The magnetic ordering in high magnetoresistance Mn-doped ZnO thin films

by Venkatesh, S., Baras, A., Lee, J.-S., Roqan, I. S.
Published in AIP advances

Translating polygenic risk scores for clinical use by estimating the confidence bounds of risk prediction

by Sun, Jiangming, Wang, Yunpeng, Folkersen, Lasse, Borné, Yan, Amlien, Inge, Buil, Alfonso, Orho-Melander, Marju, Børglum, Anders D, Hougaard, David M, Melander, Olle, Engström, Gunnar, Werge, Thomas, Lage, Kasper
Published in Nature communications

Residual muscle-invasive disease at cystectomy is not accurately predicted by post-chemotherapy restaging protocols including DNA damage response gene mutation analysis

by Becker, R.E.N., Baras, A., Meyer, A.R., Brant, A., Reese, A.C., Netto, G.J., Matoso, A., Hoffman-Censits, J.H., Hahn, N.M., Choi, W., McConkey, D.J., Pierorazio, P.M., Johnson, M.H., Schoenberg, M.P., Kates, M.R., Bivalacqua, T.J.
Published in European urology open science (Online)

A case of a non-immunocompromised adult with fever, mononucleosis and a serological puzzle

by Alidjinou, E.K, Baras, A, Lambert, M, Dewilde, A, Hober, D
Published in Journal of clinical virology

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

by Shah, Sonia, Roselli, Carolina, Lin, Honghuang, Fatemifar, Ghazaleh, Hedman, Åsa K, Morley, Michael P, Verweij, Niek, Dehghan, Abbas, Almgren, Peter, Ärnlöv, Johan, Backman, Joshua D, Biggs, Mary L, Bloom, Heather L, Brown, Michael R, Buckbinder, Leonard, Chasman, Daniel I, Chen, Xing, Chen, Xu, Chung, Jonathan, Chutkow, William, Delgado, Graciela E, Denaxas, Spiros, Dörr, Marcus, Dudley, Samuel C, Dunn, Michael E, Felix, Stephan B, Finan, Chris, Ghanbari, Mohsen, Ghasemi, Sahar, Giedraitis, Vilmantas, Giulianini, Franco, Gottdiener, John S, Gross, Stefan, Guðbjartsson, Daníel F, van der Harst, Pim, Hyde, Craig L, Ingelsson, Erik, Jukema, J Wouter, Khaw, Kay-Tee, Kleber, Marcus E, Køber, Lars, Koekemoer, Andrea, Langenberg, Claudia, Lind, Lars, London, Barry, Lovering, Ruth C, Luan, Jian'an, Magnusson, Patrik, Mahajan, Anubha, Melander, Olle, Mordi, Ify R, Morgan, Thomas, Morris, Andrew D, Morris, Andrew P, Morrison, Alanna C, Nagle, Michael W, Niessner, Alexander, O'Donoghue, Michelle L, Owens, Anjali T, Palmer, Colin N A, Parry, Helen M, Portilla-Fernandez, Eliana, Psaty, Bruce M, Rice, Kenneth M, Ridker, Paul M, Romaine, Simon P R, Salo, Perttu, Salomaa, Veikko, Smith, Nicholas L, Stender, Steen, Stott, David J, Svensson, Per, Taylor, Kent D, Teumer, Alexander, Thorgeirsson, Guðmundur, Thorsteinsdottir, Unnur, Tyl, Benoit, Uitterlinden, Andre G, Veluchamy, Abirami, Völker, Uwe, Voors, Adriaan A, Wang, Xiaosong, Waterworth, Dawn, Weiss, Raul, Wiggins, Kerri L, Xing, Heming, Yerges-Armstrong, Laura M, Yu, Bing, Zannad, Faiez, Zhao, Jing Hua, Hemingway, Harry, Samani, Nilesh J, Malarstig, Anders, Asselbergs, Folkert W, Kuchenbaecker, Karoline, Lang, Chim C, Stefansson, Kari, Smith, J Gustav, Swerdlow, Daniel I, Lumbers, R Thomas
Published in Nature communications

Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations

by Boer, Cindy G., Hatzikotoulas, Konstantinos, Southam, Lorraine, Zhang, Yanfei, Coutinho de Almeida, Rodrigo, Wu, Tian T., Zheng, Jie, Hartley, April, Teder-Laving, Maris, Terao, Chikashi, Zengini, Eleni, Alexiadis, George, Bjornsdottir, Gyda, Gilly, Arthur, Ingvarsson, Thorvaldur, Luetge, Almut, Lund, Sigrun H., Mangino, Massimo, Takuwa, Hiroshi, Thomas, Laurent F., Loughlin, John, Arden, Nigel, Doherty, Michael, Ollier, William E.R., Spector, Tim D., Wallis, Gillian A., Martinsen, Amy E., Fors, Egil Andreas, Hagen, Knut, Nilsen, Kristian Bernhard, Lie, Marie Udnesseter, Børte, Sigrid, Brumpton, Ben, Fritsche, Lars G., Zhou, Wei, Heuch, Ingrid, Storheim, Kjersti, Tyrpenou, Evangelos, Koukakis, Athanasios, Efstathios, Chronopoulos, Nikolaou, Vasileios S., Malizos, Konstantinos, Anastasopoulou, Lydia, Abecasis, Goncalo, Baras, Aris, Cantor, Michael, Coppola, Giovanni, Lotta, Luca A., Shuldiner, Alan, Karalis, Katia, Siminovitch, Katherine, Beechert, Christina, Forsythe, Caitlin, Fuller, Erin D., Gu, Zhenhua, Lattari, Michael, Padilla, Maria Sotiropoulos, Widom, Louis, Wolf, Sarah E., Pradhan, Manasi, Manoochehri, Kia, Bai, Xiaodong, Balasubramanian, Suganthi, Boutkov, Boris, Eom, Gisu, Habegger, Lukas, Hawes, Alicia, Maxwell, Evan K., Orelus, Max, Panea, Razvan, Polanco, Tommy, Salerno, William, Staples, Jeffrey C., Li, Dadong, Sharma, Deepika, Banerjee, Ilanjana, Locke, Adam, Haas, Mary, Akbari, Parsa, Ferreira, Manuel A.R., Jones, Marcus B., Mitnaul, Lyndon J., Babis, George C., Cheung, Jason Pui Yin, Kang, Jae Hee, Lietman, Steven A., Samartzis, Dino, Stefansson, Kari, Uitterlinden, André G., Davey Smith, George, Valdes, Ana M., Tsezou, Aspasia, Cheah, Kathryn S.E., Hveem, Kristian, Wilkinson, J. Mark, Meulenbelt, Ingrid, Lee, Ming Ta Michael, van Meurs, Joyce B.J., Styrkársdóttir, Unnur, Zeggini, Eleftheria
Published in Cell

Potentiation of the anticancer effect of valproic acid, an antiepileptic agent with histone deacetylase inhibitory activity, by the kinase inhibitor Staurosporine or its clinically...

by YEOW, W.-S, ZIAUDDIN, M. F, MAXHIMER, J. B, SHAMIMI-NOORI, S, BARAS, A, CHUA, A, SCHRUMP, D. S, NGUYEN, D. M
Published in British journal of cancer

Severe Acute Respiratory Syndrome Coronavirus 2 Infection Among Healthcare Workers in South Africa: A Longitudinal Cohort Study

by Nunes, Marta C, Baillie, Vicky L, Kwatra, Gaurav, Bhikha, Sutika, Verwey, Charl, Menezes, Colin, Cutland, Clare L, Moore, David P, Dangor, Ziyaad, Adam, Yasmin, Mathivha, Rudo, Velaphi, Sithembiso C, Tsitsi, Merika, Aguas, Ricardo, Madhi, Shabir A
Published in Clinical infectious diseases

ALG9 Mutation Carriers Develop Kidney and Liver Cysts

by Besse, Whitney, Chang, Alex R, Luo, Jonathan Z, Triffo, William J, Moore, Bryn S, Gulati, Ashima, Hartzel, Dustin N, Mane, Shrikant, Torres, Vicente E, Somlo, Stefan, Mirshahi, Tooraj
Published in Journal of the American Society of Nephrology

Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

by Li, Yong, Wuttke, Matthias, Winkler, Thomas W., Chai, Jin-Fang, Chu, Audrey Y., Cocca, Massimiliano, Feitosa, Mary F., Hoppmann, Anselm, Horn, Katrin, Li, Man, Nutile, Teresa, Tin, Adrienne, Tayo, Bamidele O., Bakker, Stephan J.L., Banas, Bernhard, Biggs, Mary L., Bottinger, Erwin P., Brenner, Hermann, Chalmers, John, Chee, Miao-Ling, Degenhardt, Frauke, Eckardt, Kai-Uwe, Ghanbari, Mohsen, Gieger, Christian, Hofer, Edith, Xian Foo, Valencia Hui, Hutri-Kähönen, Nina, Ikram, M. Arfan, Kähönen, Mika, Khor, Chiea-Chuen, Koenig, Wolfgang, Kramer, Holly, Krämer, Bernhard K., Kühnel, Brigitte, Lange, Leslie A., Franke, Lude, van der Harst, Pim, Navis, Gerjan, Snieder, Harold, Swertz, Morris, Wolffenbuttel, Bruce H.R., Wijmenga, Cisca, Abecasis, Goncalo, Baras, Aris, Coppola, Giovanni, Economides, Aris, Lotta, Luca A., Overton, John D., Reid, Jeffrey G., Beechert, Christina, Forsythe, Caitlin, Gu, Zhenhua, Lattari, Michael, Padilla, Maria Sotiropoulos, Toledo, Karina, Pradhan, Manasi, Manoochehri, Kia, Ulloa, Ricardo H., Bai, Xiaodong, Barnard, Leland, Blumenfeld, Andrew, Habegger, Lukas, Hawes, Alicia, Khalid, Shareef, Maxwell, Evan K., Salerno, William, Mitnaul, Lyndon J., Loos, Ruth J.F., Meisinger, Christa, Meitinger, Thomas, Melander, Olle, Milaneschi, Yuri, Mishra, Pashupati P., Mychaleckyj, Josyf C., Nikus, Kjell, Nolte, Ilja M., O’Donoghue, Michelle L., Pendergrass, Sarah A., Penninx, Brenda W.J.H., Preuss, Michael H., Psaty, Bruce M., Raitakari, Olli T., Rettig, Rainer, Rheinberger, Myriam, Rice, Kenneth M., Rosenkranz, Alexander R., Rossing, Peter, Sedaghat, Sanaz, Taylor, Kent D., Tremblay, Johanne, Völker, Uwe, Wallentin, Lars, Waterworth, Dawn M., White, Harvey D., Wilson, James G., Wong, Tien-Yin, Snieder, Harold, Böger, Carsten A., Köttgen, Anna, Heid, Iris M.
Published in Kidney international

Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals

by Kember, Rachel L., Merikangas, Alison K., Verma, Shefali S., Verma, Anurag, Judy, Renae, Abecasis, Goncalo, Baras, Aris, Cantor, Michael, Coppola, Giovanni, Economides, Aris, Lotta, Luca, Overton, John D., Reid, Jeffrey G., Shuldiner, Alan, Beechert, Christina, Forsythe, Caitlin, Fuller, Erin D., Gu, Zhenhua, Lattari, Michael, Lopez, Alexander, Schleicher, Thomas D., Padilla, Maria Sotiropoulos, Toledo, Karina, Widom, Louis, Wolf, Sarah E., Pradhan, Manasi, Manoochehri, Kia, Ulloa, Ricardo H., Bai, Xiaodong, Balasubramanian, Suganthi, Barnard, Leland, Blumenfeld, Andrew, Eom, Gisu, Habegger, Lukas, Hahn, Young, Hawes, Alicia, Khalid, Shareef, Maxwell, Evan K., Salerno, William, Staples, Jeffrey C., Yadav, Ashish, Jones, Marcus B., Mitnaul, Lyndon J., Damrauer, Scott M., Ritchie, Marylyn D., Rader, Daniel J., Bućan, Maja
Published in Biological psychiatry (1969)

GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms

by Ward, Lucas D, Tu, Ho-Chou, Quenneville, Chelsea B, Tsour, Shira, Flynn-Carroll, Alexander O, Parker, Margaret M, Deaton, Aimee M, Haslett, Patrick A J, Lotta, Luca A, Verweij, Niek, Ferreira, Manuel A R, Baras, Aris, Hinkle, Gregory, Nioi, Paul
Published in Nature communications

Heterozygosity for a Pathogenic Variant in SLC12A3 That Causes Autosomal Recessive Gitelman Syndrome Is Associated with Lower Serum Potassium

by Wan, Xuesi, Perry, James, Zhang, Haichen, Jin, Feng, Ryan, Kathleen A, Van Hout, Cristopher, Reid, Jeffrey, Overton, John, Baras, Aris, Han, Zhe, Streeten, Elizabeth, Li, Yanbing, Mitchell, Braxton D, Shuldiner, Alan R, Fu, Mao
Published in Journal of the American Society of Nephrology

Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes

by Deaton, Aimee M, Parker, Margaret M, Ward, Lucas D, Flynn-Carroll, Alexander O, BonDurant, Lucas, Hinkle, Gregory, Akbari, Parsa, Lotta, Luca A, Baras, Aris, Nioi, Paul
Published in Scientific reports

Genetic Susceptibility to Mood Disorders and Risk of Stroke: A Polygenic Risk Score and Mendelian Randomization Study

by Sun, Jiangming, Borné, Yan, Edsfeldt, Andreas, Wang, Yunpeng, Pan, Mengyu, Melander, Olle, Engström, Gunnar, Gonçalves, Isabel
Published in Stroke (1970)

Classic Thrombophilias and Thrombotic Risk Among Middle-Aged and Older Adults: A Population-Based Cohort Study

by Manderstedt, Eric, Lind-Halldén, Christina, Halldén, Christer, Elf, Johan, Svensson, Peter J, Dahlbäck, Björn, Engström, Gunnar, Melander, Olle, Baras, Aris, Lotta, Luca A, Zöller, Bengt
Published in Journal of the American Heart Association

Performance of polygenic risk scores for cancer prediction in a racially diverse academic biobank

by Wang, Louise, Desai, Heena, Verma, Shefali S., Le, Anh, Hausler, Ryan, Verma, Anurag, Judy, Renae, Doucette, Abigail, Gabriel, Peter E., Abecasis, Goncalo, Bai, Xiaodong, Balasubramanian, Suganthi, Baras, Aris, Blumenfeld, Andrew, Boutkov, Boris, Cantor, Michael, Coppola, Giovanni, Economides, Aris, Eom, Gisu, Habegger, Lukas, Hawes, Alicia, Jones, Marcus B., Khalid, Shareef, Krasheninina, Olga, Lanche, Rouel, Lotta, Luca A., Mansfield, Adam J., Maxwell, Evan K., Mighty, Jason, Mitnaul, Lyndon J., Nafde, Mrunali, O’Keeffe, Sean, Orelus, Max, Overton, John D., Panea, Razvan, Polanco, Tommy, Rasool, Ayesha, Reid, Jeffrey G., Salerno, William, Staples, Jeffrey C., Shuldiner, Alan, Beechert, Christina, Forsythe, Caitlin, Fuller, Erin D., Gu, Zhenhua, Lattari, Michael, Lopez, Alexander, Manoochehri, Kia, Pradhan, Manasi, Schleicher, Thomas D., Padilla, Maria Sotiropoulos, Ulloa, Ricardo H., Widom, Louis, Wolf, Sarah E., Nathanson, Katherine L., Damrauer, Scott M., Mowery, Danielle L., Ritchie, Marylyn D., Kember, Rachel L., Maxwell, Kara N.
Published in Genetics in medicine

Home-based digital leisure: Doing the same leisure activities, but digital

by López-Sintas, Jordi, Rojas-DeFrancisco, Laura, García-Álvarez, Ercilia
Published in Cogent social sciences

Cell cycle biomarker discovery for phase 0 clinical trials in type II endometrial cancer

by Stone, R.L., Beavis, A.L., Baras, A., Wang, T.L., Yen, T.T., Chui, M.H., Lin, S.F., Bahadirli-Talbott, A., Temkin, S.M.
Published in Gynecologic oncology

Assessment of genetic susceptibility to multiple primary cancers through whole-exome sequencing in two large multi-ancestry studies

by Cavazos, Taylor B, Kachuri, Linda, Graff, Rebecca E, Nierenberg, Jovia L, Thai, Khanh K, Alexeeff, Stacey, Van Den Eeden, Stephen, Corley, Douglas A, Kushi, Lawrence H, Hoffmann, Thomas J, Ziv, Elad, Habel, Laurel A, Jorgenson, Eric, Sakoda, Lori C, Witte, John S
Published in BMC medicine