TDT-HET: A new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data

Por Londono, Douglas, Buyske, Steven, Finch, Stephen J, Sharma, Swarkar, Wise, Carol A, Gordon, Derek
Publicado em 2012

Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities

Por Musolf, Anthony, Nato, Alejandro Q, Londono, Douglas, Zhou, Lisheng, Matise, Tara C, Gordon, Derek
Publicado em 2014

An analytic solution to computation of power and sample size for genetic association studies under a pleiotropic mode of inheritance

Por Gordon, Derek, Londono, Douglas, Patel, Payal, Kim, Wonkuk, Finch, Stephen J., Heiman, Gary A.
Publicado no Hum Hered (2017)

Evidence for association of two variants of the nociceptin/orphanin FQ receptor gene OPRL1 with vulnerability to develop opiate addiction in Caucasians

Por Briant, Judith A., Nielsen, David A., Proudnikov, Dmitri, Londono, Douglas, Ho, Ann, Ott, Jurg, Kreek, Mary Jeanne
Publicado em 2010

Single variant and multi-variant trend tests for genetic association with next generation sequencing that are robust to sequencing error

Por Kim, Wonkuk, Londono, Douglas, Zhou, Lisheng, Xing, Jinchuan, Nato, Andrew, Musolf, Anthony, Matise, Tara C., Finch, Stephen J., Gordon, Derek
Publicado em 2013

Heroin addiction in African Americans: a hypothesis-driven association study

Por Levran, Orna, Londono, Douglas, O'Hara, Kim, Randesi, Matthew, Rotrosen, John, Casadonte, Paul, Linzy, Shirley, Ott, Jurg, Adelson, Miriam, Kreek, Mary Jeanne
Publicado em 2009

Density-based clustering in haplotype analysis for association mapping

Por Igo, Robert P, Londono, Douglas, Miller, Katherine, Parrado, Antonio R, Quade, Shannon RE, Sinha, Moumita, Kim, Sulgi, Won, Sungho, Li, Jing, Goddard, Katrina AB
Publicado em 2007

IL-18R1 and IL-18RAP SNPs may associate with Bronchopulmonary Dysplasia in African American infants

Por Floros, Joanna, Londono, Douglas, Gordon, Derek, Silveyra, Patricia, Diangelo, Susan L, Viscardi, Rose M, Worthen, George S, Shenberger, Jeffrey, Wang, Guirong, Lin, Zhenwu, Thomas, Neal J
Publicado em 2012

Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata

Por Martinez-Mir, Amalia , Zlotogorski, Abraham , Gordon, Derek , Petukhova, Lynn , Mo, Jianhong , Gilliam, T. Conrad , Londono, Douglas , Haynes, Chad , Ott, Jurg , Hordinsky, Maria , Nanova, Krassimira , Norris, David , Price, Vera , Duvic, Madeleine , Christiano, Angela M. 
Publicado em 2007

Bone marrow-derived epithelial cells and hair follicle stem cells contribute to development of chronic cutaneous neoplasms

Por Park, Heuijoon, Lad, Sonali, Boland, Kelsey, Johnson, Kelly, Readio, Nyssa, Jin, Guangchun, Asfaha, Samuel, Patterson, Kelly S., Singh, Ashok, Yang, Xiangdong, Londono, Douglas, Singh, Anupama, Trempus, Carol, Gordon, Derek, Wang, Timothy C., Morris, Rebecca J.
Publicado no Nat Commun (2018)

A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females

Por Sharma, Swarkar, Londono, Douglas, Eckalbar, Walter L., Gao, Xiaochong, Zhang, Dongping, Mauldin, Kristen, Kou, Ikuyo, Takahashi, Atsushi, Matsumoto, Morio, Kamiya, Nobuhiro, Murphy, Karl K., Cornelia, Reuel, Herring, John A., Burns, Dennis, Ahituv, Nadav, Ikegawa, Shiro, Gordon, Derek, Wise, Carol A.
Publicado no Nat Commun (2015)

Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes

Por Sharma, Swarkar, Gao, Xiaochong, Londono, Douglas, Devroy, Shonn E., Mauldin, Kristen N., Frankel, Jessica T., Brandon, January M., Zhang, Dongping, Li, Quan-Zhen, Dobbs, Matthew B., Gurnett, Christina A., Grant, Struan F.A., Hakonarson, Hakon, Dormans, John P., Herring, John A., Gordon, Derek, Wise, Carol A.
Publicado em 2011

Chromatin Profiling Reveals Regulatory Network Shifts and a Protective Role for Hepatocyte Nuclear Factor 4α during Colitis

Por Chahar, Sanjay, Gandhi, Vishal, Yu, Shiyan, Desai, Kinjal, Cowper-Sal·lari, Richard, Kim, Yona, Perekatt, Ansu O., Kumar, Namit, Thackray, Joshua K., Musolf, Anthony, Kumar, Nikhil, Hoffman, A., Londono, Douglas, Vazquez, Berta N., Serrano, Lourdes, Shin, Hyunjin, Lupien, Mathieu, Gao, Nan, Verzi, Michael P.
Publicado em 2014

EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity

Por Darrah, Rebecca, McKone, Edward, O'Connor, Clare, Rodgers, Christine, Genatossio, Alan, McNamara, Sharon, Gibson, Ronald, Stuart Elborn, J., Ennis, Madeleine, Gallagher, Charles G., Kalsheker, Noor, Aitken, Moira, Wiese, Dawn, Dunn, John, Smith, Paul, Pace, Rhonda, Londono, Douglas, Goddard, Katrina A. B., Knowles, Michael R., Drumm, Mitchell L.
Publicado em 2010

Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach

Por Abdulkadir, Mohamed, Londono, Douglas, Gordon, Derek, Fernandez, Thomas V., Brown, Lawrence W., Cheon, Keun-Ah, Coffey, Barbara J., Elzerman, Lonneke, Fremer, Carolin, Fründt, Odette, Garcia-Delgar, Blanca, Gilbert, Donald L., Grice, Dorothy E., Hedderly, Tammy, Heyman, Isobel, Hong, Hyun Ju, Huyser, Chaim, Ibanez-Gomez, Laura, Jakubovski, Ewgeni, Kim, Young Key, Kim, Young Shin, Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Leventhal, Bennett, Ludolph, Andrea G., Madruga-Garrido, Marcos, Maras, Athanasios, Mir, Pablo, Morer, Astrid, Müller-Vahl, Kirsten, Münchau, Alexander, Murphy, Tara L., Plessen, Kerstin J., Roessner, Veit, Shin, Eun-Young, Song, Dong-Ho, Song, Jungeun, Tübing, Jennifer, van den Ban, Els, Visscher, Frank, Wanderer, Sina, Woods, Martin, Zinner, Samuel H., King, Robert A., Tischfield, Jay A., Heiman, Gary A., Hoekstra, Pieter J., Dietrich, Andrea
Publicado no Eur Arch Psychiatry Clin Neurosci (2017)