Gilliam, T.Conrad: search on Z-Library

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1

Inducible Enhancement of Memory Storage and Synaptic Plasticity in Transgenic Mice Expressing an Inhibitor of ATF4 (CREB-2) and C/EBP Proteins

Amy Chen, Isabel A Muzzio, Gaël Malleret, Dusan Bartsch, Miguel Verbitsky, Paul Pavlidis, Amanda L Yonan, Svetlana Vronskaya, Michael B Grody, Ivan Cepeda, T.Conrad Gilliam, Eric R Kandel

Journal:

Year:

2003

Language:

english

File:

PDF, 638 KB

english, 2003

2

DRD2 C957T polymorphism interacts with the COMT Val158Met polymorphism in human working memory ability

Haiyan Xu, Christoph B. Kellendonk, Eleanor H. Simpson, John G. Keilp, Gerard E. Bruder, H. Jonathan Polan, Eric R. Kandel, T. Conrad Gilliam

Journal:

Schizophrenia Research

Year:

2007

Language:

english

File:

PDF, 151 KB

english, 2007

3

EB Simplex Superficialis Resulting from a Mutation in the Type VII Collagen Gene

Martinez-Mir, Amalia, Liu, Jianjun, Gordon, Derek, Weiner, Madeline S., Ahmad, Wasim, Fine, Jo-David, Ott, Jurg, Conrad Gilliam, T., Christiano, Angela M.

Journal:

The Journal of Investigative Dermatology

Year:

2002

Language:

english

File:

PDF, 122 KB

english, 2002

4

A Microsatellite Genetic Linkage Map of Human Chromosome 13

Konstantin E. Petrukhin, Marcy C. Speer, Eftihia Cayanis, Maria de Fátima Bonaldo, Umadevi Tantravahi, Marcelo Bento Soares, Stuart G. Fischer, Dorothy Warburton, T.Conrad Gilliam, Jurg Ott

Journal:

Year:

1993

File:

PDF, 572 KB

1993

5

Bipolar disorder and linkage to Xq28

Baron, Miron, Straub, Richard E., Lehner, Thomas, Endicott, Jean, Ott, Jurg, Gilliam, T. Conrad, Lerer, Bernard

Journal:

Nature Genetics

Year:

1994

File:

PDF, 127 KB

1994

6

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

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, Ma

Journal:

Nucleic Acids Research

Year:

2015

Language:

english

File:

PDF, 873 KB

english, 2015

7

Dinucleotide repeat polymorphism at the D1S182 locus

Petrukhin, Konstantin E., Gilliam, T.Conrad

Journal:

Human Molecular Genetics

Year:

1992

Language:

english

File:

PDF, 73 KB

english, 1992

8

A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease gene

MacDonald, Marcy E., Anderson, Mary Anne, Gilliam, T. Conrad, Tranebjaerg, Lisbeth, Carpenter, Nancy J., Magenis, Ellen, Hayden, Michael R., Healey, Steven T., Bonner, Tom I., Gusella, James F.

Journal:

Year:

1987

Language:

english

File:

PDF, 767 KB

english, 1987

9

Chromosome Jumping from D4S10 (G8) toward the Huntington Disease Gene

Julia E. Richards, T. Conrad Gilliam, Jeffery L. Cole, Mitchell L. Drumm, John J. Wasmuth, James F. Gusella and Francis S. Collins

Journal:

Proceedings of the National Academy of Sciences

Year:

1988

Language:

english

File:

PDF, 1.09 MB

english, 1988

10

Gene expression differences in mice divergently selected for methamphetamine sensitivity

Abraham A. Palmer, Miguel Verbitsky, Rathi Suresh, Helen M. Kamens, Cheryl L. Reed, Na Li, Sue Burkhart–Kasch, Carrie S. McKinnon, John K. Belknap, T. Conrad Gilliam, Tamara J. Phillips

Journal:

Mammalian Genome

Year:

2005

Language:

english

File:

PDF, 194 KB

english, 2005

11

Innovation: Digital genotyping using molecular affinity and mass spectrometry

Kim, Sobin, Ruparel, Hameer D., Gilliam, T. Conrad, Ju, Jingyue

Journal:

Nature Reviews Genetics

Year:

2003

Language:

english

File:

PDF, 273 KB

english, 2003

12

Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4

Whaley, William L., Michiels, Frank, MacDonald, Marcy E., Romano, Donna, Zimmer, Michael, Smith, Barbara, Leavitt, Julie, Bucan, Maja, Haines, Jonathan L., Gilliam, T. Conrad, Zehetner, Gunther, Smith

Journal:

Nucleic Acids Research

Year:

1988

Language:

english

File:

PDF, 1.05 MB

english, 1988

13

Is the Spinal Muscular Atrophy gene found?

Gilliam, T. Conrad

Journal:

Nature Medicine

Year:

1995

File:

PDF, 721 KB

1995

14

High resolution physical map of the region surrounding the spinal muscular atrophy gene

Thompson, Terrl G., Morrison, Karen E., Kleyn, Patrick, Bengtsson, Ulla, Gilliam, T.Conrad, Davies, Kay E., Wasmuth, John J., McPherson, John D.

Journal:

Human Molecular Genetics

Year:

1993

Language:

english

File:

PDF, 2.84 MB

english, 1993

15

Refinement of the Spinal Muscular Atrophy Locus to the Interval between D5S435 and MAP1B

Vera M. Soares, Linda M. Brzustowicz, Patrick W. Kleyn, James A. Knowles, David A. Palmer, Susha Asokan, Graciela K. Penchaszadeh, Theodore L. Munsat, T.Conrad Gilliam

Journal:

Year:

1993

File:

PDF, 452 KB

1993

16

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

Amalia Martinez-Mir, Abraham Zlotogorski, Derek Gordon, Lynn Petukhova, Jianhong Mo, T. Conrad Gilliam, Douglas Londono, Chad Haynes, Jurg Ott, Maria Hordinsky, Krassimira Nanova, David Norris, Vera P

Journal:

The American Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 7.06 MB

english, 2007

17

Two forms of Wilson disease protein produced by alternative splicing are localized in distinct cellular compartments

YANG, Xiao-Li, MIURA, Naoyuki, KAWARADA, Yoshihiko, TERADA, Kunihiko, PETRUKHIN, Konstantin, GILLIAM, T. Conrad, SUGIYAMA, Toshihiro

Journal:

Biochemical Journal

Year:

1997

Language:

english

File:

PDF, 354 KB

english, 1997

18

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

Sulakhe, Dinanath, D’Souza, Mark, Wang, Sheng, Balasubramanian, Sandhya, Athri, Prashanth, Xie, Bingqing, Canzar, Stefan, Agam, Gady, Gilliam, T Conrad, Maltsev, Natalia

Journal:

Briefings in Bioinformatics

Year:

2018

Language:

english

File:

PDF, 1.45 MB

english, 2018

19

Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q

Ben Othmane, Kamel, Ben Hamida, Mongi, Pericak-Vance, Margaret A., Ben Hamida, Christiane, Blel, Samir, Carter, Susan C., Bowcock, Anne M., Petruhkin, Konstantin, Conrad Gilliam, T., Roses, Allen D.

Journal:

Nature Genetics

Year:

1992

File:

PDF, 301 KB

1992

20

Linkage mapping of dopa–responsive dystonia (DRD) to chromosome 14q

Nygaard, Torbjoern G., Wilhelmsen, Kirk C., Risch, Neil J., Brown, Deborah L., Trugman, Joel M., Conrad Gilliam, T., Fahn, Stanley, Weeks, Daniel E.

Journal:

Nature Genetics

Year:

1993

File:

PDF, 541 KB

1993

21

Preliminary linkage analysis of schizophrenia in Canadian pedigrees to a candidate region on chromosome 5

Bassett, AnneS., Sandkuyl, Lodewijk, Lehner, Thomas, Powchik, Peter, Gilliam, T.Conrad, Kaufman, CharlesA.

Journal:

Schizophrenia Research

Year:

1989

Language:

english

File:

PDF, 82 KB

english, 1989

22

Hardy???Weinberg disequilibrium identified genotyping error of the serotonin transporter (SLC6A4) promoter polymorphism

Yonan, Amanda L., Palmer, Abraham A., Gilliam, Thomas Conrad

Journal:

Psychiatric Genetics

Year:

2006

Language:

english

File:

PDF, 76 KB

english, 2006

23

Identification of novel susceptibility genes associated with seven autoimmune disorders using whole genome molecular interaction networks

Kara, Sam, Pirela-Morillo, Gerardo A., Gilliam, Conrad T., Wilson, George D.

Journal:

Journal of Autoimmunity

Year:

2018

Language:

english

File:

PDF, 1.76 MB

english, 2018

24

Genetic architecture of fear conditioning in chromosome substitution strains: relationship to measures of innate (unlearned) anxiety-like behavior

Christine A. Ponder, Michaelanne Munoz, T. Conrad Gilliam, Abraham A. Palmer

Journal:

Mammalian Genome

Year:

2007

Language:

english

File:

PDF, 248 KB

english, 2007

25

[Advances in Experimental Medicine and Biology] Systems Analysis of Human Multigene Disorders Volume 799 || Characterizing Multi-omic Data in Systems Biology

Maltsev, Natalia, Rzhetsky, Andrey, Gilliam, T. Conrad

Year:

2014

Language:

english

File:

PDF, 489 KB

english, 2014

26

Dinucleotide repeat polymorphism at the D4S251 locus

Petrukhin, Konstantin E., Modyanov, Nikolai N., Gilliam, T. Conrad

Journal:

Human Molecular Genetics

Year:

1992

Language:

english

File:

PDF, 94 KB

english, 1992

27

Isolation of polymorphic DNA fragments from human chromosome 4

Gilliam, T.Conrad, Healey, Steven T., MacDonald, Marcy E., Stewan, Gordon D., Wasmuth, John J., Tanzi, Rudolph E., Roy, Jerry C., Gusella, James F.

Journal:

Nucleic Acids Research

Year:

1987

Language:

english

File:

PDF, 1.60 MB

english, 1987

28

Rapid Selection Response for Contextual Fear Conditioning in a Cross Between C57BL/6J and A/J: Behavioral, QTL and Gene Expression Analysis

Christine A. Ponder, Chetan P. Huded, Michaelanne B. Munoz, Forrest O. Gulden, T. Conrad Gilliam, Abraham A. Palmer

Journal:

Behavior Genetics

Year:

2008

Language:

english

File:

PDF, 400 KB

english, 2008

29

Genomewide Linkage Analysis of Celiac Disease in Finnish Families

Jianjun Liu, Suh-Hang Juo, Päivi Holopainen, Joseph Terwilliger, Xiaomei Tong, Adina Grunn, Miguel Brito, Peter Green, Kirsi Mustalahti, Markku Mäki, T. Conrad Gilliam, Jukka Partanen

Journal:

The American Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 84 KB

english, 2002

30

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

Peisen Zhang, Huitao Sheng, Alfredo Morabia, T Conrad Gilliam

Journal:

BMC Bioinformatics

Year:

2003

Language:

english

File:

PDF, 215 KB

english, 2003

31

Heparin and Its Non-Anticoagulant Analogues Inhibit Human Keratinocyte Growth Without Inducing Differentiation.

Pillai, Sreekumar, Gilliam, Lisa, Conrad, H. Edward, Holleran, Walter M.

Journal:

The Journal of Investigative Dermatology

Year:

1994

Language:

english

File:

PDF, 5.05 MB

english, 1994

32

Genetic disorders of copper metabolism

Petrukhin, Konstantin, Gilliam, T. Conrad

Journal:

Current Opinion in Pediatrics

Year:

1994

File:

PDF, 368 KB

1994

33

Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q

Haiyan Xu, Rong Cheng, Suh-Hang Juo, Jianjun Liu, Jo Ellen Loth, Jean Endicott, Conrad Gilliam, Miron Baron

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2011

Language:

english

File:

PDF, 182 KB

english, 2011

34

Arm tremor secondary to Wilson's disease

Dr. Steven Frucht, Dexter Sun, Nicholas Schiff, David Eidelberg, T. Conrad Gilliam

Journal:

Movement Disorders

Year:

1998

Language:

english

File:

PDF, 639 KB

english, 1998

35

A genetic linkage map of the chromosome 4 short arm

Patricia A. Locke, Marcy E. MacDonald, Jayalakshmi Srinidhi, T. Conrad Gilliam, Rudolph E. Tanzi, P. Michael Conneally, Nancy S. Wexler, Jonathan L. Haines, James F. Gusella

Journal:

Somatic Cell and Molecular Genetics

Year:

1993

Language:

english

File:

PDF, 649 KB

english, 1993

36

Evidence for Sex-Specific Risk Alleles in Autism Spectrum Disorder

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

Journal:

The American Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 257 KB

english, 2004

37

Selection for contextual fear conditioning affects anxiety-like behaviors and gene expression

C. A. Ponder, C. L. Kliethermes, M. R. Drew, J. Muller, K. Das, V. B. Risbrough, J. C. Crabbe, T. Conrad Gilliam, A. A. Palmer

Journal:

Genes, Brain and Behavior

Year:

2007

Language:

english

File:

PDF, 493 KB

english, 2007

38

A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22

Jianjun Liu, Suh Hang Juo, Joseph D. Terwilliger, Adina Grunn, Xiaomei Tong, Miguel Brito, Jo Ellen Loth, Kyra Kanyas, Bernard Lerer, Jean Endicott, Graciela Penchaszadeh, Dr. T. Conrad Gilliam, Dr. M

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 76 KB

english, 2001

39

Homozygosity and Physical Mapping of the Autosomal Recessive Retinitis Pigmentosa Locus (RP14) on Chromosome 6p21.3

Poulabi Banerjee, Charles A. Lewis, Patrick W. Kleyn, Yin Y. Shugart, Barbara M. Ross, Graciela K. Penchaszadeh, Jurg Ott, Samuel G. Jacobson, T.Conrad Gilliam, James A. Knowles

Journal:

Year:

1998

Language:

english

File:

PDF, 179 KB

english, 1998

40

[ACM Press the International Conference - Wshington DC, USA (2013.09.22-2013.09.25)] Proceedings of the International Conference on Bioinformatics, Computational Biology and Biomedical Informatics - BCB'13 - Conditional Random Field for Candidate Gene Prioritization

Xie, Bingqing, Agam, Gady, Maltsev, Natalia, Gilliam, Conrad

Year:

2007

Language:

english

File:

PDF, 124 KB

english, 2007

41

Cloning and Genomic Organization of Beclin 1, a Candidate Tumor Suppressor Gene on Chromosome 17q21

Vincent M. Aita, Xiao Huan Liang, V.V.V.S. Murty, David L. Pincus, Weiping Yu, Eftihia Cayanis, Sergei Kalachikov, T.Conrad Gilliam, Beth Levine

Journal:

Year:

1999

Language:

english

File:

PDF, 188 KB

english, 1999

42

[Advances in Experimental Medicine and Biology] Systems Analysis of Human Multigene Disorders Volume 799 ||

Maltsev, Natalia, Rzhetsky, Andrey, Gilliam, T. Conrad

Year:

2014

Language:

english

File:

PDF, 3.03 MB

english, 2014

43

Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia

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

Journal:

Year:

1989

Language:

english

File:

PDF, 1.51 MB

english, 1989

44

[Advances in Experimental Medicine and Biology] Systems Analysis of Human Multigene Disorders Volume 799 || A Personalized Treatment for Lung Cancer: Molecular Pathways, Targeted Therapies, and Genomic Characterization

Maltsev, Natalia, Rzhetsky, Andrey, Gilliam, T. Conrad

Year:

2014

Language:

english

File:

PDF, 300 KB

english, 2014

45

Mapping of Human Microtubule-Associated Protein 1B in Proximity to the Spinal Muscular Atrophy Locus at 5q13

Lyndon L. Lien, Frederick M. Boyce, Patrick Kleyn, Linda M. Brzustowicz, Joan Menninger, David C. Ward, T. Conrad Gilliam and Louis M. Kunkel

Journal:

Proceedings of the National Academy of Sciences

Year:

1991

Language:

english

File:

PDF, 971 KB

english, 1991

46

Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues

Dr. Ching H. Wang, Todd A. Carter, Kamna Das, Jin Xu, Barbara M. Ross, Graciela K. Penchaszadeh, T. Conrad Gilliam

Journal:

Annals of Neurology

Year:

1997

Language:

english

File:

PDF, 1.04 MB

english, 1997

47

Catechol-O-Methyltransferase (COMT) Genotypes and Working Memory: Associations with Differing Cognitive Operations

Gerard E. Bruder, John G. Keilp, Haiyan Xu, Marina Shikhman, Efrat Schori, Jack M. Gorman, T. Conrad Gilliam

Journal:

Biological Psychiatry

Year:

2005

Language:

english

File:

PDF, 172 KB

english, 2005

48

Disease Gene Prioritization Using Network and Feature

Xie, Bingqing, Agam, Gady, Balasubramanian, Sandhya, Xu, Jinbo, Gilliam, T. Conrad, Maltsev, Natalia, Börnigen, Daniela

Journal:

Journal of Computational Biology

Year:

2015

Language:

english

File:

PDF, 232 KB

english, 2015

49

Screen for expanded FMR1 alleles in patients with essential tremor

Dolores Garcia Arocena, Elan D. Louis, Flora Tassone, T. Conrad Gilliam, Ruth Ottman, Sébastien Jacquemont, Paul J. Hagerman

Journal:

Movement Disorders

Year:

2004

Language:

english

File:

PDF, 68 KB

english, 2004

50

10.1038/3030

Wang, Ching H., Gavrilov, Dimitar K., Shi, Xiangyang, Das, Kamna, Gilliam, T. Conrad

Journal:

Nature Genetics

Year:

1998

Language:

english

File:

PDF, 55 KB

english, 1998

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