Coordinated Conditional Simulation with SLINK and SUP of Many Markers Linked or Associated to a Trait in Large Pedigrees

Por Schäffer, Alejandro A., Lemire, Mathieu, Ott, Jürg, Lathrop, G. Mark, Weeks, Daniel E.
Publicado em 2011

Mapping Approaches to Gene Identification in Humans

Por White, Raymond L., Lalouel, Jean-Marc, Lathrop, G. Mark, Leppert, Mark F., Nakamura, Yusuke, O'Connell, Peter
Publicado em 1987

A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines

Por Liang, Liming, Morar, Nilesh, Dixon, Anna L., Lathrop, G. Mark, Abecasis, Goncalo R., Moffatt, Miriam F., Cookson, William O.C.
Publicado em 2013

Further linkage data on cystic fibrosis: The utah study

Por White, Ray, Leppert, Mark, O'Connell, Peter, Nakamura, Yusuke, Woodward, Scott, Hoff, Mark, Herbst, John, Dean, Michael, Woude, George Vande, Lathrop, G. Mark, Lalouel, Jean-Marc
Publicado em 1986

Genetic and Haplotypic Structure in 14 European and African Cattle Breeds

Por Gautier, Mathieu, Faraut, Thomas, Moazami-Goudarzi, Katayoun, Navratil, Vincent, Foglio, Mario, Grohs, Cécile, Boland, Anne, Garnier, Jean-Guillaume, Boichard, Didier, Lathrop, G. Mark, Gut, Ivo G., Eggen, André
Publicado em 2007

Integrating Pathway Analysis and Genetics of Gene Expression for Genome-wide Association Study of Basal Cell Carcinoma

Por Zhang, Mingfeng, Liang, Liming, Morar, Nilesh, Dixon, Anna L, Lathrop, G Mark, Ding, Jun, Moffatt, Miriam F, Cookson, William O C, Kraft, Peter, Qureshi, Abrar A., Han, Jiali
Publicado em 2011

eQTL mapping identify insertion and deletion specific eQTLs in multiple tissues

Por Huang, Jinyan, Chen, Jun, Esparza, Jorge, Ding, Jun, Elder, James, Abecasis, Goncalo R, Lee, Young-Ae, Lathrop, G. Mark, Moffatt, Miriam F, Cookson, William O C, Liang, Liming
Publicado no Nat Commun (2015)

Aristolochic acid exposure in Romania and implications for renal cell carcinoma

Por Turesky, Robert J, Yun, Byeong Hwa, Brennan, Paul, Mates, Dana, Jinga, Viorel, Harnden, Patricia, Banks, Rosamonde E, Blanche, Helene, Bihoreau, Marie-Therese, Chopard, Priscilia, Letourneau, Louis, Lathrop, G Mark, Scelo, Ghislaine
Publicado no Br J Cancer (2016)

A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates

Por Buetow, Kenneth H., Shiang, Rita, Yang, Ping, Nakamura, Yusuke, Lathrop, G. Mark, White, Raymond, Wasmuth, John J., Wood, Stephen, Berdahl, Laura D., Leysens, Nancy J., Ritty, Timothy M., Wise, Molly E., Murray, Jeffrey C.
Publicado em 1991

Infantile Convulsions with Paroxysmal Dyskinesia (ICCA Syndrome) and Copy Number Variation at Human Chromosome 16p11

Por Roll, Patrice, Sanlaville, Damien, Cillario, Jennifer, Labalme, Audrey, Bruneau, Nadine, Massacrier, Annick, Délepine, Marc, Dessen, Philippe, Lazar, Vladimir, Robaglia-Schlupp, Andrée, Lesca, Gaëtan, Jouve, Elisabeth, Rudolf, Gabrielle, Rochette, Jacques, Lathrop, G. Mark, Szepetowski, Pierre
Publicado em 2010

Fine mapping of eight psoriasis susceptibility loci

Por Das, Sayantan, Stuart, Philip E, Ding, Jun, Tejasvi, Trilokraj, Li, Yanming, Tsoi, Lam C, Chandran, Vinod, Fischer, Judith, Helms, Cynthia, Duffin, Kristina Callis, Voorhees, John J, Bowcock, Anne M, Krueger, Gerald G, Lathrop, G Mark, Nair, Rajan P, Rahman, Proton, Abecasis, Goncalo R, Gladman, Dafna, Elder, James T
Publicado no Eur J Hum Genet (2015)

Linkage Analysis Using Co-Phenotypes in the BRIGHT Study Reveals Novel Potential Susceptibility Loci for Hypertension

Por Wallace, Chris, Xue, Ming-Zhan, Newhouse, Stephen J., Marçano, Ana Carolina B., Onipinla, Abiodun K., Burke, Beverley, Gungadoo, Johannie, Dobson, Richard J., Brown, Morris, Connell, John M., Dominiczak, Anna, Lathrop, G. Mark, Webster, John, Farrall, Martin, Mein, Charles, Samani, Nilesh J., Caulfield, Mark J., Clayton, David G., Munroe, Patricia B.
Publicado em 2006

Genome-wide Association Study Identifies Genes for Biomarkers of Cardiovascular Disease: Serum Urate and Dyslipidemia

Por Wallace, Chris, Newhouse, Stephen J., Braund, Peter, Zhang, Feng, Tobin, Martin, Falchi, Mario, Ahmadi, Kourosh, Dobson, Richard J., Marçano, Ana Carolina B., Hajat, Cother, Burton, Paul, Deloukas, Panagiotis, Brown, Morris, Connell, John M., Dominiczak, Anna, Lathrop, G. Mark, Webster, John, Farrall, Martin, Spector, Tim, Samani, Nilesh J., Caulfield, Mark J., Munroe, Patricia B.
Publicado em 2008

An Epigenome-Wide Association Study of Total Serum Immunoglobulin E Concentration

Por Liang, Liming, Willis-Owen, Saffron A.G., Laprise, Catherine, Wong, Kenny C.C., Davies, Gwyneth A., Hudson, Thomas J., Binia, Aristea, Hopkin, Julian M., Yang, Ivana V., Grundberg, Elin, Busche, Stephan, Hudson, Marie, Rönnblom, Lars, Pastinen, Tomi M., Schwartz, David A., Lathrop, G. Mark, Moffatt, Miriam F., Cookson, William O.C.M.
Publicado no Nature (2015)

A Genomewide Scan for Loci Predisposing to Type 2 Diabetes in a U.K. Population (The Diabetes UK Warren 2 Repository): Analysis of 573 Pedigrees Provides Independent Replication of...

Por Wiltshire, Steven, Hattersley, Andrew T., Hitman, Graham A., Walker, Mark, Levy, Jonathan C., Sampson, Michael, O’Rahilly, Stephen, Frayling, Timothy M., Bell, John I., Lathrop, G. Mark, Bennett, Amanda, Dhillon, Ranjit, Fletcher, Christopher, Groves, Christopher J., Jones, Elizabeth, Prestwich, Philip, Simecek, Nikol, Rao, Pamidighantam V. Subba, Wishart, Marie, Foxon, Richard, Howell, Simon, Smedley, Damian, Cardon, Lon R., Menzel, Stephan, McCarthy, Mark I.
Publicado em 2001

Genomewide Scan Reveals Association of Psoriasis with IL-23 and NF-κB Pathways

Por Nair, Rajan P., Duffin, Kristina Callis, Helms, Cindy, Ding, Jun, Stuart, Philip E., Goldgar, David, Gudjonsson, Johann E., Li, Yun, Tejasvi, Trilokraj, Feng, Bing Jian, Ruether, Andreas, Schreiber, Stefan, Weichenthal, Michael, Gladman, Dafna, Rahman, Proton, Schrodi, Steven J., Prahalad, Sampath, Guthery, Stephen L, Fischer, Judith, Liao, Wilson, Kwok, Pui-Yan, Menter, Alan, Lathrop, G. Mark, Wise, Carol A., Begovich, Ann B., Voorhees, John J., Elder, James T., Krueger, Gerald G., Bowcock, Anne M., Abecasis, Gonçalo R.
Publicado em 2009

Polymorphisms in the WNK1 Gene Are Associated with Blood Pressure Variation and Urinary Potassium Excretion

Por Newhouse, Stephen, Farrall, Martin, Wallace, Chris, Hoti, Mimoza, Burke, Beverley, Howard, Philip, Onipinla, Abiodun, Lee, Kate, Shaw-Hawkins, Sue, Dobson, Richard, Brown, Morris, Samani, Nilesh J., Dominiczak, Anna F., Connell, John M., Lathrop, G. Mark, Kooner, Jaspal, Chambers, John, Elliott, Paul, Clarke, Robert, Collins, Rory, Laan, Maris, Org, Elin, Juhanson, Peeter, Veldre, Gudrun, Viigimaa, Margus, Eyheramendy, Susana, Cappuccio, Francesco P., Ji, Chen, Iacone, Roberto, Strazzullo, Pasquale, Kumari, Meena, Marmot, Michael, Brunner, Eric, Caulfield, Mark, Munroe, Patricia B.
Publicado em 2009

SLC2A9 Is a High-Capacity Urate Transporter in Humans

Por Caulfield, Mark J, Munroe, Patricia B, O'Neill, Deb, Witkowska, Kate, Charchar, Fadi J, Doblado, Manuel, Evans, Sarah, Eyheramendy, Susana, Onipinla, Abiodun, Howard, Philip, Shaw-Hawkins, Sue, Dobson, Richard J, Wallace, Chris, Newhouse, Stephen J, Brown, Morris, Connell, John M, Dominiczak, Anna, Farrall, Martin, Lathrop, G. Mark, Samani, Nilesh J, Kumari, Meena, Marmot, Michael, Brunner, Eric, Chambers, John, Elliott, Paul, Kooner, Jaspal, Laan, Maris, Org, Elin, Veldre, Gudrun, Viigimaa, Margus, Cappuccio, Francesco P, Ji, Chen, Iacone, Roberto, Strazzullo, Pasquale, Moley, Kelle H, Cheeseman, Chris
Publicado em 2008

A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis

Por Weidinger, Stephan, Willis-Owen, Saffron A.G., Kamatani, Yoichiro, Baurecht, Hansjörg, Morar, Nilesh, Liang, Liming, Edser, Pauline, Street, Teresa, Rodriguez, Elke, O'Regan, Grainne M., Beattie, Paula, Fölster-Holst, Regina, Franke, Andre, Novak, Natalija, Fahy, Caoimhe M., Winge, Mårten C.G., Kabesch, Michael, Illig, Thomas, Heath, Simon, Söderhäll, Cilla, Melén, Erik, Pershagen, Göran, Kere, Juha, Bradley, Maria, Lieden, Agne, Nordenskjold, Magnus, Harper, John I., Mclean, W.H. Irwin, Brown, Sara J., Cookson, William O.C., Lathrop, G. Mark, Irvine, Alan D., Moffatt, Miriam F.
Publicado em 2013

Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot

Por Cordell, Heather J., Töpf, Ana, Mamasoula, Chrysovalanto, Postma, Alex V., Bentham, Jamie, Zelenika, Diana, Heath, Simon, Blue, Gillian, Cosgrove, Catherine, Granados Riveron, Javier, Darlay, Rebecca, Soemedi, Rachel, Wilson, Ian J., Ayers, Kristin L., Rahman, Thahira J., Hall, Darroch, Mulder, Barbara J.M., Zwinderman, Aelko H., van Engelen, Klaartje, Brook, J. David, Setchfield, Kerry, Bu'Lock, Frances A., Thornborough, Chris, O'Sullivan, John, Stuart, A. Graham, Parsons, Jonathan, Bhattacharya, Shoumo, Winlaw, David, Mital, Seema, Gewillig, Marc, Breckpot, Jeroen, Devriendt, Koen, Moorman, Antoon F.M., Rauch, Anita, Lathrop, G. Mark, Keavney, Bernard D., Goodship, Judith A.
Publicado em 2013