kaunisto, Mari, Pigazzini, Sara, Donner, Kati, Kivinen, Katja
et al (show 3481 more authors) (2021) Mapping the human genetic architecture of COVID-19. NATURE, 600 (7889). 472-+.


Jackson, Victoria E ORCID: 0000-0002-9758-9784, Latourelle, Jeanne C, Wain, Louise V ORCID: 0000-0003-4951-1867, Smith, Albert V, Grove, Megan L, Bartz, Traci M, Obeidat, Ma'en ORCID: 0000-0002-5443-2752, Province, Michael A, Gao, Wei, Qaiser, Beenish
et al (show 97 more authors) (2018) Meta-analysis of exome array data identifies six novel genetic loci for lung function. Wellcome Open Research, 3. p. 4.


Jackson, Victoria E ORCID: 0000-0002-9758-9784, Latourelle, Jeanne C, Wain, Louise V ORCID: 0000-0003-4951-1867, Smith, Albert V, Grove, Megan L, Bartz, Traci M, Obeidat, Ma'en ORCID: 0000-0002-5443-2752, Province, Michael A, Gao, Wei, Qaiser, Beenish
et al (show 98 more authors) (2018) Meta-analysis of exome array data identifies six novel genetic loci for lung function. Wellcome open research, 3. 4-.


Ntalla, Ioanna, Weng, Lu-Chen, Cartwright, James H, Hall, Amelia Weber, Sveinbjornsson, Gardar, Tucker, Nathan R, Choi, Seung Hoan, Chaffin, Mark D, Roselli, Carolina, Barnes, Michael R
et al (show 177 more authors) (2020) Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. Nature communications, 11 (1). 2542-.


Bentley, Amy R, Sung, Yun J, Brown, Michael R, Winkler, Thomas W, Kraja, Aldi T, Ntalla, Ioanna, Schwander, Karen, Chasman, Daniel I, Lim, Elise, Deng, Xuan
et al (show 291 more authors) (2019) Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. NATURE GENETICS, 51 (4). 636-+.


Roselli, Carolina, Chaffin, Mark D, Weng, Lu-Chen, Aeschbacher, Stefanie, Ahlberg, Gustav, Albert, Christine M, Almgren, Peter, Alonso, Alvaro, Anderson, Christopher D, Aragam, Krishna G
et al (show 208 more authors) (2018) Multi-ethnic genome-wide association study for atrial fibrillation. Nature Genetics, 50 (9). pp. 1225-1233.


Bonnemaijer, Pieter WM, van Leeuwen, Elisabeth M, Iglesias, Adriana I, Gharahkhani, Puya, Vitart, Veronique, Khawaja, Anthony P, Simcoe, Mark, Hoehn, Rene, Cree, Angela J, Igo, Rob P
et al (show 133 more authors) (2019) Multi-trait genome-wide association study identifies new loci associated with optic disc parameters. COMMUNICATIONS BIOLOGY, 2 (1). 435-.


Kraja, Aldi T, Cook, James P, Warren, Helen R, Surendran, Praveen, Liu, Chunyu, Evangelou, Evangelos, Manning, Alisa K, Grarup, Niels, Drenos, Fotios, Sim, Xueling
et al (show 132 more authors) (2017) New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475000 Individuals. CIRCULATION-CARDIOVASCULAR GENETICS, 10 (5). e001778-.


Shrine, Nick, Guyatt, Anna L, Erzurumluoglu, A Mesut, Jackson, Victoria E, Hobbs, Brian D, Melbourne, Carl A, Batini, Chiara, Fawcett, Katherine A, Song, Kijoung, Sakornsakolpat, Phuwanat
et al (show 99 more authors) (2019) New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. NATURE GENETICS, 51 (3). 481-+.


Wain, Louise V, Vaez, Ahmad, Jansen, Rick, Joehanes, Roby, van der Most, Peter J, Erzurumluoglu, A Mesut, O'Reilly, Paul F, Cabrera, Claudia P, Warren, Helen R, Rose, Lynda M
et al (show 236 more authors) (2017) Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. HYPERTENSION, 70 (3). E4-+.


Stanton, Chloe M, Borooah, Shyamanga, Drake, Camilla, Marsh, Joseph A, Campbell, Susan, Lennon, Alan, Soares, Dinesh C, Vallabh, Neeru A ORCID: 0000-0002-0109-4112, Sahni, Jayashree, Cideciyan, Artur V
et al (show 5 more authors) (2017) Novel pathogenic mutations in <i>C1QTNF5</i> support a dominant negative disease mechanism in late-onset retinal degeneration. SCIENTIFIC REPORTS, 7 (1). 12147-.


Turcot, Valerie, Lu, Yingchang, Highland, Heather M, Schurmann, Claudia, Justice, Anne E, Fine, Rebecca S, Bradfield, Jonathan P, Esko, Tonu, Giri, Ayush, Graff, Mariaelisa
et al (show 401 more authors) (2018) Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. NATURE GENETICS, 50 (1). pp. 26-41.


Justice, Anne E, Karaderi, Tugce, Highland, Heather M, Young, Kristin L, Graff, Mariaelisa, Lu, Yingchang, Turcot, Valérie, Auer, Paul L, Fine, Rebecca S, Guo, Xiuqing
et al (show 279 more authors) (2019) Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Nature genetics, 51 (3). 452-+.


Marouli, Eirini, Graff, Mariaelisa, Medina-Gomez, Carolina, Lo, Ken Sin, Wood, Andrew R, Kjaer, Troels R, Fine, Rebecca S, Lu, Yingchang, Schurmann, Claudia, Highland, Heather M
et al (show 363 more authors) (2017) Rare and low-frequency coding variants alter human adult height. NATURE, 542 (7640). pp. 186-190.


Mahajan, Anubha, Wessel, Jennifer, Willems, Sara M, Zhao, Wei, Robertson, Neil R, Chu, Audrey Y, Gan, Wei, Kitajima, Hidetoshi, Taliun, Daniel, Rayner, N William
et al (show 233 more authors) (2018) Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. NATURE GENETICS, 50 (4). 559-571+.


Munn-Chernoff, Melissa A, Johnson, Emma C, Chou, Yi-Ling, Coleman, Jonathan RI, Thornton, Laura M, Walters, Raymond K, Yilmaz, Zeynep, Baker, Jessica H, Hubel, Christopher, Gordon, Scott
et al (show 342 more authors) (2021) Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. ADDICTION BIOLOGY, 26 (1). e12880-.


Surendran, Praveen, Drenos, Fotios, Young, Robin, Warren, Helen, Cook, James P, Manning, Alisa K, Grarup, Niels, Sim, Xueling, Barnes, Daniel R, Witkowska, Kate
et al (show 200 more authors) (2016) Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. NATURE GENETICS, 48 (10). pp. 1151-1161.


Giri, Ayush, Hellwege, Jacklyn N, Keaton, Jacob M, Park, Jihwan, Qiu, Chengxiang, Warren, Helen R, Torstenson, Eric S, Kovesdy, Csaba P, Sun, Yan V, Wilson, Otis D
et al (show 88 more authors) (2019) Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. NATURE GENETICS, 51 (1). 51-+.


Walters, Raymond K, Polimanti, Renato, Johnson, Emma C, McClintick, Jeanette N, Adams, Mark J, Adkins, Amy E, Aliev, Fazil, Bacanu, Silviu-Alin, Batzler, Anthony, Bertelsen, Sarah
et al (show 158 more authors) (2018) Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nature Neuroscience, 21 (12). pp. 1656-1669.


Crawford, Andrew A, Bankier, Sean, Altmaier, Elisabeth, Barnes, Catriona LK, Clark, David W, Ermel, Raili, Friedrich, Nele, van der Harst, Pim, Joshi, Peter K, Karhunen, Ville
et al (show 30 more authors) (2021) Variation in the <i>SERPINA6/SERPINA1</i> locus alters morning plasma cortisol, hepatic corticosteroid binding globulin expression, gene expression in peripheral tissues, and risk of cardiovascular disease. JOURNAL OF HUMAN GENETICS, 66 (6). pp. 625-636.


Wuttke, Matthias, Li, Yong, Li, Man, Sieber, Karsten B, Feitosa, Mary F, Gorski, Mathias, Tin, Adrienne, Wang, Lihua, Chu, Audrey Y, Hoppmann, Anselm
et al (show 318 more authors) (2019) A catalog of genetic loci associated with kidney function from analyses of a million individuals. NATURE GENETICS, 51 (6). 957-+.


Rahmioglu, Nilufer, Mortlock, Sally, Ghiasi, Marzieh, Moller, Peter L, Stefansdottir, Lilja, Galarneau, Genevieve, Turman, Constance, Danning, Rebecca, Law, Matthew H, Sapkota, Yadav
et al (show 123 more authors) (2023) The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. NATURE GENETICS, 55 (3). 423-+.


Ried, Janina S, Jeff, Janina M, Chu, Audrey Y, Bragg-Gresham, Jennifer L, van Dongen, Jenny, Huffman, Jennifer E, Ahluwalia, Tarunveer S, Cadby, Gemma, Eklund, Niina, Eriksson, Joel
et al (show 266 more authors) (2016) A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. NATURE COMMUNICATIONS, 7 (1). 13357-.

This list was generated on Sun Mar 10 06:39:34 2024 GMT.