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

Autor Zhang, Peisen, Sheng, Huitao, Morabia, Alfredo, Gilliam, T Conrad
Vydáno 2003

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

Autor Krauthammer, Michael, Kaufmann, Charles A., Gilliam, T. Conrad, Rzhetsky, Andrey
Vydáno 2004

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

Autor Iossifov, Ivan, Zheng, Tian, Baron, Miron, Gilliam, T. Conrad, Rzhetsky, Andrey
Vydáno 2008

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

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

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

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

Disease Gene Prioritization Using Network and Feature

Autor Xie, Bingqing, Agam, Gady, Balasubramanian, Sandhya, Xu, Jinbo, Gilliam, T. Conrad, Maltsev, Natalia, Börnigen, Daniela
Vydáno v J Comput Biol (2015)

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

Autor Xie, Bingqing, Laxman, Bharathi, Hashemifar, Somaye, Stern, Randi, Gilliam, T. Conrad, Maltsev, Natalia, White, Steven R.
Vydáno v 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

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

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

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

Evidence for Sex-Specific Risk Alleles in Autism Spectrum Disorder

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

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

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

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

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

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

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

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

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

Lynx: a database and knowledge extraction engine for integrative medicine

Autor 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
Vydáno 2014

Genomewide Linkage Analysis of Celiac Disease in Finnish Families

Autor 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
Vydáno 2002

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

Autor 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
Vydáno 2002

A Genomewide Screen for Autism Susceptibility Loci

Autor 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
Vydáno 2001

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

Autor 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
Vydáno v Nucleic Acids Res (2016)

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

Autor 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. 
Vydáno 2007