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The publication data currently available has been vetted by Vanderbilt faculty, staff, administrators and trainees. The data itself is retrieved directly from NCBI's PubMed and is automatically updated on a weekly basis to ensure accuracy and completeness.

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Results: 1 to 10 of 20

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Integrative genomics identifies 7p11.2 as a novel locus for fever and clinical stress response in humans.
Ferguson JF, Meyer NJ, Qu L, Xue C, Liu Y, DerOhannessian SL, Rushefski M, Paschos GK, Tang S, Schadt EE, Li M, Christie JD, Reilly MP
(2015) Hum Mol Genet 24: 1801-12
MeSH Terms: Adolescent, Adult, Aged, Animals, Chromosomes, Human, Pair 7, European Continental Ancestry Group, Female, Fever, Genetic Loci, Genome-Wide Association Study, Humans, Lipopolysaccharides, Male, Mice, Middle Aged, Polymorphism, Single Nucleotide, Regulatory Elements, Transcriptional, Sepsis, Stress, Physiological, Wounds and Injuries, Young Adult
Added January 20, 2015
0 Communities
1 Members
0 Resources
21 MeSH Terms
CUX1 is a haploinsufficient tumor suppressor gene on chromosome 7 frequently inactivated in acute myeloid leukemia.
McNerney ME, Brown CD, Wang X, Bartom ET, Karmakar S, Bandlamudi C, Yu S, Ko J, Sandall BP, Stricker T, Anastasi J, Grossman RL, Cunningham JM, Le Beau MM, White KP
(2013) Blood 121: 975-83
MeSH Terms: Acute Disease, Animals, Blotting, Western, Cell Line, Tumor, Chromosome Deletion, Chromosomes, Human, Pair 7, Drosophila melanogaster, Gene Expression Profiling, Haploinsufficiency, HeLa Cells, Homeodomain Proteins, Humans, Interleukin Receptor Common gamma Subunit, K562 Cells, Leukemia, Myeloid, Mice, Mice, Inbred NOD, Mice, Knockout, Mice, SCID, Nuclear Proteins, RNA Interference, Repressor Proteins, Reverse Transcriptase Polymerase Chain Reaction, Transcription Factors, Translocation, Genetic, Tumor Suppressor Proteins, U937 Cells, Xenograft Model Antitumor Assays
Added March 28, 2014
0 Communities
1 Members
0 Resources
28 MeSH Terms
Genomic imbalances in benign metastasizing leiomyoma: characterization by conventional karyotypic, fluorescence in situ hybridization, and whole genome SNP array analysis.
Bowen JM, Cates JM, Kash S, Itani D, Gonzalez A, Huang D, Oliveira A, Bridge JA
(2012) Cancer Genet 205: 249-54
MeSH Terms: Chromosome Deletion, Chromosomes, Human, Pair 7, Female, Gene Rearrangement, Humans, In Situ Hybridization, Fluorescence, Karyotyping, Leiomyoma, Lung Neoplasms, Middle Aged, Muscle Neoplasms, Oligonucleotide Array Sequence Analysis, Polymorphism, Single Nucleotide, Thigh, Uterine Neoplasms
Added March 15, 2013
0 Communities
1 Members
0 Resources
15 MeSH Terms
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D, Chu SH, Moreau MP, Gupta AR, Thomson SA, Mason CE, Bilguvar K, Celestino-Soper PB, Choi M, Crawford EL, Davis L, Wright NR, Dhodapkar RM, DiCola M, DiLullo NM, Fernandez TV, Fielding-Singh V, Fishman DO, Frahm S, Garagaloyan R, Goh GS, Kammela S, Klei L, Lowe JK, Lund SC, McGrew AD, Meyer KA, Moffat WJ, Murdoch JD, O'Roak BJ, Ober GT, Pottenger RS, Raubeson MJ, Song Y, Wang Q, Yaspan BL, Yu TW, Yurkiewicz IR, Beaudet AL, Cantor RM, Curland M, Grice DE, Günel M, Lifton RP, Mane SM, Martin DM, Shaw CA, Sheldon M, Tischfield JA, Walsh CA, Morrow EM, Ledbetter DH, Fombonne E, Lord C, Martin CL, Brooks AI, Sutcliffe JS, Cook EH, Geschwind D, Roeder K, Devlin B, State MW
(2011) Neuron 70: 863-85
MeSH Terms: Adolescent, Cadherins, Calcium-Binding Proteins, Cell Adhesion Molecules, Neuronal, Child, Child Development Disorders, Pervasive, Child, Preschool, Chromosomes, Human, Pair 16, Chromosomes, Human, Pair 7, Chromosomes, Human, X, DNA Copy Number Variations, Family Health, Female, Gene Duplication, Gene Expression Profiling, Genome-Wide Association Study, Genotype, Humans, Male, Nerve Tissue Proteins, Neural Cell Adhesion Molecules, Oligonucleotide Array Sequence Analysis, Phenotype, Proteins, Siblings, Ubiquitin Thiolesterase, Ubiquitin-Specific Peptidase 7, Williams Syndrome
Added February 20, 2014
0 Communities
1 Members
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28 MeSH Terms
Atopy history and the genomics of wheezing after influenza vaccination in children 6-59 months of age.
Miller EK, Dumitrescu L, Cupp C, Dorris S, Taylor S, Sparks R, Fawkes D, Frontiero V, Rezendes AM, Marchant C, Edwards KM, Crawford DC
(2011) Vaccine 29: 3431-7
MeSH Terms: Asthma, Child, Preschool, Chromosomes, Human, Pair 7, Clinical Trials as Topic, Female, Genome-Wide Association Study, Genotype, Humans, Infant, Influenza Vaccines, Influenza, Human, Male, Pilot Projects, Polymorphism, Single Nucleotide, Respiratory Sounds, Risk Factors
Added December 10, 2013
0 Communities
1 Members
0 Resources
16 MeSH Terms
A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3.
Kaplan RC, Petersen AK, Chen MH, Teumer A, Glazer NL, Döring A, Lam CS, Friedrich N, Newman A, Müller M, Yang Q, Homuth G, Cappola A, Klopp N, Smith H, Ernst F, Psaty BM, Wichmann HE, Sawyer DB, Biffar R, Rotter JI, Gieger C, Sullivan LS, Völzke H, Rice K, Spyroglou A, Kroemer HK, Ida Chen YD, Manolopoulou J, Nauck M, Strickler HD, Goodarzi MO, Reincke M, Pollak MN, Bidlingmaier M, Vasan RS, Wallaschofski H
(2011) Hum Mol Genet 20: 1241-51
MeSH Terms: Aged, Chromosomes, Human, Pair 7, Cohort Studies, European Continental Ancestry Group, Female, Genome-Wide Association Study, Humans, Insulin-Like Growth Factor Binding Protein 3, Insulin-Like Growth Factor I, Male, Polymorphism, Single Nucleotide
Added May 21, 2014
1 Communities
1 Members
0 Resources
11 MeSH Terms
Genome-wide analysis of copy number variation in type 1 diabetes.
Grayson BL, Smith ME, Thomas JW, Wang L, Dexheimer P, Jeffrey J, Fain PR, Nanduri P, Eisenbarth GS, Aune TM
(2010) PLoS One 5: e15393
MeSH Terms: Adult, Chromosome Deletion, Chromosomes, Human, Pair 13, Chromosomes, Human, Pair 2, Chromosomes, Human, Pair 6, Chromosomes, Human, Pair 7, Chromosomes, Human, Pair 8, Cohort Studies, DNA Copy Number Variations, Diabetes Mellitus, Type 1, Gene Deletion, Gene Frequency, Genetic Predisposition to Disease, Genetic Variation, Genome-Wide Association Study, Humans, Oligonucleotide Array Sequence Analysis, Polymorphism, Single Nucleotide, Risk Factors, Twins, Monozygotic
Added December 10, 2013
1 Communities
1 Members
0 Resources
20 MeSH Terms
MET amplification occurs with or without T790M mutations in EGFR mutant lung tumors with acquired resistance to gefitinib or erlotinib.
Bean J, Brennan C, Shih JY, Riely G, Viale A, Wang L, Chitale D, Motoi N, Szoke J, Broderick S, Balak M, Chang WC, Yu CJ, Gazdar A, Pass H, Rusch V, Gerald W, Huang SF, Yang PC, Miller V, Ladanyi M, Yang CH, Pao W
(2007) Proc Natl Acad Sci U S A 104: 20932-7
MeSH Terms: Adenocarcinoma, Antineoplastic Agents, Chromosomes, Human, Pair 7, Cohort Studies, DNA Mutational Analysis, Drug Resistance, Neoplasm, ErbB Receptors, Erlotinib Hydrochloride, Gefitinib, Gene Expression Regulation, Neoplastic, Humans, In Situ Hybridization, Fluorescence, Lung Neoplasms, Mutation, Protein Kinase Inhibitors, Proto-Oncogene Proteins c-met, Quinazolines
Added March 24, 2014
0 Communities
1 Members
0 Resources
17 MeSH Terms
A genetic variant that disrupts MET transcription is associated with autism.
Campbell DB, Sutcliffe JS, Ebert PJ, Militerni R, Bravaccio C, Trillo S, Elia M, Schneider C, Melmed R, Sacco R, Persico AM, Levitt P
(2006) Proc Natl Acad Sci U S A 103: 16834-9
MeSH Terms: Alleles, Autistic Disorder, Base Sequence, Case-Control Studies, Chromosome Mapping, Chromosomes, Human, Pair 7, DNA, Female, Genetic Predisposition to Disease, Genetic Variation, Genotype, Humans, Linkage Disequilibrium, Male, Polymorphism, Single Nucleotide, Promoter Regions, Genetic, Proto-Oncogene Proteins, Proto-Oncogene Proteins c-met, Receptors, Growth Factor, Transcription Factors, Transcription, Genetic
Added February 20, 2014
0 Communities
1 Members
0 Resources
21 MeSH Terms
Analysis of the RELN gene as a genetic risk factor for autism.
Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, DeLong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA
(2005) Mol Psychiatry 10: 563-71
MeSH Terms: 5' Untranslated Regions, Autistic Disorder, Cell Adhesion Molecules, Neuronal, Chromosomes, Human, Pair 7, European Continental Ancestry Group, Extracellular Matrix Proteins, Female, Genetic Predisposition to Disease, Genotype, Humans, Infant, Linkage Disequilibrium, Male, Nerve Tissue Proteins, Pedigree, Polymorphism, Single Nucleotide, Serine Endopeptidases
Added February 20, 2014
0 Communities
1 Members
0 Resources
17 MeSH Terms