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T. Gilliam · SciRah

Researcher profile · Semantic Scholar

T. Gilliam

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T. Gilliam — researcher profile on SciRah

h-index: 44
Works: 90
Citations: 12K

Most-cited papers

Large-Scale Copy Number Polymorphism in the Human Genome
J. Sebat, B. Lakshmi, J. Troge, Joan Alexander +17 more
2004Science2,603 citations
Semantic Scholar
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
R. Tanzi, K. Petrukhin, I. Chernov, J. Pellequer +19 more
1993Nature Genetics1,342 citations
Semantic Scholar
Cloning and genomic organization of beclin 1, a candidate tumor suppressor gene on chromosome 17q21.
V. M. Aita, Xiao-Huan Liang, V. Murty, David L. Pincus +5 more
1999Genomics856 citations Open access
Semantic Scholar
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.213.3
L. Brzustowicz, T. Lehner, L. Castilla, G. Penchaszadeh +12 more
1990Nature588 citations
Semantic Scholar
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
S. Kalachikov, O. Evgrafov, B. Ross, M. Winawer +14 more
2002Nature Genetics586 citations Open access
Semantic Scholar
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene
K. Petrukhin, S. Fischer, M. Pirastu, R. Tanzi +21 more
1993Nature Genetics495 citations
Semantic Scholar
Genetic homogeneity between acute and chronic forms of spinal muscular atrophy
T. Gilliam, L. Brzustowicz, L. Castilla, T. Lehner +10 more
1990Nature335 citations
Semantic Scholar
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
S. Christian, Camille W. Brune, Jyotsna Sudi, Ravinesh A. Kumar +13 more
2008Biological Psychiatry316 citations Open access
Semantic Scholar
A genomewide screen of 345 families for autism-susceptibility loci.
Amanda L. Yonan, M. Alarcón, R. Cheng, P. Magnusson +9 more
2003American Journal of Human Genetics289 citations Open access
Semantic Scholar
Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families.
M. Alarcón, R. Cantor, Jian-Jun Liu, T. Gilliam +1 more
2002American Journal of Human Genetics277 citations Open access
Semantic Scholar
Catechol-O-methyltransferase (COMT) genotypes and working memory: associations with differing cognitive operations.
G. Bruder, J. Keilp, Hai-Min Xu, M. Shikhman +3 more
2005Biological Psychiatry261 citations
Semantic Scholar
Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q.
M. McQueen, B. Devlin, S. Faraone, V. Nimgaonkar +49 more
2005American Journal of Human Genetics239 citations Open access
Semantic Scholar
Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation.
Olesia I. Buiakova, Jin Xu, S. Lutsenko, Scott Zeitlin +6 more
1999Human Molecular Genetics198 citations Open access
Semantic Scholar
Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q
K. ben Othmane, M. ben Hamida, M. Pericak-Vance, C. Ben Hamida +8 more
1992Nature Genetics186 citations
Semantic Scholar
LGI1 mutations in autosomal dominant partial epilepsy with auditory features
R. Ottman, M. Winawer, S. Kalachikov, C. Barker‐Cummings +3 more
2004Neurology183 citations Open access
Semantic Scholar
Linkage analysis of psychosis in bipolar pedigrees suggests novel putative loci for bipolar disorder and shared susceptibility with schizophrenia
N. Park, S. Juo, R. Cheng, Jian-Jun Liu +9 more
2004Molecular Psychiatry181 citations
Semantic Scholar
Linkage mapping of dopa–responsive dystonia (DRD) to chromosome 14q
T. Nygaard, K. Wilhelmsen, N. Risch, Deborah L. Brown +4 more
1993Nature Genetics174 citations
Semantic Scholar
Molecular triangulation: bridging linkage and molecular-network information for identifying candidate genes in Alzheimer's disease.
M. Krauthammer, C. Kaufmann, T. Gilliam, A. Rzhetsky
2004Proceedings of the National Academy of Sciences of the United States of America169 citations Open access
Semantic Scholar
Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorder
R. Cheng, S. Juo, J. Loth, J. Nee +11 more
2006Molecular Psychiatry159 citations Open access
Semantic Scholar
TULP1 mutation in two extended Dominican kindreds with autosomal recessive Retinitis pigmentosa
P. Banerjee, P. Kleyn, James A. Knowles, C. A. Lewis +8 more
1998Nature Genetics159 citations
Semantic Scholar
Evidence for a putative bipolar disorder locus on 2p13–16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21–24, 13q32, 14q21 and 17q11–12
Jian-Jun Liu, S. Juo, A. Dewan, A. Grunn +12 more
2003Molecular Psychiatry136 citations
Semantic Scholar
Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs
M. Alarcón, Amanda L. Yonan, T. Gilliam, R. Cantor +1 more
2005Molecular Psychiatry129 citations Open access
Semantic Scholar
Results of a genome-wide genetic screen for panic disorder.
James A. Knowles, A. Fyer, Veronica J. Vieland, M. Weissman +17 more
1998American journal of medical genetics126 citations Open access
Semantic Scholar
Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere.
T. Gilliam, R. Tanzi, J. Haines, T. Bonner +8 more
1987Cell124 citations
Semantic Scholar
Genomewide linkage analysis of celiac disease in Finnish families.
Jian-Jun Liu, S. Juo, P. Holopainen, J. Terwilliger +8 more
2002American Journal of Human Genetics120 citations Open access
Semantic Scholar
DNA markers for nervous system diseases.
J. Gusella, R. Tanzi, M. Anderson, W. Hobbs +6 more
1984Science116 citations
Semantic Scholar
Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy.
Ching H. Wang, Jin Xu, T. A. Carter, B. M. Ross +5 more
1996Human Molecular Genetics113 citations
Semantic Scholar
A DNA segment encoding two genes very tightly linked to Huntington's disease.
T. Gilliam, Maja Bucan, M. MacDonald, M. Zimmer +6 more
1987Science105 citations
Semantic Scholar
DRD2 C957T polymorphism interacts with the COMT Val158Met polymorphism in human working memory ability.
Hai-Min Xu, C. Kellendonk, E. Simpson, J. Keilp +4 more
2007Schizophrenia Research96 citations
Semantic Scholar
Panic Disorder is Associated with the Serotonin Transporter Gene (SLC6A4) But Not the Promoter Region (5-HTTLPR)
L. Strug, R. Suresh, A. Fyer, A. Talati +5 more
2008Molecular Psychiatry92 citations Open access
Semantic Scholar
Molecular and statistical approaches to the detection and correction of errors in genotype databases.
L. Brzustowicz, C. Mérette, Xiao-Xun Xie, L. Townsend +2 more
1993American Journal of Human Genetics90 citations
Semantic Scholar
Genetic mapping of “Lubag” (X‐linked dystonia‐parkinsonism) in a filipino kindred to the pericentromeric region of the X chromosome
K. C. Wilhelmsen, Daniel E. Weeks, Torbjoern G. Nygaard, C. Moskowitz +5 more
1991Annals of Neurology90 citations
Semantic Scholar
Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network.
I. Iossifov, T. Zheng, M. Baron, T. Gilliam +1 more
2008Genome Research74 citations Open access
Semantic Scholar
Four New Families with Autosomal Dominant Partial Epilepsy with Auditory Features: Clinical Description and Linkage to Chromosome 10q24
Melodie R. Winawer, F. M. Boneschi, C. Barker‐Cummings, Joseph H. Lee +6 more
2002Epilepsia74 citations Open access
Semantic Scholar
Phenotypic heterogeneity of spinal muscular atrophy mapping to chromosome 5q11.2‐13.3 (SMA 5q)
T. Munsat, L. Skerry, B. Korf, B. Pober +8 more
1990Neurology73 citations
Semantic Scholar
Bioinformatic analysis of autism positional candidate genes using biological databases and computational gene network prediction
Amanda L. Yonan, Abraham A. Palmer, K. Smith, I. Feldman +5 more
2003Genes, Brain and Behavior64 citations Open access
Semantic Scholar
Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration.
C. A. Lewis, I. Batlle, Karla G. R. Batlle, Poulabi Banerjee +8 more
1999Investigative Ophthalmology and Visual Science61 citations
Semantic Scholar
A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions.
T. A. Carter, C. Bonnemann, C.-H. Wang, S. Obici +8 more
1997Human Molecular Genetics61 citations Open access
Semantic Scholar
A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease gene.
M. MacDonald, M. Anderson, T. Gilliam, L. Tranebjærg +6 more
1987Genomics56 citations
Semantic Scholar
Screen for expanded FMR1 alleles in patients with essential tremor
Dolores Garcia-Arocena, E. Louis, F. Tassone, T. Gilliam +3 more
2004Movement Disorders54 citations
Semantic Scholar
Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene.
S. Selig, S. Bruno, Jeremiah M. Scharf, Chi-Guang Wang +3 more
1995Proceedings of the National Academy of Sciences of the United States of America54 citations Open access
Semantic Scholar
Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13.
L. Lien, Frederick M. Boyce, P. Kleyn, L. Brzustowicz +4 more
1991Proceedings of the National Academy of Sciences of the United States of America48 citations Open access
Semantic Scholar
Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia.
T. Gilliam, N. Freimer, Charles A. Kaufmann, P. Powchik +3 more
1989Genomics47 citations Open access
Semantic Scholar
Isolation of multiple genomic sequences coding for chicken myosin heavy chain protein.
J. Robbins, G. Freyer, D. Chisholm, T. Gilliam
1982Journal of Biological Chemistry45 citations Open access
Semantic Scholar
Physical mapping, linkage analysis of a putative schizophrenia locus on chromosome 5q.
Charles A. Kaufmann, L. DeLisi, T. Lehner, T. Gilliam
1989Schizophrenia bulletin44 citations Open access
Semantic Scholar
High resolution physical map of the region surrounding the spinal muscular atrophy gene.
T. Thompson, K. Morrison, P. Kleyn, U. Bengtsson +4 more
1993Human Molecular Genetics42 citations
Semantic Scholar
Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4.
W. Whaley, F. Michiels, M. MacDonald, Donna M. Romano +13 more
1988Nucleic Acids Research42 citations Open access
Semantic Scholar
Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22–q24
A. Martinez-Mir, A. Zlotogorski, D. Londono, D. Gordon +10 more
2003Journal of Medical Genetics41 citations Open access
Semantic Scholar
Association of extreme blood lipid profile phenotypic variation with 11 reverse cholesterol transport genes and 10 non-genetic cardiovascular disease risk factors.
A. Morabia, E. Cayanis, M. Costanza, B. Ross +4 more
2003Human Molecular Genetics39 citations Open access
Semantic Scholar
Perils of gene mapping with microsatellite markers.
James A. Knowles, Veronica J. Vieland, T. Gilliam
1992American Journal of Human Genetics35 citations
Semantic Scholar

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