Torthaí cuardaigh - Javed, Asif

A minimal descriptor of an ancestral recombinations graph de réir Parida, Laxmi, Palamara, Pier Francesco, Javed, Asif

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Lignin-Containing Coatings for Packaging Materials—Pilot Trials de réir Javed, Asif, Rättö, Peter, Järnström, Lars, Ullsten, Henrik

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NSIT: Novel Sequence Identification Tool de réir Pupacdi, Benjarath, Javed, Asif, Zaki, Mohammed J., Ruchirawat, Mathuros

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Minimizing recombinations in consensus networks for phylogeographic studies de réir Parida, Laxmi, Javed, Asif, Melé, Marta, Calafell, Francesc, Bertranpetit, Jaume

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A New Method to Reconstruct Recombination Events at a Genomic Scale de réir Melé, Marta, Javed, Asif, Pybus, Marc, Calafell, Francesc, Parida, Laxmi, Bertranpetit, Jaume

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Soil arsenic but not rice arsenic increasing with arsenic in irrigation water in the Punjab plains of Pakistan de réir Javed, Asif, Farooqi, Abida, Baig, Zakir Ullah, Ellis, Tyler, van Geen, Alexander

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One Step In-Situ Synthesis of Zinc Oxide Nanoparticles for Multifunctional Cotton Fabrics de réir Javed, Asif, Wiener, Jakub, Tamulevičienė, Asta, Tamulevičius, Tomas, Lazauskas, Algirdas, Saskova, Jana, Račkauskas, Simas

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Intra- and interpopulation genotype reconstruction from tagging SNPs de réir Paschou, Peristera, Mahoney, Michael W., Javed, Asif, Kidd, Judith R., Pakstis, Andrew J., Gu, Sheng, Kidd, Kenneth K., Drineas, Petros

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MITF variants cause nonsyndromic sensorineural hearing loss with autosomal recessive inheritance de réir Thongpradit, Supranee, Jinawath, Natini, Javed, Asif, Noojarern, Saisuda, Khongkraparn, Arthaporn, Tim-Aroon, Thipwimol, Lertsukprasert, Krisna, Suktitipat, Bhoom, Jensen, Laran T., Wattanasirichaigoon, Duangrurdee

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Occurrence of various viruses and recent evidence of SARS-CoV-2 in wastewater systems de réir Ali, Waqar, Zhang, Hua, Wang, Zhenglu, Chang, Chuanyu, Javed, Asif, Ali, Kamran, Du, Wei, Niazi, Nabeel Khan, Mao, Kang, Yang, Zhugen

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Validation and refinement of a RUNX1 mutation-associated gene expression signature in blast crisis chronic myeloid leukemia de réir Lee, Kian Leong, Ko, Tun Kiat, Saw, Nicole Y. L., Javed, Asif, Hillmer, Axel M., Chuah, Charles, Krishnan, Vaidehi, Ong, S. Tiong

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Novel SOX10 Mutations in Waardenburg Syndrome: Functional Characterization and Genotype-Phenotype Analysis de réir Thongpradit, Supranee, Jinawath, Natini, Javed, Asif, Jensen, Laran T., Chunsuwan, Issarapa, Rojnueangnit, Kitiwan, Tim-Aroon, Thipwimol, Lertsukprasert, Krisna, Shiao, Meng-Shin, Sirachainan, Nongnuch, Wattanasirichaigoon, Duangrurdee

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Experimental and bioinformatics considerations in cancer application of single cell genomics de réir Tan, Joanna Hui Juan, Kong, Say Li, Tai, Joyce A., Poh, Huay Mei, Yao, Fei, Sia, Yee Yen, Lim, Edwin Kok Hao, Takano, Angela Maria, Tan, Daniel Shao-Weng, Javed, Asif, Hillmer, Axel M.

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Incidentalome from Genomic Sequencing: A Barrier to Personalized Medicine? de réir Jamuar, Saumya Shekhar, Kuan, Jyn Ling, Brett, Maggie, Tiang, Zenia, Tan, Wilson Lek Wen, Lim, Jiin Ying, Liew, Wendy Kein Meng, Javed, Asif, Liew, Woei Kang, Law, Hai Yang, Tan, Ee Shien, Lai, Angeline, Ng, Ivy, Teo, Yik Ying, Venkatesh, Byrappa, Reversade, Bruno, Tan, Ene Choo, Foo, Roger

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Redefining prognostication of de novo cytogenetically normal acute myeloid leukemia in young adults de réir Tsui, Sze P., Ip, Ho W., Saw, Nicole Y., Zhang, Chunxiao, Cheung, Arthur K., Ng, Nelson K., Man, Cheuk H., Lam, Stephen S., Tang, Wing F., Lin, Chi H., Cheng, Grace H., Au, Chun H., Ma, Edmond S., Chan, Tsun L., So, Jason C., Ng, Margaret H., Cheng, Kelvin C., Wong, Kit F., Siu, Lai P., Yip, Sze F., Lin, Shek Y., Lau, June S., Luk, Tsan H., Lee, Harold K., Lau, Chi K., Kho, Bonnie, Sim, Joycelyn P., Kwong, Yok L., Leung, Suet Y., Javed, Asif, Leung, Anskar Y.

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Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness de réir Heilmann-Heimbach, Stefanie, Herold, Christine, Hochfeld, Lara M., Hillmer, Axel M., Nyholt, Dale R., Hecker, Julian, Javed, Asif, Chew, Elaine G. Y., Pechlivanis, Sonali, Drichel, Dmitriy, Heng, Xiu Ting, del Rosario, Ricardo C. -H., Fier, Heide L., Paus, Ralf, Rueedi, Rico, Galesloot, Tessel E., Moebus, Susanne, Anhalt, Thomas, Prabhakar, Shyam, Li, Rui, Kanoni, Stavroula, Papanikolaou, George, Kutalik, Zoltán, Deloukas, Panos, Philpott, Michael P., Waeber, Gérard, Spector, Tim D., Vollenweider, Peter, Kiemeney, Lambertus A. L. M., Dedoussis, George, Richards, J. Brent, Nothnagel, Michael, Martin, Nicholas G., Becker, Tim, Hinds, David A., Nöthen, Markus M.

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ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder de réir Williams, Lloyd B., Javed, Asif, Sabri, Amin, Morgan, Denise J., Huff, Chad D., Grigg, John R., Heng, Xiu Ting, Khng, Alexis J., Hollink, Iris H. I. M., Morrison, Margaux A., Owen, Leah A., Anderson, Katherine, Kinard, Krista, Greenlees, Rebecca, Novacic, Danica, Nida Sen, H., Zein, Wadih M., Rodgers, George M., Vitale, Albert T., Haider, Neena B., Hillmer, Axel M., Ng, Pauline C., Shankaracharya, Cheng, Anson, Zheng, Linda, Gillies, Mark C., van Slegtenhorst, Marjon, van Hagen, P. Martin, Missotten, Tom O. A. R., Farley, Gary L., Polo, Michael, Malatack, James, Curtin, Julie, Martin, Frank, Arbuckle, Susan, Alexander, Stephen I., Chircop, Megan, Davila, Sonia, Digre, Kathleen B., Jamieson, Robyn V., DeAngelis, Margaret M.

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Y-chromosome analysis reveals genetic divergence and new founding native lineages in Athapaskan- and Eskimoan-speaking populations de réir Dulik, Matthew C., Owings, Amanda C., Gaieski, Jill B., Vilar, Miguel G., Andre, Alestine, Lennie, Crystal, Mackenzie, Mary Adele, Kritsch, Ingrid, Snowshoe, Sharon, Wright, Ruth, Martin, James, Gibson, Nancy, Andrews, Thomas D., Schurr, Theodore G., Adhikarla, Syama, Adler, Christina J., Balanovska, Elena, Balanovsky, Oleg, Bertranpetit, Jaume, Clarke, Andrew C., Comas, David, Cooper, Alan, Der Sarkissian, Clio S. I., GaneshPrasad, ArunKumar, Haak, Wolfgang, Haber, Marc, Hobbs, Angela, Javed, Asif, Jin, Li, Kaplan, Matthew E., Li, Shilin, Martínez-Cruz, Begoña, Matisoo-Smith, Elizabeth A., Melé, Marta, Merchant, Nirav C., Mitchell, R. John, Parida, Laxmi, Pitchappan, Ramasamy, Platt, Daniel E., Quintana-Murci, Lluis, Renfrew, Colin, Lacerda, Daniela R., Royyuru, Ajay K., Santos, Fabrício R., Soodyall, Himla, Soria Hernanz, David F., Swamikrishnan, Pandikumar, Tyler-Smith, Chris, Santhakumari, Arun Varatharajan, Vieira, Pedro Paulo, Wells, R. Spencer, Zalloua, Pierre A., Ziegle, Janet S.

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An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge de réir Brownstein, Catherine A, Beggs, Alan H, Homer, Nils, Merriman, Barry, Yu, Timothy W, Flannery, Katherine C, DeChene, Elizabeth T, Towne, Meghan C, Savage, Sarah K, Price, Emily N, Holm, Ingrid A, Luquette, Lovelace J, Lyon, Elaine, Majzoub, Joseph, Neupert, Peter, McCallie Jr, David, Szolovits, Peter, Willard, Huntington F, Mendelsohn, Nancy J, Temme, Renee, Finkel, Richard S, Yum, Sabrina W, Medne, Livija, Sunyaev, Shamil R, Adzhubey, Ivan, Cassa, Christopher A, de Bakker, Paul IW, Duzkale, Hatice, Dworzyński, Piotr, Fairbrother, William, Francioli, Laurent, Funke, Birgit H, Giovanni, Monica A, Handsaker, Robert E, Lage, Kasper, Lebo, Matthew S, Lek, Monkol, Leshchiner, Ignaty, MacArthur, Daniel G, McLaughlin, Heather M, Murray, Michael F, Pers, Tune H, Polak, Paz P, Raychaudhuri, Soumya, Rehm, Heidi L, Soemedi, Rachel, Stitziel, Nathan O, Vestecka, Sara, Supper, Jochen, Gugenmus, Claudia, Klocke, Bernward, Hahn, Alexander, Schubach, Max, Menzel, Mortiz, Biskup, Saskia, Freisinger, Peter, Deng, Mario, Braun, Martin, Perner, Sven, Smith, Richard JH, Andorf, Janeen L, Huang, Jian, Ryckman, Kelli, Sheffield, Val C, Stone, Edwin M, Bair, Thomas, Black-Ziegelbein, E Ann, Braun, Terry A, Darbro, Benjamin, DeLuca, Adam P, Kolbe, Diana L, Scheetz, Todd E, Shearer, Aiden E, Sompallae, Rama, Wang, Kai, Bassuk, Alexander G, Edens, Erik, Mathews, Katherine, Moore, Steven A, Shchelochkov, Oleg A, Trapane, Pamela, Bossler, Aaron, Campbell, Colleen A, Heusel, Jonathan W, Kwitek, Anne, Maga, Tara, Panzer, Karin, Wassink, Thomas, Van Daele, Douglas, Azaiez, Hela, Booth, Kevin, Meyer, Nic, Segal, Michael M, Williams, Marc S, Tromp, Gerard, White, Peter, Corsmeier, Donald, Fitzgerald-Butt, Sara, Herman, Gail, Lamb-Thrush, Devon, McBride, Kim L, Newsom, David, Pierson, Christopher R, Rakowsky, Alexander T, Maver, Aleš, Lovrečić, Luca, Palandačić, Anja, Peterlin, Borut, Torkamani, Ali, Wedell, Anna, Huss, Mikael, Alexeyenko, Andrey, Lindvall, Jessica M, Magnusson, Måns, Nilsson, Daniel, Stranneheim, Henrik, Taylan, Fulya, Gilissen, Christian, Hoischen, Alexander, van Bon, Bregje, Yntema, Helger, Nelen, Marcel, Zhang, Weidong, Sager, Jason, Zhang, Lu, Blair, Kathryn, Kural, Deniz, Cariaso, Michael, Lennon, Greg G, Javed, Asif, Agrawal, Saloni, Ng, Pauline C, Sandhu, Komal S, Krishna, Shuba, Veeramachaneni, Vamsi, Isakov, Ofer, Halperin, Eran, Friedman, Eitan, Shomron, Noam, Glusman, Gustavo, Roach, Jared C, Caballero, Juan, Cox, Hannah C, Mauldin, Denise, Ament, Seth A, Rowen, Lee, Richards, Daniel R, Lucas, F Anthony San, Gonzalez-Garay, Manuel L, Caskey, C Thomas, Bai, Yu, Huang, Ying, Fang, Fang, Zhang, Yan, Wang, Zhengyuan, Barrera, Jorge, Garcia-Lobo, Juan M, González-Lamuño, Domingo, Llorca, Javier, Rodriguez, Maria C, Varela, Ignacio, Reese, Martin G, De La Vega, Francisco M, Kiruluta, Edward, Cargill, Michele, Hart, Reece K, Sorenson, Jon M, Lyon, Gholson J, Stevenson, David A, Bray, Bruce E, Moore, Barry M, Eilbeck, Karen, Yandell, Mark, Zhao, Hongyu, Hou, Lin, Chen, Xiaowei, Yan, Xiting, Chen, Mengjie, Li, Cong, Yang, Can, Gunel, Murat, Li, Peining, Kong, Yong, Alexander, Austin C, Albertyn, Zayed I, Boycott, Kym M, Bulman, Dennis E, Gordon, Paul MK, Innes, A Micheil, Knoppers, Bartha M, Majewski, Jacek, Marshall, Christian R, Parboosingh, Jillian S, Sawyer, Sarah L, Samuels, Mark E, Schwartzentruber, Jeremy, Kohane, Isaac S, Margulies, David M

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