Recurrent 16p11.2 microdeletions in autism von Kumar, Ravinesh A., KaraMohamed, Samer, Sudi, Jyotsna, Conrad, Donald F., Brune, Camille, Badner, Judith A., Gilliam, T. Conrad, Nowak, Norma J., Cook, Edwin H., Dobyns, William B., Christian, Susan L.

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Large-Scale Copy Number Polymorphism in the Human Genome von Sebat, Jonathan, Lakshmi, B., Troge, Jennifer, Alexander, Joan, Young, Janet, Lundin, Pär, Månér, Susanne, Massa, Hillary, Walker, Megan, Chi, Maoyen, Navin, Nicholas, Lucito, Robert, Healy, John, Hicks, James, Ye, Kenny, Reiner, Andrew, Gilliam, T. Conrad, Trask, Barbara, Patterson, Nick, Zetterberg, Anders, Wigler, Michael

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Exploring the functional impact of alternative splicing on human protein isoforms using available annotation sources von Sulakhe, Dinanath, D’Souza, Mark, Wang, Sheng, Balasubramanian, Sandhya, Athri, Prashanth, Xie, Bingqing, Canzar, Stefan, Agam, Gady, Gilliam, T Conrad, Maltsev, Natalia

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Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder von Christian, Susan L, Brune, Camille W, Sudi, Jyotsna, Kumar, Ravinesh A, Liu, Shaung, Karamohamed, Samer, Badner, Judith A, Matsui, Seiichi, Conroy, Jeffrey, McQuaid, Devin, Gergel, James, Hatchwell, Eli, Gilliam, T. Conrad, Gershon, Elliot S, Nowak, Norma J, Dobyns, William B, Cook, Edwin H

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Chemokine expression in the early response to injury in human airway epithelial cells von Xie, Bingqing, Laxman, Bharathi, Hashemifar, Somaye, Stern, Randi, Gilliam, T Conrad, Maltsev, Natalia, White, Steven R

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Consequences of Copper Accumulation in the Livers of the Atp7b −/− (Wilson Disease Gene) Knockout Mice von Huster, Dominik, Finegold, Milton J., Morgan, Clinton T., Burkhead, Jason L., Nixon, Randal, Vanderwerf, Scott M., Gilliam, Conrad T., Lutsenko, Svetlana

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Strategic Integration of Multiple Bioinformatics Resources for System Level Analysis of Biological Networks von D’Souza, Mark, Sulakhe, Dinanath, Wang, Sheng, Xie, Bing, Hashemifar, Somaye, Taylor, Andrew, Dubchak, Inna, Conrad Gilliam, T., Maltsev, Natalia

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Molecular Triangulation: Bridging Linkage and Molecular-Network Information for Identifying Candidate Genes in Alzheimer's Disease von Krauthammer, Michael, Kaufmann, Charles A., Gilliam, T. Conrad, Rzhetsky, Andrey, Wigler, Michael H.

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Evidence for Sex-Specific Risk Alleles in Autism Spectrum Disorder von Stone, Jennifer L., Merriman, Barry, Cantor, Rita M., Yonan, Amanda L., Gilliam, T. Conrad, Geschwind, Daniel H., Nelson, Stanley F.

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

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Unique somatic variants in DNA from urine exosomes of individuals with bladder cancer von Zhou, Xunian, Kurywchak, Paul, Wolf-Dennen, Kerri, Che, Sara P.Y., Sulakhe, Dinanath, D’Souza, Mark, Xie, Bingqing, Maltsev, Natalia, Gilliam, T. Conrad, Wu, Chia-Chin, McAndrews, Kathleen M., LeBleu, Valerie S., McConkey, David J., Volpert, Olga V., Pretzsch, Shanna M., Czerniak, Bogdan A., Dinney, Colin P., Kalluri, Raghu

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Altered Hippocampal Transcript Profile Accompanies an Age-Related Spatial Memory Deficit in Mice von Verbitsky, Miguel, Yonan, Amanda L, Malleret, Gael, Kandel, Eric R, Gilliam, T. Conrad, Pavlidis, Paul

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Evidence for a Language Quantitative Trait Locus on Chromosome 7q in Multiplex Autism Families von Alarcón, Maricela, Cantor, Rita M., Liu, Jianjun, Gilliam, T. Conrad, Geschwind, Daniel H.

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Molecular Interaction Network Approach (MINA) identifies association of novel candidate disease genes von Kara, Sam, Hanna, Alaa, Pirela-Morillo, Gerardo A., Gilliam, Conrad T., Wilson, George D.

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An integrative computational approach for prioritization of genomic variants von Dubchak, Inna, Balasubramanian, Sandhya, Wang, Sheng, Cem, Meydan, Meyden, Cem, Sulakhe, Dinanath, Poliakov, Alexander, Börnigen, Daniela, Xie, Bingqing, Taylor, Andrew, Ma, Jianzhu, Paciorkowski, Alex R, Mirzaa, Ghayda M, Dave, Paul, Agam, Gady, Xu, Jinbo, Al-Gazali, Lihadh, Mason, Christopher E, Ross, M Elizabeth, Maltsev, Natalia, Gilliam, T Conrad

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Selection for contextual fear conditioning affects anxiety‐like behaviors and gene expression von Ponder, C. A., Kliethermes, C. L., Drew, M. R., Muller, J., Das, K., Risbrough, V. B., Crabbe, J. C., Gilliam, T. Conrad, Palmer, A. A.

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Strong Association of De Novo Copy Number Mutations with Autism von Sebat, Jonathan, Lakshmi, B, Malhotra, Dheeraj, Troge, Jennifer, Lese-Martin, Christa, Walsh, Tom, Yamrom, Boris, Yoon, Seungtai, Krasnitz, Alex, Kendall, Jude, Leotta, Anthony, Pai, Deepa, Zhang, Ray, Lee, Yoon-Ha, Hicks, James, Spence, Sarah J, Lee, Annette T, Puura, Kaija, Lehtimäki, Terho, Ledbetter, David, Gregersen, Peter K, Bregman, Joel, Sutcliffe, James S, Jobanputra, Vaidehi, Chung, Wendy, Warburton, Dorothy, King, Mary-Claire, Skuse, David, Geschwind, Daniel H, Gilliam, T. Conrad, Ye, Kenny, Wigler, Michael

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A p53-regulated apoptotic gene signature predicts treatment response and outcome in pediatric acute lymphoblastic leukemia von Bainer, Russell O, Trendowski, Matthew R, Cheng, Cheng, Pei, Deqing, Yang, Wenjian, Paugh, Steven W, Goss, Kathleen H, Skol, Andrew D, Pavlidis, Paul, Pui, Ching-Hon, Gilliam, T Conrad, Evans, William E, Onel, Kenan

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Genetic architecture of fear conditioning in chromosome substitution strains: relationship to measures of innate (unlearned) anxiety-like behavior von Ponder, Christine A, Munoz, Michaelanne, Gilliam, T. Conrad, Palmer, Abraham A

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Identification of novel susceptibility genes associated with seven autoimmune disorders using whole genome molecular interaction networks von Kara, Sam, Pirela-Morillo, Gerardo A., Gilliam, Conrad T., Wilson, George D.

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