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

le Zhang, Peisen, Sheng, Huitao, Morabia, Alfredo, Gilliam, T Conrad
Foilsithe 2003

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

le Krauthammer, Michael, Kaufmann, Charles A., Gilliam, T. Conrad, Rzhetsky, Andrey
Foilsithe 2004

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

le Iossifov, Ivan, Zheng, Tian, Baron, Miron, Gilliam, T. Conrad, Rzhetsky, Andrey
Foilsithe 2008

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

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

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

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

Disease Gene Prioritization Using Network and Feature

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

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

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

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

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

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

Evidence for Sex-Specific Risk Alleles in Autism Spectrum Disorder

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

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

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

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

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

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

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

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

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

Lynx: a database and knowledge extraction engine for integrative medicine

le 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
Foilsithe 2014

Genomewide Linkage Analysis of Celiac Disease in Finnish Families

le 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
Foilsithe 2002

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

le 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
Foilsithe 2002

A Genomewide Screen for Autism Susceptibility Loci

le 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
Foilsithe 2001

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

le 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
Foilsithe in Nucleic Acids Res (2016)

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

le 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. 
Foilsithe 2007