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

di Londono, Douglas, Buyske, Steven, Finch, Stephen J, Sharma, Swarkar, Wise, Carol A, Gordon, Derek
Pubblicazione 2012

Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities

di Musolf, Anthony, Nato, Alejandro Q, Londono, Douglas, Zhou, Lisheng, Matise, Tara C, Gordon, Derek
Pubblicazione 2014

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

di Gordon, Derek, Londono, Douglas, Patel, Payal, Kim, Wonkuk, Finch, Stephen J., Heiman, Gary A.
Pubblicato in 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

di Briant, Judith A., Nielsen, David A., Proudnikov, Dmitri, Londono, Douglas, Ho, Ann, Ott, Jurg, Kreek, Mary Jeanne
Pubblicazione 2010

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

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

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

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

Density-based clustering in haplotype analysis for association mapping

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

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

di 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
Pubblicazione 2012

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

di 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. 
Pubblicazione 2007

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

di 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.
Pubblicato in Nat Commun (2018)

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

di 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.
Pubblicato in Nat Commun (2015)

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

di 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.
Pubblicazione 2011

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

di 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.
Pubblicazione 2014

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

di 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.
Pubblicazione 2010

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

di 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
Pubblicato in Eur Arch Psychiatry Clin Neurosci (2017)