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

di Zhang, Peisen, Sheng, Huitao, Morabia, Alfredo, Gilliam, T Conrad
Pubblicazione 2003

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

di Krauthammer, Michael, Kaufmann, Charles A., Gilliam, T. Conrad, Rzhetsky, Andrey
Pubblicazione 2004

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

di Iossifov, Ivan, Zheng, Tian, Baron, Miron, Gilliam, T. Conrad, Rzhetsky, Andrey
Pubblicazione 2008

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

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

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

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

Disease Gene Prioritization Using Network and Feature

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

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

di Xie, Bingqing, Laxman, Bharathi, Hashemifar, Somaye, Stern, Randi, Gilliam, T. Conrad, Maltsev, Natalia, White, Steven R.
Pubblicato 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

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

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

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

Evidence for Sex-Specific Risk Alleles in Autism Spectrum Disorder

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

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

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

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

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

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

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

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

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

Lynx: a database and knowledge extraction engine for integrative medicine

di 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
Pubblicazione 2014

Genomewide Linkage Analysis of Celiac Disease in Finnish Families

di 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
Pubblicazione 2002

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

di 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
Pubblicazione 2002

A Genomewide Screen for Autism Susceptibility Loci

di 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
Pubblicazione 2001

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

di 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
Pubblicato in Nucleic Acids Res (2016)

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