Výsledky vyhledávání - Guha, Saurav

Development of novel heminested PCR assays based on mitochondrial 16s rRNA gene for identification of seven pecora species Autor Guha, Saurav, Kashyap, VK

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Multivariate Small Area Modelling for Measuring Micro Level Earning Inequality: Evidence from Periodic Labour Force Survey of India Autor Guha, Saurav, Chandra, Hukum

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Genetic structure of Indian populations based on fifteen autosomal microsatellite loci Autor Kashyap, VK, Guha, Saurav, Sitalaximi, T, Bindu, G Hima, Hasnain, Seyed E, Trivedi, R

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Excess of homozygosity in the major histocompatibility complex in schizophrenia Autor Mukherjee, Semanti, Guha, Saurav, Ikeda, Masashi, Iwata, Nakao, Malhotra, Anil K., Pe'er, Itsik, Darvasi, Ariel, Lencz, Todd

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A Schizophrenia Risk Gene, ZNF804A, is Associated with Brain White Matter Microstructure Autor Ikuta, Toshikazu, Peters, Bart D., Guha, Saurav, John, Majnu, Karlsgodt, Katherine H., Lencz, Todd, Szeszko, Philip R., Malhotra, Anil K.

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Common Variants in 8q24 and MYC Oncogene are Associated with Risk for Prostate Cancer and Tumor Aggressiveness in Men of European Ancestry Autor Pal, Prodipto, Xi, Huifeng, Guha, Saurav, Sun, Guangyun, Helfand, Brian T., Meeks, Joshua J., Suarez, Brian K., Catalona, William J., Deka, Ranjan

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Implications for health and disease in the genetic signature of the Ashkenazi Jewish population Autor Guha, Saurav, Rosenfeld, Jeffrey A, Malhotra, Anil K, Lee, Annette T, Gregersen, Peter K, Kane, John M, Pe'er, Itsik, Darvasi, Ariel, Lencz, Todd

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Association of Tagging Single Nucleotide Polymorphisms on 8 Candidate Genes in Dopaminergic Pathway with Schizophrenia in Croatian Population Autor Pal, Prodipto, Mihanović, Mate, Molnar, Sven, Xi, Huifeng, Sun, Guangyun, Guha, Saurav, Jeran, Nina, Tomljenović, Andrea, Malnar, Ana, Missoni, Saša, Deka, Ranjan, Rudan, Pavao

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Brain White Matter Development Is Associated with a Human-Specific Haplotype Increasing the Synthesis of Long Chain Fatty Acids Autor Peters, Bart D., Voineskos, Aristotle N., Szeszko, Philip R., Lett, Tristram A., DeRosse, Pamela, Guha, Saurav, Karlsgodt, Katherine H., Ikuta, Toshikazu, Felsky, Daniel, John, Majnu, Rotenberg, David J., Kennedy, James L., Lencz, Todd, Malhotra, Anil K.

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Genetic Variants Associated with Breast Cancer Risk for Ashkenazi Jewish Women with Strong Family Histories but No Identifiable BRCA1/2 Mutation Autor Rinella, Erica S., Shao, Yongzhao, Yackowski, Lauren, Pramanik, Sreemanta, Oratz, Ruth, Schnabel, Freya, Guha, Saurav, LeDuc, Charles, Campbell, Chris, Klugman, Susan D., Terry, Mary Beth, Senie, Ruby T., Andrulis, Irene L., Daly, Mary, John, Esther M., Roses, Daniel, Chung, Wendy K., Ostrer, Harry

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De novo copy number variants are associated with congenital diaphragmatic hernia Autor Yu, Lan, Wynn, Julia, Ma, Lijiang, Guha, Saurav, Mychaliska, George B., Crombleholme, Timothy M., Azarow, Kenneth S., Lim, Foong Yen, Chung, Dai H., Potoka, Douglas, Warner, Brad W., Bucher, Brian, LeDuc, Charles A., Costa, Katherine, Stolar, Charles, Aspelund, Gudrun, Arkovitz, Marc, Chung, Wendy K.

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Best practices for the interpretation and reporting of clinical whole genome sequencing Autor Austin-Tse, Christina A., Jobanputra, Vaidehi, Perry, Denise L., Bick, David, Taft, Ryan J., Venner, Eric, Gibbs, Richard A., Young, Ted, Barnett, Sarah, Belmont, John W., Boczek, Nicole, Chowdhury, Shimul, Ellsworth, Katarzyna A., Guha, Saurav, Kulkarni, Shashikant, Marcou, Cherisse, Meng, Linyan, Murdock, David R., Rehman, Atteeq U., Spiteri, Elizabeth, Thomas-Wilson, Amanda, Kearney, Hutton M., Rehm, Heidi L.

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Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder Autor Lencz, Todd, Guha, Saurav, Liu, Chunyu, Rosenfeld, Jeffrey, Mukherjee, Semanti, DeRosse, Pamela, John, Majnu, Cheng, Lijun, Zhang, Chunling, Badner, Judith A., Ikeda, Masashi, Iwata, Nakao, Cichon, Sven, Rietschel, Marcella, Nöthen, Markus M., Cheng, A.T.A., Hodgkinson, Colin, Yuan, Qiaoping, Kane, John M., Lee, Annette T., Pisanté, Anne, Gregersen, Peter K., Pe’er, Itsik, Malhotra, Anil K., Goldman, David, Darvasi, Ariel

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Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes Autor Vacic, Vladimir, Ozelius, Laurie J., Clark, Lorraine N., Bar-Shira, Anat, Gana-Weisz, Mali, Gurevich, Tanya, Gusev, Alexander, Kedmi, Merav, Kenny, Eimear E., Liu, Xinmin, Mejia-Santana, Helen, Mirelman, Anat, Raymond, Deborah, Saunders-Pullman, Rachel, Desnick, Robert J., Atzmon, Gil, Burns, Edward R., Ostrer, Harry, Hakonarson, Hakon, Bergman, Aviv, Barzilai, Nir, Darvasi, Ariel, Peter, Inga, Guha, Saurav, Lencz, Todd, Giladi, Nir, Marder, Karen, Pe'er, Itsik, Bressman, Susan B., Orr-Urtreger, Avi

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Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins Autor Carmi, Shai, Hui, Ken Y., Kochav, Ethan, Liu, Xinmin, Xue, James, Grady, Fillan, Guha, Saurav, Upadhyay, Kinnari, Ben-Avraham, Dan, Mukherjee, Semanti, Bowen, B. Monica, Thomas, Tinu, Vijai, Joseph, Cruts, Marc, Froyen, Guy, Lambrechts, Diether, Plaisance, Stéphane, Van Broeckhoven, Christine, Van Damme, Philip, Van Marck, Herwig, Barzilai, Nir, Darvasi, Ariel, Offit, Kenneth, Bressman, Susan, Ozelius, Laurie J., Peter, Inga, Cho, Judy H., Ostrer, Harry, Atzmon, Gil, Clark, Lorraine N., Lencz, Todd, Pe’er, Itsik

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Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies Autor Amendola, Laura M., Muenzen, Kathleen, Biesecker, Leslie G., Bowling, Kevin M., Cooper, Greg M., Dorschner, Michael O., Driscoll, Catherine, Foreman, Ann Katherine M., Golden-Grant, Katie, Greally, John M., Hindorff, Lucia, Kanavy, Dona, Jobanputra, Vaidehi, Johnston, Jennifer J., Kenny, Eimear E., McNulty, Shannon, Murali, Priyanka, Ou, Jeffrey, Powell, Bradford C., Rehm, Heidi L., Rolf, Bradley, Roman, Tamara S., Van Ziffle, Jessica, Guha, Saurav, Abhyankar, Avinash, Crosslin, David, Venner, Eric, Yuan, Bo, Zouk, Hana, Jarvik, Gail P.

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Molecular Genetic Evidence for Genetic Overlap between General Cognitive Ability and Risk for Schizophrenia: A Report from the Cognitive Genomics Consortium (COGENT) Autor Lencz, Todd, Knowles, Emma, Davies, Gail, Guha, Saurav, Liewald, David C, Starr, John M, Djurovic, Srdjan, Melle, Ingrid, Sundet, Kjetil, Christoforou, Andrea, Reinvang, Ivar, Mukherjee, Semanti, Lundervold, Astri, Steen, Vidar M., John, Majnu, Espeseth, Thomas, Räikkönen, Katri, Widen, Elisabeth, Palotie, Aarno, Eriksson, Johan G, Giegling, Ina, Konte, Bettina, Ikeda, Masashi, Roussos, Panos, Giakoumaki, Stella, Burdick, Katherine E., Payton, Antony, Ollier, William, Horan, Mike, Donohoe, Gary, Morris, Derek, Corvin, Aiden, Gill, Michael, Pendleton, Neil, Iwata, Nakao, Darvasi, Ariel, Bitsios, Panos, Rujescu, Dan, Lahti, Jari, Hellard, Stephanie Le, Keller, Matthew C., Andreassen, Ole A., Deary, Ian J, Glahn, David C., Malhotra, Anil K.

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Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel Autor Shen, Jun, Oza, Andrea M., del Castillo, Ignacio, Duzkale, Hatice, Matsunaga, Tatsuo, Pandya, Arti, Kang, Hyunseok P., Mar-Heyming, Rebecca, Guha, Saurav, Moyer, Krista, Lo, Christine, Kenna, Margaret, Alexander, John J., Zhang, Yan, Hirsch, Yoel, Luo, Minjie, Cao, Ye, Choy, Kwong Wai, Cheng, Yen-Fu, Avraham, Karen B., Hu, Xinhua, Garrido, Gema, Moreno-Pelayo, Miguel A., Greinwald, John, Zhang, Kejian, Zeng, Yukun, Brownstein, Zippora, Basel-Salmon, Lina, Davidov, Bella, Frydman, Moshe, Weiden, Tzvi, Nagan, Narasimhan, Willis, Alecia, Hemphill, Sarah E., Grant, Andrew R., Siegert, Rebecca K., DiStefano, Marina T., Amr, Sami S., Rehm, Heidi L., Tayoun, Ahmad N. Abou

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A rare deletion at distal 16p11.2 is implicated in schizophrenia Autor Guha, Saurav, Rees, Elliott, Darvasi, Ariel, Ivanov, Dobril, Ikeda, Masashi, Bergen, Sarah E., Magnusson, Patrik K, Cormican, Paul, Morris, Derek, Gill, Michael, Cichon, Sven, Rosenfeld, Jeffrey A., Lee, Annette, Gregersen, Peter K., Kane, John M., Malhotra, Anil K., Rietschel, Marcella, Nöthen, Markus M., Degenhardt, Franziska, Priebe, Lutz, Breuer, René, Strohmaier, Jana, Ruderfer, Douglas M, Moran, Jennifer L, Chambert, Kimberly D, Sanders, Alan R., Shi, Jianxin, Kendler, Kenneth, Riley, Brien, O’Neill, Tony, Walsh, Dermot, Malhotra, Dheeraj, Corvin, Aiden, Purcell, Shaun, Sklar, Pamela, Iwata, Nakao, Hultman, Christina M, Sullivan, Patrick F., Sebat, Jonathan, McCarthy, Shane, Gejman, Pablo V., Levinson, Douglas F., Owen, Michael J, O’Donovan, Michael C, Lencz, Todd, Kirov, George

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Independent Evidence for an Association between General Cognitive Ability and a Genetic Locus for Educational Attainment Autor Trampush, Joey W., Lencz, Todd, Knowles, Emma, Davies, Gail, Guha, Saurav, Pe’er, Itsik, Liewald, David C., Starr, John M., Djurovic, Srdjan, Melle, Ingrid, Sundet, Kjetil, Christoforou, Andrea, Reinvang, Ivar, Mukherjee, Semanti, DeRosse, Pamela, Lundervold, Astri, Steen, Vidar M., John, Majnu, Espeseth, Thomas, Räikkönen, Katri, Widen, Elisabeth, Palotie, Aarno, Eriksson, Johan G., Giegling, Ina, Konte, Bettina, Ikeda, Masashi, Roussos, Panos, Giakoumaki, Stella, Burdick, Katherine E., Payton, Antony, Ollier, William, Horan, Mike, Scult, Matthew, Dickinson, Dwight, Straub, Richard E., Donohoe, Gary, Morris, Derek, Corvin, Aiden, Gill, Michael, Hariri, Ahmad, Weinberger, Daniel R., Pendleton, Neil, Iwata, Nakao, Darvasi, Ariel, Bitsios, Panos, Rujescu, Dan, Lahti, Jari, Le Hellard, Stephanie, Keller, Matthew C., Andreassen, Ole A., Deary, Ian J., Glahn, David C., Malhotra, Anil K.

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