Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Clare Knebusch"'
Autor:
Martha Sajatovic, Lynn Herrmann, Clare Knebusch, Kaylee Sarna, Alan Lerner, Edna Fuentes-Casiano, Christopher Burant
Publikováno v:
Innovation in Aging. 6:487-488
Racial and ethnic minorities are under-represented in dementia research. We tested a conceptually-driven health communication approach targeting evidence-based barriers and facilitators to research participation vs. dementia awareness training. Input
Autor:
William K. Scott, Clare Knebusch, Laura D. Nations, Anna C. Cummings, Denise Fuzzell, Renee Laux, Lynne L. McFarland, Ioanna Konidari, Lan Jiang, Laura Caywood, Margaret A. Pericak-Vance, Jacob L. McCauley, Lori Reinhart-Mercer, Digna R. Velez Edwards, Michael L. Cuccaro, John R. Gilbert, Michael G. Tramontana, Jonathan L. Haines
Publikováno v:
Annals of Human Genetics. 76:342-351
To identify novel late-onset Alzheimer disease (LOAD) risk genes, we have analysed Amish populations of Ohio and Indiana. We performed genome-wide SNP linkage and association studies on 798 individuals (109 with LOAD). We tested association using the
Autor:
John Gilbert, Clare Knebusch, William K. Scott, Marilyn Creason, Charles E. Jackson, Lan Jiang, Margaret A. Pericak-Vance, Paul Gallins, Jonathan L. Haines, Digna R. Velez Edwards, Denise Fuzzell, Laura Caywood
Publikováno v:
Annals of Human Genetics. 75:516-528
Successful aging (SA) is a multidimensional phenotype involving preservation of cognitive ability, physical function, and social engagement throughout life. Multiple components of SA are heritable, supporting a genetic component. The Amish are geneti
Autor:
Jonathan L. Haines, Lynne L. McFarland, Lan Jiang, William K. Scott, Amy E. Crunk, Anna C. Cummings, Denise Fuzzell, Stephen L. Lee, Clare Knebusch, Charles E. Jackson, Jacob L. McCauley, Paul Gallins, Margaret A. Pericak-Vance
Publikováno v:
Annals of Human Genetics. 75:351-358
Summary Parkinson disease (PD) is a common complex neurodegenerative disorder with an underlying genetic etiology that has been difficult to dissect. Although some PD risk genes have been discovered, most of the underlying genetic etiology remains un
Autor:
Anna C, Cummings, Lan, Jiang, Digna R, Velez Edwards, Jacob L, McCauley, Renee, Laux, Lynne L, McFarland, Denise, Fuzzell, Clare, Knebusch, Laura, Caywood, Lori, Reinhart-Mercer, Laura, Nations, John R, Gilbert, Ioanna, Konidari, Michael, Tramontana, Michael L, Cuccaro, William K, Scott, Margaret A, Pericak-Vance, Jonathan L, Haines
Publikováno v:
Annals of human genetics. 76(5)
To identify novel late-onset Alzheimer disease (LOAD) risk genes, we have analysed Amish populations of Ohio and Indiana. We performed genome-wide SNP linkage and association studies on 798 individuals (109 with LOAD). We tested association using the
Autor:
Lynne L. McFarland, William K. Scott, Clare Knebusch, Anna C. Cummings, Lan Jiang, Denise Fuzzell, Jonathan L. Haines, Laura Caywood, Margaret A. Pericak-Vance, Charles E. Jackson, Renee Laux, Lori Reinhart-Mercer, Jacob L. McCauley, Digna R. Velez Edwards
Publikováno v:
Alzheimer's & Dementia. 7
Autor:
Digna R Velez, Edwards, John R, Gilbert, Lan, Jiang, Paul J, Gallins, Laura, Caywood, Marilyn, Creason, Denise, Fuzzell, Clare, Knebusch, Charles E, Jackson, Margaret A, Pericak-Vance, Jonathan L, Haines, William K, Scott
Publikováno v:
Annals of human genetics. 75(4)
Successful aging (SA) is a multi-dimensional phenotype involving preservation of cognitive ability, physical function, and social engagement throughout life. Multiple components of SA are heritable, supporting a genetic component. The Old Order Amish
Autor:
Anna C, Cummings, Stephen L, Lee, Jacob L, McCauley, Lan, Jiang, Amy, Crunk, Lynne L, McFarland, Paul J, Gallins, Denise, Fuzzell, Clare, Knebusch, Charles E, Jackson, William K, Scott, Margaret A, Pericak-Vance, Jonathan L, Haines
Publikováno v:
Annals of human genetics. 75(3)
Parkinson disease (PD) is a common complex neurodegenerative disorder with an underlying genetic etiology that has been difficult to dissect. Although some PD risk genes have been discovered, most of the underlying genetic etiology remains unknown. T