Contribution of rare whole-genome sequencing variants to plasma protein levels and the missing heritability by Kierczak, Marcin, Rafati, Nima, Höglund, Julia, Gourlé, Hadrien, Lo Faro, Valeria, Schmitz, Daniel, Ek, Weronica E., Gyllensten, Ulf, Enroth, Stefan, Ekman, Diana, Nystedt, Björn, Karlsson, Torgny, Johansson, Åsa

Get full text

Copy number variations and their effect on the plasma proteome by Schmitz, Daniel, Li, Zhiwei, Lo Faro, Valeria, Rask-Andersen, Mathias, Ameur, Adam, Rafati, Nima, Johansson, Åsa

Get full text

Genome-wide CNV investigation suggests a role for cadherin, Wnt, and p53 pathways in primary open-angle glaucoma by Lo Faro, Valeria, ten Brink, Jacoline B, Snieder, Harold, Jansonius, Nomdo M, Bergen, Arthur A

Get full text

Multi-ancestry polygenic risk scores for venous thromboembolism by Jee, Yon Ho, Thibord, Florian, Dominguez, Alicia, Sept, Corriene, Boulier, Kristin, Venkateswaran, Vidhya, Ding, Yi, Cherlin, Tess, Verma, Shefali Setia, Faro, Valeria Lo, Bartz, Traci M, Boland, Anne, Brody, Jennifer A, Deleuze, Jean-Francois, Emmerich, Joseph, Germain, Marine, Johnson, Andrew D, Kooperberg, Charles, Morange, Pierre-Emmanuel, Pankratz, Nathan, Psaty, Bruce M, Reiner, Alexander P, Smadja, David M, Sitlani, Colleen M, Suchon, Pierre, Tang, Weihong, Trégouët, David-Alexandre, Zöllner, Sebastian, Pasaniuc, Bogdan, Damrauer, Scott M, Sanna, Serena, Snieder, Harold, Kabrhel, Christopher, Smith, Nicholas L, Kraft, Peter

Get full text

Mitochondrial Genome Study Identifies Association Between Primary Open-Angle Glaucoma and Variants in MT-CYB, MT-ND4 Genes and Haplogroups by Lo Faro, Valeria, Nolte, Ilja M, Ten Brink, Jacoline B, Snieder, Harold, Jansonius, Nomdo M, Bergen, Arthur A

Get full text

Differences in clinical presentation of primary open‐angle glaucoma between African and European populations by Bonnemaijer, Pieter W. M., Lo Faro, Valeria, Sanyiwa, Anna J., Hassan, Hassan G., Cook, Colin, Van de Laar, Suzanne, Lemij, Hans G., Klaver, Caroline C. W., Jansonius, Nomdo M., Thiadens, Alberta A. H. J.

Get full text

Influence of electromagnetic radiation emitted by daily-use electronic devices on the Eyemate® system in-vitro: a feasibility study by Invernizzi, Azzurra, Haykal, Shereif, Lo Faro, Valeria, Pennisi, Vincenzo, Choritz, Lars

Get full text

A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus by Hardcastle, Alison J., Liskova, Petra, Bykhovskaya, Yelena, McComish, Bennet J., Davidson, Alice E., Inglehearn, Chris F., Li, Xiaohui, Choquet, Hélène, Habeeb, Mahmoud, Lucas, Sionne E. M., Sahebjada, Srujana, Pontikos, Nikolas, Lopez, Karla E. Rojas, Khawaja, Anthony P., Ali, Manir, Dudakova, Lubica, Skalicka, Pavlina, Van Dooren, Bart T. H., Geerards, Annette J. M., Haudum, Christoph W., Faro, Valeria Lo, Tenen, Abi, Simcoe, Mark J., Patasova, Karina, Yarrand, Darioush, Yin, Jie, Siddiqui, Salina, Rice, Aine, Farraj, Layal Abi, Chen, Yii-Der Ida, Rahi, Jugnoo S., Krauss, Ronald M., Theusch, Elisabeth, Charlesworth, Jac C., Szczotka-Flynn, Loretta, Toomes, Carmel, Meester-Smoor, Magda A., Richardson, Andrea J., Mitchell, Paul A., Taylor, Kent D., Melles, Ronald B., Aldave, Anthony J., Mills, Richard A., Cao, Ke, Chan, Elsie, Daniell, Mark D., Wang, Jie Jin, Rotter, Jerome I., Hewitt, Alex W., MacGregor, Stuart, Klaver, Caroline C. W., Ramdas, Wishal D., Craig, Jamie E., Iyengar, Sudha K., O’Brart, David, Jorgenson, Eric, Baird, Paul N., Rabinowitz, Yaron S., Burdon, Kathryn P., Hammond, Chris J., Tuft, Stephen J., Hysi, Pirro G.

Get full text

Genotyping oral contraceptive users for venous thromboembolism risk by Lo Faro, Valeria, Johansson, Åsa

Get full text

The risk of venous thromboembolism in oral contraceptive users: the role of genetic factors—a prospective cohort study of 240,000 women in the UK Biobank by Lo Faro, Valeria, Johansson, Therese, Johansson, Åsa

Get full text

Answer to the Hamlet-like dilemma of lipid metabolites causing senile macular degeneration by Lo Faro, Valeria

Get full text

Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld‐Rieger syndrome by Lo Faro, Valeria, Siddiqui, Sorath N., Khan, Muhammad I., Villanueva‐Mendoza, Cristina, Cortés‐González, Vianney, Jansonius, Nomdo, Bergen, Arthur A. B., Micheal, Shazia

Get full text

Polygenic risk scores and risk stratification in deep vein thrombosis by Lo Faro, Valeria, Johansson, Therese, Höglund, Julia, Hadizadeh, Fatemeh, Johansson, Åsa

Get full text

Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease by Zhou, Wei, Tsuo, Kristin, Hirbo, Jibril B., Wang, Ying, Bhattacharya, Arjun, Zhao, Huiling, Surakka, Ida, Wolford, Brooke N., Lo Faro, Valeria, Lopera-Maya, Esteban A., Läll, Kristi, Favé, Marie-Julie, Chapman, Sinéad B., Karjalainen, Juha, Maasha, Mutaamba, Chavan, Sameer, Daya, Michelle, Ding, Yi, Feng, Yen-Chen A., Guare, Lindsay A., Gignoux, Christopher R., Graham, Sarah E., Ingold, Nathan, Ismail, Said I., Laisk, Triin, Lin, Kuang, Millwood, Iona Y., Moreno-Grau, Sonia, Nam, Kisung, Palta, Priit, Saad, Chadi, Setia-Verma, Shefali, Thorsteinsdottir, Unnur, Verma, Anurag, Zawistowski, Matthew, Afifi, Nahla, Al-Dabhani, Kawthar M., Campbell, Archie, Crooks, Kristy, Fritsche, Lars G., Fthenou, Eleni, Guo, Yu, Hunt, Karen A., Ioannidis, Alexander, Jansonius, Nomdo M., Konuma, Takahiro, Lee, Ming Ta Michael, Lopez-Pineda, Arturo, Matsuda, Yuta, Marioni, Riccardo E., Numakura, Kensuke, Patil, Snehal, Richmond, Anne, Rojas-Muñoz, Agustin, Shortt, Jonathan A., Tao, Ran, Vanderwerff, Brett, Vernekar, Manvi, Veturi, Yogasudha, Barnes, Kathleen C., Chen, Zhengming, Smith, George Davey, Finucane, Hilary K., Gamazon, Eric R., Gaunt, Tom R., Ge, Tian, Katsanis, Nicholas, Koskela, Jukka T., Law, Matthew H., Li, Liming, Loos, Ruth J.F., Matsuda, Koichi, Olsen, Catherine M., Shavit, Jordan A., Snieder, Harold, Takano, Tomohiro, Vonk, Judith M., Wicks, Stephen J., Wijmenga, Cisca, Wright, John, Zhou, Xiang, Awadalla, Philip, Boehnke, Michael, Bustamante, Carlos D., Fatumo, Segun, Hayward, Caroline, Hveem, Kristian, Kenny, Eimear E., Lee, Seunggeun, Mbarek, Hamdi, Mägi, Reedik, Martin, Hilary C., Medland, Sarah E., Palotie, Aarno V., Pasaniuc, Bogdan, Rader, Daniel J., Ritchie, Marylyn D., Smoller, Jordan W., Stefansson, Kari, Martin, Alicia R.

Get full text

Familial 18q12.2 deletion supports the role of RNA‐binding protein CELF4 in autism spectrum disorders by Barone, Rita, Fichera, Marco, De Grandi, Mariaclara, Battaglia, Marta, Lo Faro, Valeria, Mattina, Teresa, Rizzo, Renata

Get full text

Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts by Wang, Ying, Namba, Shinichi, Lopera, Esteban, Kerminen, Sini, Kanai, Masahiro, Zhou, Wei, Bhatta, Laxmi, Awadalla, Philip, Hveem, Kristian, Lo Faro, Valeria, Mägi, Reedik, Sanna, Serena, Smoller, Jordan W., Uzunovic, Jasmina, Zhou, Wei, Kanai, Masahiro, Rasheed, Humaira, Tsuo, Kristin, Hirbo, Jibril B., Bhattacharya, Arjun, Zhao, Huiling, Namba, Shinichi, Surakka, Ida, Wolford, Brooke N., Lo Faro, Valeria, Läll, Kristi, Favé, Marie-Julie, Chapman, Sinéad B., Karjalainen, Juha, Kurki, Mitja, Mutaamba, Maasha, Partanen, Juulia J., Chavan, Sameer, Chen, Tzu-Ting, Daya, Michelle, Ding, Yi, Graham, Sarah E., Ingold, Nathan, Johnson, Ruth, Laisk, Triin, Lin, Kuang, Lv, Jun, Millwood, Iona Y., Pandit, Anita, Preuss, Michael H., Thorsteinsdottir, Unnur, Uzunovic, Jasmina, Zawistowski, Matthew, Zhong, Xue, Campbell, Archie, Douville, Nicholas J., Finer, Sarah, Griffiths, Christopher J., Marioni, Riccardo E., Nomdo, Jansonius, Patil, Snehal, Richmond, Anne, Straub, Peter, Vanderwerff, Brett, Barnes, Kathleen C., Chen, Zhengming, Chen, Chia-Yen, Smith, George Davey, Finucane, Hilary K., Franke, Lude, Gamazon, Eric R., Ganna, Andrea, Gaunt, Tom R., Ge, Tian, Huffman, Jennifer, MacGregor, Stuart, Matsuda, Koichi, Olsen, Catherine M., Porteous, David J., Shavit, Jordan A., Trembath, Richard C., Vonk, Judith M., Whiteman, David, Wicks, Stephen J., Wijmenga, Cisca, Wright, John, Zhou, Xiang, Cox, Nancy J., Geschwind, Daniel H., Hayward, Caroline, Hveem, Kristian, Kenny, Eimear E., Lin, Yen-Feng, Mägi, Reedik, Martin, Hilary C., Walters, Robin G., Zöllner, Sebastian, Martin, Alicia R., Willer, Cristen J., Daly, Mark J., Neale, Benjamin M., Surakka, Ida, Okada, Yukinori, Martin, Alicia R., Hirbo, Jibril

Get full text

Meta-analysis fine-mapping is often miscalibrated at single-variant resolution by Zhou, Wei, Zhou, Wei, Wu, Kuan-Han H., Hirbo, Jibril B., Lopera-Maya, Esteban A., Läll, Kristi, Karjalainen, Juha, Kurki, Mitja, Maasha, Mutaamba, Brumpton, Ben M., Chavan, Sameer, Chen, Tzu-Ting, Ding, Yi, Guare, Lindsay A., Hornsby, Whitney E., Ingold, Nathan, Johnson, Ruth, Laisk, Triin, Lv, Jun, Millwood, Iona Y., Palta, Priit, Uzunovic, Jasmina, Verma, Anurag, Zawistowski, Matthew, Zhong, Xue, Al-Dabhani, Kawthar M., Campbell, Archie, Damrauer, Scott M., Douville, Nicholas J., Finer, Sarah, Fritsche, Lars G., Fthenou, Eleni, Gonzalez-Arroyo, Gilberto, Hunt, Karen A., Ioannidis, Alexander, Jansonius, Nomdo M., Michael Lee, Ming Ta, Lopez-Pineda, Arturo, Marioni, Riccardo E., Moatamed, Babak, Numakura, Kensuke, Rafaels, Nicholas, Richmond, Anne, Rojas-Muñoz, Agustin, Straub, Peter, Vanderwerff, Brett, Vernekar, Manvi, Barnes, Kathleen C., Boezen, Marike, Chen, Zhengming, Chen, Chia-Yen, Cho, Judy, Finucane, Hilary K., Franke, Lude, Ganna, Andrea, Gaunt, Tom R., Huang, Hailiang, Koskela, Jukka T., Lajonchere, Clara, Loos, Ruth J.F., MacGregor, Stuart, Matsuda, Koichi, Olsen, Catherine M., Porteous, David J., Shavit, Jordan A., Takano, Tomohiro, Vonk, Judith M., Whiteman, David C., Wright, John, Boehnke, Michael, Bustamante, Carlos D., Cox, Nancy J., Fatumo, Segun, Geschwind, Daniel H., Hayward, Caroline, Mägi, Reedik, Martin, Hilary C., Medland, Sarah E., Okada, Yukinori, Palotie, Aarno V., Pasaniuc, Bogdan, Sanna, Serena, Stefansson, Kari, Zöllner, Sebastian, BioMe, BioVU, CanPath - Ontario Health Study, China Kadoorie Biobank Collaborative Group, Colorado Center for Personalized Medicine, deCODE Genetics, Estonian Biobank, FinnGen, Generation Scotland, National Biobank of Korea, Taiwan Biobank, The Hunt Study, Ucla Atlas Community Health Initiative, Uganda Genome Resource, Uk Biobank, Martin, Alicia R., Daly, Mark J.

Get full text

Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation by Lo Faro, Valeria, Bhattacharya, Arjun, Zhou, Wei, Zhou, Dan, Wang, Ying, Läll, Kristi, Kanai, Masahiro, Lopera-Maya, Esteban, Straub, Peter, Pawar, Priyanka, Tao, Ran, Zhong, Xue, Namba, Shinichi, Sanna, Serena, Nolte, Ilja M., Okada, Yukinori, Ingold, Nathan, MacGregor, Stuart, Snieder, Harold, Surakka, Ida, Shortt, Jonathan, Gignoux, Chris, Rafaels, Nicholas, Crooks, Kristy, Verma, Anurag, Verma, Shefali S., Guare, Lindsay, Rader, Daniel J., Willer, Cristen, Martin, Alicia R., Brantley, Milam A., Gamazon, Eric R., Jansonius, Nomdo M., Joos, Karen, Cox, Nancy J., Hirbo, Jibril

Get full text

Editors' highlight picks from 2023 in EHJ Open by Bäck, Magnus, Banach, Maciej, Braunschweig, Frieder, De Rosa, Salvatore, Flachskampf, Frank A, Kahan, Thomas, Ketelhuth, Daniel F J, Lancellotti, Patrizio, Larsson, Susanna C, Mellbin, Linda, Nagy, Edit, Savarese, Gianluigi, Szummer, Karolina, Wahl, Denis

Get full text

Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts by Wang, Ying, Lopera, Esteban, Namba, Shinichi, Kerminen, Sini, Tsuo, Kristin, Läll, Kristi, Kanai, Masahiro, Zhou, Wei, Wu, Kuan-Han, Favé, Marie-Julie, Bhatta, Laxmi, Awadalla, Philip, Brumpton, Ben Michael, Deelen, Patrick, Hveem, Kristian, Faro, Valeria Lo, Mägi, Reedik, Murakami, Yoshinori, Sanna, Serena, Smoller, Jordan W, Uzunovic, Jasmina, Wolford, Brooke N, GBMI, Willer, Cristen, Gamazon, Eric R, Cox, Nancy J, Surakka, Ida, Okada, Yukinori, Martin, Alicia R, Hirbo, Jibril B

Request full text