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

gan Zhang, Peisen, Sheng, Huitao, Morabia, Alfredo, Gilliam, T Conrad
Cyhoeddwyd 2003

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

gan Krauthammer, Michael, Kaufmann, Charles A., Gilliam, T. Conrad, Rzhetsky, Andrey
Cyhoeddwyd 2004

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

gan Iossifov, Ivan, Zheng, Tian, Baron, Miron, Gilliam, T. Conrad, Rzhetsky, Andrey
Cyhoeddwyd 2008

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

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

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

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

Disease Gene Prioritization Using Network and Feature

gan Xie, Bingqing, Agam, Gady, Balasubramanian, Sandhya, Xu, Jinbo, Gilliam, T. Conrad, Maltsev, Natalia, Börnigen, Daniela
Cyhoeddwyd yn J Comput Biol (2015)

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

gan Xie, Bingqing, Laxman, Bharathi, Hashemifar, Somaye, Stern, Randi, Gilliam, T. Conrad, Maltsev, Natalia, White, Steven R.
Cyhoeddwyd yn 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

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

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

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

Evidence for Sex-Specific Risk Alleles in Autism Spectrum Disorder

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

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

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

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

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

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

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

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

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

Lynx: a database and knowledge extraction engine for integrative medicine

gan 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
Cyhoeddwyd 2014

Genomewide Linkage Analysis of Celiac Disease in Finnish Families

gan 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
Cyhoeddwyd 2002

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

gan 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
Cyhoeddwyd 2002

A Genomewide Screen for Autism Susceptibility Loci

gan 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
Cyhoeddwyd 2001

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

gan 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
Cyhoeddwyd yn Nucleic Acids Res (2016)

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

gan 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. 
Cyhoeddwyd 2007