Genome-wide gene-air pollution interaction analysis of lung function in 300,000 individuals by Melbourne, Carl A., Mesut Erzurumluoglu, A., Shrine, Nick, Chen, Jing, Tobin, Martin D., Hansell, Anna L., Wain, Louise V.

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The Y Chromosome: A Complex Locus for Genetic Analyses of Complex Human Traits by Parker, Katherine, Erzurumluoglu, A Mesut, Rodriguez, Santiago

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Social inequality and the syndemic of chronic disease and COVID-19: county-level analysis in the USA by Islam, Nazrul, Lacey, Ben, Shabnam, Sharmin, Erzurumluoglu, A Mesut, Dambha-Miller, Hajira, Chowell, Gerardo, Kawachi, Ichiro, Marmot, Michael

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COVID-19 and climatic factors: A global analysis by Islam, Nazrul, Bukhari, Qasim, Jameel, Yusuf, Shabnam, Sharmin, Erzurumluoglu, A.Mesut, Siddique, Muhammad A., Massaro, Joseph M., D'Agostino, Ralph B.

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LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation... by Zheng, Jie, Erzurumluoglu, A Mesut, Elsworth, Benjamin L, Kemp, John P, Howe, Laurence, Haycock, Philip C, Hemani, Gibran, Tansey, Katherine, Laurin, Charles, Pourcain, Beate St, Warrington, Nicole M, Finucane, Hilary K, Price, Alkes L, Bulik-Sullivan, Brendan K, Anttila, Verneri, Paternoster, Lavinia, Gaunt, Tom R, Evans, David M, Neale, Benjamin M

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Politics: Listen to accused Turkish scientists by Erzurumluoglu, A Mesut

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Proxy molecular diagnosis from whole-exome sequencing reveals Papillon-Lefevre syndrome caused by a missense mutation in CTSC by Erzurumluoglu, A Mesut, Alsaadi, Muslim M, Rodriguez, Santiago, Alotaibi, Tahani S, Guthrie, Philip A I, Lewis, Sian, Ginwalla, Aasiya, Gaunt, Tom R, Alharbi, Khalid K, Alsaif, Fahad M, Alsaadi, Basma M, Day, Ian N M

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Identifying Highly Penetrant Disease Causal Mutations Using Next Generation Sequencing: Guide to Whole Process by Gaunt, Tom, Richardson, Tom G., Baird, Denis, Shihab, Hashem A., Rodriguez, Santiago, Erzurumluoglu, A. Mesut, Day, Ian N. M.

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Importance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene Functions by Erzurumluoglu, A. Mesut, Shihab, Hashem A., Rodriguez, Santiago, Gaunt, Tom R., Day, Ian N.M.

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Associations of Y chromosomal haplogroups with cardiometabolic risk factors and subclinical vascular measures in males during childhood and adolescence by O'Keeffe, Linda M., Howe, Laura D., Fraser, Abigail, Hughes, Alun D., Wade, Kaitlin H., Anderson, Emma L., Lawlor, Debbie A., Erzurumluoglu, A. Mesut, Davey-Smith, George, Rodriguez, Santiago, Stergiakouli, Evie

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Mitochondrial DNA Haplogroups and Breast Cancer Risk Factors in the Avon Longitudinal Study of Parents and Children (ALSPAC) by Riley, Vivienne, Erzurumluoglu, A Mesut, Rodriguez, Santiago, Bonilla, Carolina

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Y Chromosome, Mitochondrial DNA and Childhood Behavioural Traits by Howe, Laurence J., Erzurumluoglu, A. Mesut, Davey Smith, George, Rodriguez, Santiago, Stergiakouli, Evie

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HAPRAP: a haplotype-based iterative method for statistical fine mapping using GWAS summary statistics by Zheng, Jie, Rodriguez, Santiago, Laurin, Charles, Baird, Denis, Trela-Larsen, Lea, Erzurumluoglu, Mesut A, Zheng, Yi, White, Jon, Giambartolomei, Claudia, Zabaneh, Delilah, Morris, Richard, Kumari, Meena, Casas, Juan P, Hingorani, Aroon D, Evans, David M, Gaunt, Tom R, Day, Ian N M

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Using Y-Chromosomal Haplogroups in Genetic Association Studies and Suggested Implications by Erzurumluoglu, A Mesut, Baird, Denis, Richardson, Tom G, Timpson, Nicholas J, Rodriguez, Santiago

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Listen to accused Turkish scientists by Erzurumluoglu, A. Mesut

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Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci by Liu, Mengzhen, Jackson, Victoria E., Melbourne, Carl A., Young, Robin, Batini, Chiara, Afaq, Saima, Agrawal, Arpana, Antoniou, Antonis C., Baumbach, Clemens, Boehnke, Michael, Brazel, David M, Chen, Chu, Corley, Janie, Chou, Yi-Ling, David, Sean P., de Boer, Rudolf A., Dennis, Joe G., Easton, Douglas F., Eaton, Charles, Goate, Alison, Grabe, Hans J., Haessler, Jeff, Hallmans, Göran, Harris, Sarah E., Hattersley, Andrew, Heath, Andrew, Kapoor, Manav, Karpe, Fredrik, Kooner, Jaspal S., Kooperberg, Charles, Laakso, Markku, Langenberg, Claudia, Luan, Jian’an, Madden, Pamela A. F., Mangino, Massimo, Marouli, Eirini, Marten, Jonathan, McGue, Matt, Moayyeri, Alireza, Moitry, Marie, Naheed, Aliya, Nauck, Matthias, Neville, Matthew J., Nielsen, Sune Fallgaard, Perola, Markus, Pharoah, Paul D. P., Rasheed, Asif, Renström, Frida, Rice, John, Rohde, Rebecca, Samuel, Maria, Scholte, Steven H, Scott, Robert A., Shao, Yaming, Smith, Jennifer A., Starr, John M., Stram, Danielle, Stringham, Heather M., Tachmazidou, Ioanna, Tardif, Jean-Claude, Thompson, Deborah J., Tindle, Hilary A., Tragante, Vinicius, Trompet, Stella, Turcot, Valerie, Tyrrell, Jessica, van der Leij, Andries R, van der Meer, Peter, Verweij, Niek, Warren, Helen R., Weiss, Stefan, Wetherill, Leah, Yaghootkar, Hanieh, Jiang, Yu, Chen, Fang, Zhan, Xiaowei, Zhang, Weihua, Zhao, Wei, Zhao, Wei, Zhou, Kaixin, Amouyel, Philippe, Blankenberg, Stefan, Caulfield, Mark J., Chowdhury, Rajiv, Cucca, Francesco, Deary, Ian J., Deloukas, Panos, Ferrario, Marco, Frossard, Philippe, Hall, Ian P., Jansson, Jan-Håkan, Kee, Frank, Munroe, Patricia B., Palmer, Colin N. A., Sattar, Naveed, Spector, Timothy, Zeggini, Eleftheria, Saleheen, Danish, Danesh, John, Tobin, Martin D.

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Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits by Fetterman, Jessica L., Graff, Mariaelisa, Have, Christian Theil, Yanek, Lisa R., Feitosa, Mary F., Chasman, Daniel I., Young, Kristin, Ligthart, Symen, Hill, W. David, Weiss, Stefan, Luan, Jian’an, Giulianini, Franco, Hartwig, Fernando P., Lin, Shiow J., Wang, Lihua, Fernandez, Eliana P., Ghanbari, Mohsen, Wojczynski, Mary K., Lee, Wen-Jane, Armasu, Sebastian M., Ryan, Kathleen A., An, Ping, Baranski, Thomas J., Bowden, Donald W., Broeckel, Ulrich, Corley, Janie, Rivadeneira, Fernando, Daw, E. Warwick, de las Fuentes, Lisa, Gao, He, Ahluwalia, Tarunveer S., de Mutsert, Renée, Emery, Leslie S., Erzurumluoglu, A. Mesut, Fu, Mao, Gu, Zhenglong, Hunt, Steven C., Jonsson, Anna E., Justice, Anne E., Kerrison, Nicola D., Larson, Nicholas B., Lin, Keng-Hung, Love-Gregory, Latisha D., Mathias, Rasika A., Nauck, Matthias, Ong, Ken K., Pankow, James, Patki, Amit, Qi, Qibin, Schnurr, Theresia M., Sofer, Tamar, Timpson, Nicholas J., de Haan, Hugoline G., Wang, Yujie, Weeke, Peter E., Wu, Hongsheng, Yang, Wei, Zeng, Donglin, Witte, Daniel R., Weir, Bruce S., Vestergaard, Henrik, Torp-Pedersen, Christian, Stergiakouli, Evie, Rosendaal, Frits R., Ikram, M. Arfan, Perls, Thomas T., Pedersen, Oluf, Nohr, Ellen A., Newman, Anne B., Linneberg, Allan, Langenberg, Claudia, Kilpeläinen, Tuomas O., Kardia, Sharon L.R., Jørgensen, Marit E., Jørgensen, Torben, Sørensen, Thorkild I.A., Homuth, Georg, Hansen, Torben, Goodarzi, Mark O., Deary, Ian J., Christensen, Cramer, Chen, Yii-Der Ida, Bonnelykke, Klaus, Wilson, James G., Rodriguez, Santiago, Davies, Gail, Horta, Bernardo L., Thyagarajan, Bharat, Rao, D.C., Grarup, Niels, Davila-Roman, Victor G., Guo, Xiuqing, Tiwari, Hemant K., Loos, Ruth J.F., Dehghan, Abbas, Malik, Afshan N., Becker, Diane M., de Andrade, Mariza, Meigs, James B., Rotter, Jerome I.

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Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use by Jiang, Yu, Hughey, Jordan M., Zhan, Xiaowei, Gong, Jian, Batini, Chiara, Liu, MengZhen, Surendran, Praveen, Young, Robin, Nielsen, Sune Fallgaard, Kontto, Jukka, Perola, Markus, Caslake, Muriel, Reily, Dermot F., Vogt, Thomas, Sattar, Naveed, Ford, Ian, Alam, Dewan S., Majumder, Abdulla al Shafi, Di Angelantonio, Emanuele, Chowdhury, Rajiv, Arveiler, Dominique, Blankenberg, Stefan, Veronesi, Giovanni, EPIC-CVD Consortium, Frossard, Philippe, Nordestgaard, Børge Grønne, Saleheen, Danish, Danesh, John, Butterworth, Adam S., Warren, Helen R., Tragante, Vinicius, Altmaier, Elisabeth, Luan, Jian’an, Scott, Robert A., Stirrups, Kathleen, Marouli, Eirini, Karpe, Fredrik, Poulter, Neil, Rolandsson, Olov, Chambers, John C., Kooner, Jaspal S., Wareham, Nicholas J., Renström, Frida, Hallmans, Göran, Marioni, Riccardo E., Corley, Janie, Starr, John M., van der Meer, Peter, Yavas, Ersin, Vaartjes, Ilonca, Asselbergs, Folkert W., Grabe, Hans J., Nauck, Matthias, Pharoah, Paul D.P., Dunning, Alison M., Dennis, Joe G., Tyrrell, Jessica, Mihailov, Evelin, Metspalu, Andres, Palmer, Colin N.A., Hall, Ian P., Strachan, David P., Understanding Society Scientific Group, Munroe, Patricia B., Jansson, Jan-Håkan, Franks, Paul W., Deloukas, Panos, Chou, Yi-Ling, Faul, Jessica D., Hammerschlag, Anke R., Hsu, Chris, Lai, Dongbing, Le, Nhung, Loukola, Anu, Mangino, Massimo, Melbourne, Carl A., Pistis, Giorgio, Qaiser, Beenish, Stringham, Heather, Wetherill, Leah, Bierut, Laura, Chen, Chu, Eaton, Charles B., Iacono, William G., Polderman, Tinca J., Schlessinger, David, Scholte, H. Steven, Smith, Jennifer A., Boehnke, Michael, Cucca, Francesco, David, Sean P., Foroud, Tatiana, Kardia, Sharon L.R., Madden, Pamela, McGue, Matt, Posthuma, Danielle, Spector, Timothy, Stram, Daniel, Kaprio, Jaakko, Vrieze, Scott

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Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity by Bakker, Mark K., Kanning, Jos P., Abraham, Gad, Martinsen, Amy E., Winsvold, Bendik S., Zwart, John-Anker, Bourcier, Romain, Sawada, Tomonobu, Koido, Masaru, Kamatani, Yoichiro, Morel, Sandrine, Amouyel, Philippe, Debette, Stéphanie, Bijlenga, Philippe, Berrandou, Takiy, Ganesh, Santhi K., Bouatia-Naji, Nabila, Jones, Gregory, Bown, Matthew, Rinkel, Gabriel J.E., Veldink, Jan H., Ruigrok, Ynte M.

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Proxy Molecular Diagnosis from Whole-Exome Sequencing Reveals Papillon-Lefevre Syndrome Caused by a Missense Mutation in CTSC: e0121351 by Erzurumluoglu, A Mesut, Alsaadi, Muslim M, Rodriguez, Santiago, Alotaibi, Tahani S, Guthrie, Philip AI, Lewis, Sian, Ginwalla, Aasiya, Gaunt, Tom R, Alharbi, Khalid K, Alsaif, Fahad M

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