Optimal Step Length EM Algorithm (OSLEM) for the estimation of haplotype frequency and its application in lipoprotein lipase genotyping

by Zhang, Peisen, Sheng, Huitao, Morabia, Alfredo, Gilliam, T Conrad
Published 2003

Molecular triangulation: Bridging linkage and molecular-network information for identifying candidate genes in Alzheimer's disease

by Krauthammer, Michael, Kaufmann, Charles A., Gilliam, T. Conrad, Rzhetsky, Andrey
Published 2004

Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network

by Iossifov, Ivan, Zheng, Tian, Baron, Miron, Gilliam, T. Conrad, Rzhetsky, Andrey
Published 2008

Evidence for a Language Quantitative Trait Locus on Chromosome 7q in Multiplex Autism Families

by Alarcón, Maricela, Cantor, Rita M., Liu, Jianjun, Gilliam, T. Conrad, Geschwind, Daniel H.
Published 2002

Altered Hippocampal Transcript Profile Accompanies an Age-Related Spatial Memory Deficit in Mice

by Verbitsky, Miguel, Yonan, Amanda L., Malleret, Gaël, Kandel, Eric R., Gilliam, T. Conrad, Pavlidis, Paul
Published 2004

Disease Gene Prioritization Using Network and Feature

by Xie, Bingqing, Agam, Gady, Balasubramanian, Sandhya, Xu, Jinbo, Gilliam, T. Conrad, Maltsev, Natalia, Börnigen, Daniela
Published in J Comput Biol (2015)

Chemokine expression in the early response to injury in human airway epithelial cells

by Xie, Bingqing, Laxman, Bharathi, Hashemifar, Somaye, Stern, Randi, Gilliam, T. Conrad, Maltsev, Natalia, White, Steven R.
Published in PLoS One (2018)

Rapid Selection Response for Contextual Fear Conditioning in a Cross Between C57BL/6J and A/J: Behavioral, QTL and Gene Expression Analysis

by Ponder, Christine A., Huded, Chetan P., Munoz, Michaelanne B., Gulden, Forrest O., Gilliam, T. Conrad, Palmer, Abraham A.
Published in Behav Genet (2008)

Deletion Mapping of DNA Markers to a Region of Chromosome 5 That Cosegregates with Schizophrenia

by Gilliam, T. Conrad, Freimer, Nelson B., Kaufmann, Charles A., Powchik, Peter P., Bassett, Anne S., Bengtsson, Ulla, Wasmuth, John J.
Published 1989

Evidence for Sex-Specific Risk Alleles in Autism Spectrum Disorder

by Stone, Jennifer L., Merriman, Barry, Cantor, Rita M., Yonan, Amanda L., Gilliam, T. Conrad, Geschwind, Daniel H., Nelson, Stanley F.
Published 2004

Genetic and Physical Mapping of the Progressive Epilepsy with Mental Retardation (EPMR) Locus on Chromosome 8p

by Ranta, Susanna, Lehesjoki, Anna-Elina, Hirvasniemi, Aune, Weissenbach, Jean, Ross, Barbara, Leal, Suzanne M., de la Chapelle, Albert, Gilliam, T. Conrad
Published in Genome Res (1996)

Lynx web services for annotations and systems analysis of multi-gene disorders

by Sulakhe, Dinanath, Taylor, Andrew, Balasubramanian, Sandhya, Feng, Bo, Xie, Bingqing, Börnigen, Daniela, Dave, Utpal J., Foster, Ian T., Gilliam, T. Conrad, Maltsev, Natalia
Published 2014

Exploring the functional impact of alternative splicing on human protein isoforms using available annotation sources

by Sulakhe, Dinanath, D’Souza, Mark, Wang, Sheng, Balasubramanian, Sandhya, Athri, Prashanth, Xie, Bingqing, Canzar, Stefan, Agam, Gady, Gilliam, T Conrad, Maltsev, Natalia
Published in Brief Bioinform (2019)

Panic Disorder is Associated with the Serotonin Transporter Gene (SLC6A4) But Not the Promoter Region (5-HTTLPR)

by Strug, Lisa J., Suresh, Rathi, Fyer, Abby, Talati, Ardesheer, Adams, Philip B., Li, Weili, Hodge, Susan E., Gilliam, T. Conrad, Weissman, Myrna M.
Published 2008

Lynx: a database and knowledge extraction engine for integrative medicine

by Sulakhe, Dinanath, Balasubramanian, Sandhya, Xie, Bingqing, Feng, Bo, Taylor, Andrew, Wang, Sheng, Berrocal, Eduardo, Dave, Utpal, Xu, Jinbo, Börnigen, Daniela, Gilliam, T. Conrad, Maltsev, Natalia
Published 2014

Genomewide Linkage Analysis of Celiac Disease in Finnish Families

by Liu, Jianjun, Juo, Suh-Hang, Holopainen, Päivi, Terwilliger, Joseph, Tong, Xiaomei, Grunn, Adina, Brito, Miguel, Green, Peter, Mustalahti, Kirsi, Mäki, Markku, Gilliam, T. Conrad, Partanen, Jukka
Published 2002

Four New Families with Autosomal Dominant Partial Epilepsy with Auditory Features: Clinical Description and Linkage to Chromosome 10q24

by Winawer, Melodie R., Boneschi, Filippo Martinelli, Barker-Cummings, Christie, Lee, Joseph H., Liu, Jianjun, Mekios, Constantine, Gilliam, T. Conrad, Pedley, Timothy A., Hauser, W. Allen, Ottman, Ruth
Published 2002

A Genomewide Screen for Autism Susceptibility Loci

by Liu, Jianjun, Nyholt, Dale R., Magnussen, Patrick, Parano, Enrico, Pavone, Piero, Geschwind, Daniel, Lord, Catherine, Iversen, Portia, Hoh, Josephine, Autism Genetic Resource Exchange Consortium, the, Ott, Jurg, Gilliam, T. Conrad
Published 2001

Lynx: a knowledge base and an analytical workbench for integrative medicine

by Sulakhe, Dinanath, Xie, Bingqing, Taylor, Andrew, D'Souza, Mark, Balasubramanian, Sandhya, Hashemifar, Somaye, White, Steven, Dave, Utpal J., Agam, Gady, Xu, Jinbo, Wang, Sheng, Gilliam, T. Conrad, Maltsev, Natalia
Published in Nucleic Acids Res (2016)

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

by 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. 
Published 2007