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Knowledge and Acceptability of Pap Smears, Self-sampling and HPV Vaccination among Adult Women in Kenya. 

Rositch, A. F.; Gatuguta, A.; Choi, R. Y.; Guthrie, B. L.; Mackelprang, R. D.; Bosire, R; Manyara, L.; Kiarie, J. N.; Smith, J. S.; Farquhar, C. (2012)
OBJECTIVES: Our study aimed to assess adult women's knowledge of human papillomavirus (HPV) and cervical cancer, and characterize their attitudes towards potential screening and prevention strategies. METHODS: Women ...
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Whole-genome sequencing in an autism multiplex family 

Otieno, F. G.; Shi, L.; Zhang, X.; Golhar, R.; He, M.; Hou, C.; Kim, C.; Keating, B.; Lyon, G.J.; Wang, K.; Hakonarson, H. (BioMed Central, 2013)
Background: Autism spectrum disorders (ASDs) represent a group of childhood neurodevelopmental disorders that affect 1 in 88 children in the US. Previous exome sequencing studies on family trios have implicated a role for ...
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Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population 

Otieno, F. G.; Matsunami, Nori; Hensel, Charles H; Baird, Lisa; Stevens, Jeff; Otterud, Brith; Leppert, Tami; Varvil, Tena; Hadley, Dexter; Glessner, Joseph T; Pellegrino, Renata; Kim, Cecilia; Thomas, Kelly; Wang, Fengxiang; Ho, Karen; Christensen, Gerald B; Li, Dongying; Prekeris, Rytis; Lambert, Christophe G; Hakonarson, H.; Leppert, Mark F (BioMed Central, 2014)
Background: Genetics clearly plays a major role in the etiology of autism spectrum disorders (ASDs), but studies to date are only beginning to characterize the causal genetic variants responsible. Until recently, studies ...
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Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. 

Otieno, F. G.; Lanktree, M.B.; Guo, Y.; Murtaza, M.; Glessner, J.T. (Elsevier, 2011)
Height is a classic complex trait with common variants in a growing list of genes known to contribute to the phenotype. Using a genecentric genotyping array targeted toward cardiovascular-related loci, comprising 49,320 ...
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Health System Factors Affecting Uptake of Antenatal Care by Women of Reproductive Age in Kisumu County, Kenya 

Kilowua, Lydia; Otieno, Kennedy (International Journal of Public Health and Epidemiology Research, 2019)
This study sought to determine how health system factors affect antenatal care services uptake. A descriptive cross-sectional study design was adopted. The population under study was selected household members of the ...
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Nurses’ Perception on Healthcare Services Quality in Mission Hospitals in Kiambu County, Kenya 

Miriti, Kenneth; Yitambe, Andre; Nyamari, Jackim; Koome, Gilbert (AJOL, 2019-02)
BACKGROUND Despite adoption of quality improvement initiatives in Kenyan Health facilities, quality gains are not yet optimal in both public and private sector. The private sector, which includes mission hospitals, face ...
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Evaluation of Technical Efficiency of County Referral Hospitals in Kenya and Its Determinants 

Rithaa, Gilbert; Kosimbe, George; Yitambe, Andrew; Kithuka, Peter (International Journal of Advanced Medical and Health Research, 2019)
Government’s health expenditure as a percent of the total government budget is approximately 7% which falls below the target of 15% recommended by the World Health Organization. It is, therefore, important that the ...
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AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate. 

Otieno, F. G.; Falk, M.J.; Li, D.; Gai, X.; McCormick, E.; Place, E.; Lasorsa, F.M.; Hou, C.; Kim, C.E.; Abdel-Magid, N.; Vazquez, L.; Mentch, F.D.; Chiavacci, R. M.; Liang, J.; Liu, X.; Jiang, H.; Giannuzzi, G.; Marsh, E.D.; Yiran, G.; Tian, L.; Palmieri, F.; Hakonarson, H. (2014)
BACKGROUND: Whole exome sequencing (WES) offers a powerful diagnostic tool to rapidly and efficiently sequence all coding genes in individuals presenting for consideration of phenotypically and genetically heterogeneous ...
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Erratum to: AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate 

Otieno, F. G.; Falk, M.J.; Li, D.; Gai, X.; McCormick, E.; Place, E.; Lasorsa, F.M.; Hou, C.; Kim, C.E.; Abdel-Magid, N.; Vazquez, L.; Mentch, F.D.; Chiavacci, R. M.; Liang, J.; Liu, X.; Jiang, H.; Giannuzzi, G.; Marsh, E.D.; Yiran, G.; Tian, L.; Palmieri, F.; Hakonarson, H. (2014)
BACKGROUND: Whole exome sequencing (WES) offers a powerful diagnostic tool to rapidly and efficiently sequence all coding genes in individuals presenting for consideration of phenotypically and genetically heterogeneous ...
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Whole-genome DNA/RNA sequencing identifies truncating mutations in RBCK1 in a novel Mendelian disease with neuromuscular and cardiac involvement 

Otieno, F. G.; Wang, Kai; Kim, Cecilia; Bradfield, Jonathan; Guo, Yunfei; Toskala, Elina; Hou, Cuiping; Thomas, Kelly; Cardinale, Christopher; Lyon, Gholson J; Golhar, Ryan; Hakonarson, Hakon (BioMed Central, 2013)
Background: Whole-exome sequencing has identified the causes of several Mendelian diseases by analyzing multiple unrelated cases, but it is more challenging to resolve the cause of extremely rare and suspected Mendelian ...
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AuthorOtieno, F. G. (6)Hakonarson, H. (4)Hou, C. (3)Abdel-Magid, N. (2)Chiavacci, R. M. (2)Falk, M.J. (2)Gai, X. (2)Giannuzzi, G. (2)Jiang, H. (2)Kim, C.E. (2)... View MoreSubjectAntenatal care uptake (1)Asphyxia (1)Awareness, Knowledge, Cervical Cancer (1)Biomass fuels (1)Case/control study (1)County referral hospitals (1)Data envelopment analysis (1)Distance (1)DNA sequence variants (1)Familial autism (1)... View MoreDate Issued2019 (7)2014 (4)2013 (3)2012 (1)2011 (1)

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