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Items where Division is "School of Public Health > Human Genetics" and Year is 2015

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Number of items: 26.


Ashraf, Alexandria (2015) Analysis of support group availability for adult-onset neurological disorders in central Appalachian region of the United States. Master Essay, University of Pittsburgh.


Baron, RV and Conley, YP and Gorin, MB and Weeks, DE (2015) dbVOR: A database system for importing pedigree, phenotype and genotype data and exporting selected subsets. BMC Bioinformatics, 16 (1).

Beadling, Randall (2015) Implementing array comparative genomic hybridization in male infertility diagnostics. Master Essay, University of Pittsburgh.

Beadling, Randall (2015) Restoring spermatogenesis: Lentiviral gene therapy for male infertility in mice. Master's Thesis, University of Pittsburgh. (Unpublished)

Breski, Megan (2015) Allele specific approach to study histone demethylation using engineered KDM4A- (2)-Ketoglutarate pairs. Master's Thesis, University of Pittsburgh. (Unpublished)

Bui, DK and Jiang, Y and Wei, X and Ortube, MC and Weeks, DE and Conley, YP and Gorin, MB (2015) Genetic ME-a visualization application for merging and editing pedigrees for genetic studies Medical Informatics and Decision Making. BMC Research Notes, 8 (1).


Chen, W and Brehm, JM and Lin, J and Wang, T and Forno, E and Acosta-Pérez, E and Boutaoui, N and Canino, G and Celedón, JC (2015) Expression Quantitative Trait Loci (eQTL) mapping in Puerto Rican children. PLoS ONE, 10 (3).

Clinard, Kristin (2015) Research participation in the Duchenne muscular dystrophy community: parent perceived barriers and their impact on families. Master's Thesis, University of Pittsburgh. (Unpublished)


Ferraro, Jessica (2015) Oral health, genetics, and public health. Master Essay, University of Pittsburgh.


Geskin, A and Legowski, E and Chakka, A and Chandran, UR and Barmada, MM and LaFramboise, WA and Berg, J and Jacobson, RS (2015) Needs assessment for research use of high- throughput sequencing at a large academic medical center. PLoS ONE, 10 (6).


Hafren, L and Einarsdottir, E and Kentala, E and Hammaren-Malmi, S and Bhutta, MF and MacArthur, CJ and Wilmot, B and Casselbrant, M and Conley, YP and Weeks, DE and Mandel, EM and Vaarala, O and Kallio, A and Melin, M and Nieminen, JK and Leinonen, E and Kere, J and Mattila, PS (2015) Predisposition to childhood otitis media and genetic polymorphisms within the toll-like receptor 4 (TLR4) Locus. PLoS ONE, 10 (7).


Irani, Afifa (2015) Investigation of the common MELAS mutation in the Northwestern Pennsylvania Amish community: mutation frequency and effectiveness of an educational intervention. Master's Thesis, University of Pittsburgh. (Unpublished)


Kim, SH and Herazo-Maya, JD and Kang, DD and Juan-Guardela, BM and Tedrow, J and Martinez, FJ and Sciurba, FC and Tseng, GC and Kaminski, N (2015) Integrative phenotyping framework (iPF): Integrative clustering of multiple omics data identifies novel lung disease subphenotypes. BMC Genomics, 16 (1).


Labilloy, Anatália (2015) Signaling pathways in cell models of Fabry disease nephropathy. Doctoral Dissertation, University of Pittsburgh. (Unpublished)

Lawrence, Chad (2015) ATM copy number loss as a biomarker for radioresistance in urothelial bladder cancer cell lines. Master's Thesis, University of Pittsburgh. (Unpublished)

Liao, S and Hartmaier, RJ and McGuire, KP and Puhalla, SL and Luthra, S and Chandran, UR and Ma, T and Bhargava, R and Modugno, F and Davidson, NE and Benz, S and Lee, AV and Tseng, GC and Oesterreich, S (2015) The molecular landscape of premenopausal breast cancer. Breast Cancer Research, 17 (1). ISSN 1465-5411


Mancini, C and Orsi, L and Guo, Y and Li, J and Chen, Y and Wang, F and Tian, L and Liu, X and Zhang, J and Jiang, H and Nmezi, BS and Tatsuta, T and Giorgio, E and Di Gregorio, E and Cavalieri, S and Pozzi, E and Mortara, P and Caglio, MM and Balducci, A and Pinessi, L and Langer, T and Padiath, QS and Hakonarson, H and Zhang, X and Brusco, A (2015) An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2. BMC Medical Genetics, 16 (1).


Niemsiri, V and Wang, X and Pirim, D and Radwan, ZH and Bunker, CH and Barmada, MM and Kamboh, MI and Demirci, FY (2015) Genetic contribution of SCARB1 variants to lipid traits in African Blacks: A candidate gene association study. BMC Medical Genetics, 16 (1).

Niemsiri, Vipavee (2015) Genetic influence of sequence variants in SCARB1 and ABCA1 genes on major lipid traits: a candidate gene association study. Doctoral Dissertation, University of Pittsburgh. (Unpublished)

Nunziato-Virga, Stephanie (2015) Contribution of the candidate genes for primary lymphedema to secondary lymphedema and chronic pain in post-mastectomy patients. Master's Thesis, University of Pittsburgh. (Unpublished)


Orlova, Ekaterina (2015) G,WAS going on? Putative regulatory function of GWAS-identified markers of susceptibility to acute appendicitis. Master's Thesis, University of Pittsburgh. (Unpublished)


Ren, Y and Suzuki, H and Jagarlamudi, K and Golnoski, K and McGuire, M and Lopes, R and Pachnis, V and Rajkovic, A (2015) Lhx8 regulates primordial follicle activation and postnatal folliculogenesis. BMC Biology, 13 (1).


Talzhanov, Yerkebulan (2015) A new workflow of fetal DNA prediction from cell-free DNA in maternal plasma. Doctoral Dissertation, University of Pittsburgh. (Unpublished)


Velazquez, Enrique Israel (2015) Alternatives to relational databases in precision medicine: comparison of NOSQL approaches for big data storage using supercomputers. Doctoral Dissertation, University of Pittsburgh. (Unpublished)


Weinreb, NJ and Finegold, DN and Feingold, E and Zeng, Z and Rosenbloom, BE and Shankar, SP and Amato, D (2015) Evaluation of disease burden and response to treatment in adults with type 1 gaucher disease using a validated disease severity scoring system (DS3). Orphanet Journal of Rare Diseases, 10 (1).

Wolf, ZT and Brand, HA and Shaffer, JR and Leslie, EJ and Arzi, B and Willet, CE and Cox, TC and McHenry, T and Narayan, N and Feingold, E and Wang, X and Sliskovic, S and Karmi, N and Safra, N and Sanchez, C and Deleyiannis, FWB and Murray, JC and Wade, CM and Marazita, ML and Bannasch, DL (2015) Genome-Wide Association Studies in Dogs and Humans Identify ADAMTS20 as a Risk Variant for Cleft Lip and Palate. PLoS Genetics, 11 (3). ISSN 1553-7390

This list was generated on Mon May 27 10:59:23 2024 EDT.