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

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

Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities

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

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

Tekijä Gordon, Derek, Londono, Douglas, Patel, Payal, Kim, Wonkuk, Finch, Stephen J., Heiman, Gary A.
Julkaisussa 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

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

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

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

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

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

Density-based clustering in haplotype analysis for association mapping

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

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

Tekijä 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
Julkaistu 2012

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

Tekijä 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. 
Julkaistu 2007

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

Tekijä 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.
Julkaisussa Nat Commun (2018)

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

Tekijä 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.
Julkaisussa Nat Commun (2015)

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

Tekijä 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.
Julkaistu 2011

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

Tekijä 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.
Julkaistu 2014

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

Tekijä 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.
Julkaistu 2010

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

Tekijä 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
Julkaisussa Eur Arch Psychiatry Clin Neurosci (2017)