检索结果 - Guha, Saurav

Development of novel heminested PCR assays based on mitochondrial 16s rRNA gene for identification of seven pecora species 由 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 由 Guha, Saurav, Chandra, Hukum

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Genetic structure of Indian populations based on fifteen autosomal microsatellite loci 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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) 由 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 由 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 由 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 由 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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