Search Results - "Lashley, Kerrie"

A genome-wide association study of hypertension and blood pressure in African Americans by Adeyemo, Adebowale, Gerry, Norman, Chen, Guanjie, Herbert, Alan, Doumatey, Ayo, Huang, Hanxia, Zhou, Jie, Lashley, Kerrie, Chen, Yuanxiu, Christman, Michael, Rotimi, Charles

“…The evidence for the existence of genetic susceptibility variants for the common form of hypertension ("essential hypertension") remains weak and inconsistent…”
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A Possible Accessory Muscle of the Serratus Posterior Superior Muscle by Lashley, Kerrie, Granite, Guinevere

“…Anatomical variation is defined as the normal range of possibilities in the topography and morphology of body structures. In contrast, an anomaly is any…”
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Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays by Dagnall, Casey L, Morton, Lindsay M, Hicks, Belynda D, Li, Shengchao, Zhou, Weiyin, Karlins, Eric, Teshome, Kedest, Chowdhury, Salma, Lashley, Kerrie S, Sampson, Joshua N, Robison, Leslie L, Armstrong, Gregory T, Bhatia, Smita, Radloff, Gretchen A, Davies, Stella M, Tucker, Margaret A, Yeager, Meredith, Chanock, Stephen J

“…The recommended genomic DNA input requirements for whole genome single nucleotide polymorphism microarrays can limit the scope of molecular epidemiological…”
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Relationships Among Obesity, Inflammation, and Insulin Resistance in African Americans and West Africans by Doumatey, Ayo P, Lashley, Kerrie S, Huang, Hanxia, Zhou, Jie, Chen, Guanjie, Amoah, Albert, Agyenim-Boateng, Kofi, Oli, Johnnie, Fasanmade, Olufemi, Adebamowo, Clement A, Adeyemo, Adebowale A, Rotimi, Charles N

“…Several research studies in different populations indicate that inflammation may be the link between obesity and insulin resistance (IR). However, this…”
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A Genome-Wide Search for Linkage to Renal Function Phenotypes in West Africans With Type 2 Diabetes by Chen, Guanjie, MD, Adeyemo, Adebowale A., MD, Zhou, Jie, BS, Chen, Yuanxiu, MD, PhD, Doumatey, Ayo, MS, Lashley, Kerrie, BS, Huang, Hanxia, MD, Amoah, Albert, MD, PhD, Agyenim-Boateng, Kofi, MD, Eghan, Benjamin A., MD, Okafor, Godfrey, MD, Acheampong, Joseph, MD, Oli, Johnnie, MD, Fasanmade, Olufemi, MD, Johnson, Thomas, MD, Rotimi, Charles, PhD

“…Background Reduced renal function often is a major consequence of diabetes and hypertension. Although several indices of renal function (eg, creatinine…”
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Rare Case of an Accessory Left Vertebral Artery on the Aortic Arch by Granite, Guinevere, Lashley, Kerrie

“…Vascular variations of the head and neck are common, but often go unnoticed because they generally do not present clear clinical symptoms. Unawareness of the…”
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Case Study: A Possible Accessory Muscle of the Serratus Posterior Superior Muscle by Lashley, Kerrie Samantha, Granite‐Cohn, Guinevere

“…Anatomical variation is defined as the normal range of possibilities in the topography and morphology of body structures. In contrast, congenital anomaly is…”
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A variant in CDKAL1 influences insulin response and risk of type 2 diabetes by Steinthorsdottir, Valgerdur, Stefansson, Kari, Thorleifsson, Gudmar, Reynisdottir, Inga, Benediktsson, Rafn, Jonsdottir, Thorbjorg, Walters, G Bragi, Styrkarsdottir, Unnur, Gretarsdottir, Solveig, Emilsson, Valur, Ghosh, Shyamali, Baker, Adam, Snorradottir, Steinunn, Bjarnason, Hjordis, Ng, Maggie C Y, Hansen, Torben, Bagger, Yu, Wilensky, Robert L, Reilly, Muredach P, Adeyemo, Adebowale, Chen, Yuanxiu, Zhou, Jie, Gudnason, Vilmundur, Chen, Guanjie, Huang, Hanxia, Lashley, Kerrie, Doumatey, Ayo, So, Wing-Yee, Ma, Ronald C Y, Andersen, Gitte, Borch-Johnsen, Knut, Jorgensen, Torben, van Vliet-Ostaptchouk, Jana V, Hofker, Marten H, Wijmenga, Cisca, Christiansen, Claus, Rader, Daniel J, Rotimi, Charles, Gurney, Mark, Chan, Juliana C N, Pedersen, Oluf, Sigurdsson, Gunnar, Gulcher, Jeffrey R, Thorsteinsdottir, Unnur, Kong, Augustine

“…We conducted a genome-wide association study for type 2 diabetes (T2D) in Icelandic cases and controls, and we found that a previously described variant in the…”
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Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1 by Kocak, Hande, Ballew, Bari J, Bisht, Kamlesh, Eggebeen, Rebecca, Hicks, Belynda D, Suman, Shalabh, O'Neil, Adri, Giri, Neelam, Maillard, Ivan, Alter, Blanche P, Keegan, Catherine E, Nandakumar, Jayakrishnan, Savage, Sharon A

“…Germline mutations in telomere biology genes cause dyskeratosis congenita (DC), an inherited bone marrow failure and cancer predisposition syndrome. DC is a…”
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Sciatic Nerve Bilateral High Bifurcation between the Two Heads of the Piriformis Muscle in a 92-year-old White Female Donor: A Case Report by Wands, Kayla C, Samuel, Amanda, Sparks, Andrea, Meshida, Keiko, Wind, Gary, Lashley, Kerrie, Wolf, Kieran, Dau, Georgia, Kalima, Jean B, Koo, Caitlyn, Rasmussen, Austin, Tang, Betsy, Granite, Guinevere

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Novel FANCI mutations in Fanconi anemia with VACTERL association by Savage, Sharon A., Ballew, Bari J., Giri, Neelam, Chandrasekharappa, Settara C., Ameziane, Najim, de Winter, Johan, Alter, Blanche P.

“…Fanconi anemia (FA) is an inherited bone marrow failure syndrome caused by mutations in DNA repair genes; some of these patients may have features of the…”
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Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-Up by Burris, Ashley M., DO, Ballew, Bari J., PhD, Kentosh, Joshua B., DO, Turner, Clesson E., MD, Norton, Scott A., MD, MPH, Giri, Neelam, MD, Alter, Blanche P., MD, MPH, Nellan, Anandani, MD, Gamper, Christopher, MD, PhD, Hartman, Kip R., MD, Savage, Sharon A., MD

“…Abstract Background Hoyeraal-Hreidarsson syndrome is a dyskeratosis congenita–related telomere biology disorder that presents in infancy with intrauterine…”
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Polymorphism of the endothelial nitric oxide synthase gene is associated with diabetic retinopathy in a cohort of West Africans by Chen, Yuanxiu, Huang, Hanxia, Zhou, Jie, Doumatey, Ayo, Lashley, Kerrie, Chen, Guanjie, Agyenim-Boateng, Kofi, Eghan, Benjamin A, Acheampong, Joseph, Fasanmade, Olufemi, Johnson, Thomas, Akinsola, Folasade B, Okafor, Godfrey, Oli, Johnnie, Ezepue, Felix, Amoah, Albert, Akafo, Stephen, Adeyemo, Adebowale, Rotimi, Charles N

“…In addition to chronic hyperglycemia, there is increasing evidence that genetic factors may be important in the development of diabetes retinopathy (DR)…”
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A Genome-Wide Association Study of Hypertension and Blood Pressure in African Americans: e1000564 by Adeyemo, Adebowale, Gerry, Norman, Chen, Guanjie, Herbert, Alan, Doumatey, Ayo, Huang, Hanxia, Zhou, Jie, Lashley, Kerrie, Chen, Yuanxiu, Christman, Michael, Rotimi, Charles

“…The evidence for the existence of genetic susceptibility variants for the common form of hypertension ("essential hypertension") remains weak and inconsistent…”
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Genome-wide search for susceptibility genes to type 2 diabetes in West Africans: Potential role of C-peptide by Chen, Guanjie, Adeyemo, Adebowale, Zhou, Jie, Chen, Yuanxiu, Huang, Hanxia, Doumatey, Ayo, Lashley, Kerrie, Agyenim-Boateng, Kofi, Eghan, Benjamin A, Acheampong, Joseph, Fasanmade, Olufemi, Johnson, Thomas, Okafor, Godfrey, Oli, Johnnie, Amoah, Albert, Rotimi, Charles

“…Abstract C-peptide is a substance that the pancreas releases into the circulation in equimolar amounts to insulin and has demonstrated important physiological…”
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A variant in CDKAL1 influences insulin response and risk of type 2 diabetes by STEINTHORSDOTTIR, Valgerdur, THORLEIFSSON, Gudmar, BAKER, Adam, SNORRADOTTIR, Steinunn, BJARNASON, Hjordis, NG, Maggie C. Y, HANSEN, Torben, BAGGER, Yu, WILENSKY, Robert L, REILLY, Muredach P, ADEYEMO, Adebowale, YUANXIU CHEN, REYNISDOTTIR, Inga, JIE ZHOU, GUDNASON, Vilmundur, GUANJIE CHEN, HANXIA HUANG, LASHLEY, Kerrie, DOUMATEY, Ayo, SO, Wing-Yee, MA, Ronald C. Y, ANDERSEN, Gitte, BORCH-JOHNSEN, Knut, BENEDIKTSSON, Rafn, JORGENSEN, Torben, VAN VLIET-OSTAPTCHOUK, Jana V, HOFKER, Marten H, WIJMENGA, Cisca, CHRISTIANSEN, Claus, RADER, Daniel J, ROTIMI, Charles, GURNEY, Mark, CHAN, Juliana C. N, PEDERSEN, Oluf, JONSDOTTIR, Thorbjorg, SIGURDSSON, Gunnar, GULCHER, Jeffrey R, THORSTEINSDOTTIR, Unnur, KONG, Augustine, STEFANSSON, Kari, WALTERS, G. Bragi, STYRKARSDOTTIR, Unnur, GRETARSDOTTIR, Solveig, EMILSSON, Valur, GHOSH, Shyamali

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Comparative study of matrix metalloproteinase expression between African American and Caucasian Women by Mason, Jacquline A, Yancy, Haile F, Lashley, Kerrie, Jett, Marty, Day, Agnes A

“…To date there are 26 human matrix metalloproteinases (MMPs) which are classified according to their substrate specificity and structural similarities. The four…”
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