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1.

Visuospatial and Verbal Memory Differences in Amish Individuals With Alzheimer Disease and Related Dementias.

Prough, Michael B; Zaman, Andrew; Caywood, Laura J; Clouse, Jason E; Herington, Sharlene D; Slifer, Susan H; Dorfsman, Daniel A; Adams, Larry A; Laux, Reneé A; Song, Yeunjoo E; Lynn, Audrey; Fuzzell, Denise; Fuzzell, Sarada L; Miller, Sherri D; Miskimen, Kristy; Main, Leighanne R; Osterman, Michael D; Ogrocki, Paula; Lerner, Alan J; Vance, Jeffery M; Haines, Jonathan L; Scott, William K; Pericak-Vance, Margaret; Cuccaro, Michael L.

Alzheimer Dis Assoc Disord; 37(3): 195-199, 2023.

Artículo en Inglés | MEDLINE | ID: mdl-37561946

2.

Identification of novel genes for age-at-onset of Alzheimer's disease by combining quantitative and survival trait analyses.

Li, Yi-Ju; Nuytemans, Karen; La, Jong Ok; Jiang, Rong; Slifer, Susan H; Sun, Shuming; Naj, Adam; Gao, Xiaoyi Raymond; Martin, Eden R.

Alzheimers Dement; 19(7): 3148-3157, 2023 07.

Artículo en Inglés | MEDLINE | ID: mdl-36738287

3.

Genetic variants in the SHISA6 gene are associated with delayed cognitive impairment in two family datasets.

Ramos, Jairo; Caywood, Laura J; Prough, Michael B; Clouse, Jason E; Herington, Sharlene D; Slifer, Susan H; Fuzzell, M Denise; Fuzzell, Sarada L; Hochstetler, Sherri D; Miskimen, Kristy L; Main, Leighanne R; Osterman, Michael D; Zaman, Andrew F; Whitehead, Patrice L; Adams, Larry D; Laux, Renee A; Song, Yeunjoo E; Foroud, Tatiana M; Mayeux, Richard P; St George-Hyslop, Peter; Ogrocki, Paula K; Lerner, Alan J; Vance, Jeffery M; Cuccaro, Michael L; Haines, Jonathan L; Pericak-Vance, Margaret A; Scott, William K.

Alzheimers Dement; 19(2): 611-620, 2023 02.

Artículo en Inglés | MEDLINE | ID: mdl-35490390

4.

Genome-wide enriched pathway analysis of acute post-radiotherapy pain in breast cancer patients: a prospective cohort study.

Lee, Eunkyung; Takita, Cristiane; Wright, Jean L; Slifer, Susan H; Martin, Eden R; Urbanic, James J; Langefeld, Carl D; Lesser, Glenn J; Shaw, Edward G; Hu, Jennifer J.

Hum Genomics; 13(1): 28, 2019 06 13.

Artículo en Inglés | MEDLINE | ID: mdl-31196165

5.

Properties of global- and local-ancestry adjustments in genetic association tests in admixed populations.

Martin, Eden R; Tunc, Ilker; Liu, Zhi; Slifer, Susan H; Beecham, Ashley H; Beecham, Gary W.

Genet Epidemiol; 42(2): 214-229, 2018 03.

Artículo en Inglés | MEDLINE | ID: mdl-29288582

6.

A common MUC5B promoter polymorphism and pulmonary fibrosis.

Seibold, Max A; Wise, Anastasia L; Speer, Marcy C; Steele, Mark P; Brown, Kevin K; Loyd, James E; Fingerlin, Tasha E; Zhang, Weiming; Gudmundsson, Gunnar; Groshong, Steve D; Evans, Christopher M; Garantziotis, Stavros; Adler, Kenneth B; Dickey, Burton F; du Bois, Roland M; Yang, Ivana V; Herron, Aretha; Kervitsky, Dolly; Talbert, Janet L; Markin, Cheryl; Park, Joungjoa; Crews, Anne L; Slifer, Susan H; Auerbach, Scott; Roy, Michelle G; Lin, Jia; Hennessy, Corinne E; Schwarz, Marvin I; Schwartz, David A.

N Engl J Med; 364(16): 1503-12, 2011 Apr 21.

Artículo en Inglés | MEDLINE | ID: mdl-21506741

7.

Genome Wide Association Study of Neuropathic Ocular Pain.

Huang, Jaxon J; Rodriguez, Daniel A; Slifer, Susan H; Martin, Eden R; Levitt, Roy C; Galor, Anat.

Ophthalmol Sci; 4(2): 100384, 2024.

Artículo en Inglés | MEDLINE | ID: mdl-37868788

8.

Founder population-specific weights yield improvements in performance of polygenic risk scores for Alzheimer disease in the Midwestern Amish.

Osterman, Michael D; Song, Yeunjoo E; Lynn, Audrey; Miskimen, Kristy; Adams, Larry D; Laux, Renee A; Caywood, Laura J; Prough, Michael B; Clouse, Jason E; Herington, Sharlene D; Slifer, Susan H; Fuzzell, Sarada L; Hochstetler, Sherri D; Main, Leighanne R; Dorfsman, Daniel A; Zaman, Andrew F; Ogrocki, Paula; Lerner, Alan J; Vance, Jeffery M; Cuccaro, Michael L; Scott, William K; Pericak-Vance, Margaret A; Haines, Jonathan L.

HGG Adv; 4(4): 100241, 2023 Oct 12.

Artículo en Inglés | MEDLINE | ID: mdl-37742071

9.

The genetic architecture of Alzheimer disease risk in the Ohio and Indiana Amish.

Osterman, Michael D; Song, Yeunjoo E; Adams, Larry D; Laux, Renee A; Caywood, Laura J; Prough, Michael B; Clouse, Jason E; Herington, Sharlene D; Slifer, Susan H; Lynn, Audrey; Fuzzell, M Denise; Fuzzell, Sarada L; Hochstetler, Sherri D; Miskimen, Kristy; Main, Leighanne R; Dorfsman, Daniel A; Ogrocki, Paula; Lerner, Alan J; Ramos, Jairo; Vance, Jeffery M; Cuccaro, Michael L; Scott, William K; Pericak-Vance, Margaret A; Haines, Jonathan L.

HGG Adv; 3(3): 100114, 2022 Jul 14.

Artículo en Inglés | MEDLINE | ID: mdl-35599847

10.

A modifier locus on chromosome 5 contributes to L1 cell adhesion molecule X-linked hydrocephalus in mice.

Tapanes-Castillo, Alexis; Weaver, Eli J; Smith, Robin P; Kamei, Yoshimasa; Caspary, Tamara; Hamilton-Nelson, Kara L; Slifer, Susan H; Martin, Eden R; Bixby, John L; Lemmon, Vance P.

Neurogenetics; 11(1): 53-71, 2010 Feb.

Artículo en Inglés | MEDLINE | ID: mdl-19565280

11.

Association Between Polymorphisms in DNA Damage Repair Genes and Radiation Therapy-Induced Early Adverse Skin Reactions in a Breast Cancer Population: A Polygenic Risk Score Approach.

Lee, Eunkyung; Eum, Sung Y; Slifer, Susan H; Martin, Eden R; Takita, Cristiane; Wright, Jean L; Hines, Robert B; Hu, Jennifer J.

Int J Radiat Oncol Biol Phys; 106(5): 948-957, 2020 04 01.

Artículo en Inglés | MEDLINE | ID: mdl-32007367

12.

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.

Ma, Deqiong; Salyakina, Daria; Jaworski, James M; Konidari, Ioanna; Whitehead, Patrice L; Andersen, Ashley N; Hoffman, Joshua D; Slifer, Susan H; Hedges, Dale J; Cukier, Holly N; Griswold, Anthony J; McCauley, Jacob L; Beecham, Gary W; Wright, Harry H; Abramson, Ruth K; Martin, Eden R; Hussman, John P; Gilbert, John R; Cuccaro, Michael L; Haines, Jonathan L; Pericak-Vance, Margaret A.

Ann Hum Genet; 73(Pt 3): 263-73, 2009 May.

Artículo en Inglés | MEDLINE | ID: mdl-19456320

13.

PLINK: Key Functions for Data Analysis.

Slifer, Susan H.

Curr Protoc Hum Genet; 97(1): e59, 2018 04.

Artículo en Inglés | MEDLINE | ID: mdl-30040203

14.

Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions.

Boyles, Abee L; Billups, Ashley V; Deak, Kristen L; Siegel, Deborah G; Mehltretter, Lorraine; Slifer, Susan H; Bassuk, Alexander G; Kessler, John A; Reed, Michael C; Nijhout, H Frederik; George, Timothy M; Enterline, David S; Gilbert, John R; Speer, Marcy C.

Environ Health Perspect; 114(10): 1547-52, 2006 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-17035141

15.

Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants.

Griswold, Anthony J; Dueker, Nicole D; Van Booven, Derek; Rantus, Joseph A; Jaworski, James M; Slifer, Susan H; Schmidt, Michael A; Hulme, William; Konidari, Ioanna; Whitehead, Patrice L; Cuccaro, Michael L; Martin, Eden R; Haines, Jonathan L; Gilbert, John R; Hussman, John P; Pericak-Vance, Margaret A.

Mol Autism; 6: 43, 2015.

Artículo en Inglés | MEDLINE | ID: mdl-26185613

16.

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.

Cukier, Holly N; Dueker, Nicole D; Slifer, Susan H; Lee, Joycelyn M; Whitehead, Patrice L; Lalanne, Eminisha; Leyva, Natalia; Konidari, Ioanna; Gentry, Ryan C; Hulme, William F; Booven, Derek Van; Mayo, Vera; Hofmann, Natalia K; Schmidt, Michael A; Martin, Eden R; Haines, Jonathan L; Cuccaro, Michael L; Gilbert, John R; Pericak-Vance, Margaret A.

Mol Autism; 5(1): 1, 2014 Jan 10.

Artículo en Inglés | MEDLINE | ID: mdl-24410847

17.

Association of AGTR1 with 18-month treatment outcome in late-life depression.

Kondo, Douglas G; Speer, Marcy C; Krishnan, K Ranga; McQuoid, Douglas R; Slifer, Susan H; Pieper, Carl F; Billups, Ashley V; Steffens, David C.

Am J Geriatr Psychiatry; 15(7): 564-72, 2007 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-17586781

18.

High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35.

Stamm, Demetra S; Rampersaud, Evadnie; Slifer, Susan H; Mehltretter, Lorraine; Siegel, Deborah G; Xie, Jianzhen; Hu-Lince, Diane; Craig, David W; Stephan, Dietrich A; George, Timothy M; Gilbert, John R; Speer, Marcy C.

Birth Defects Res A Clin Mol Teratol; 76(6): 499-505, 2006 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-16933213

19.

A genome-wide linkage analysis of dementia in the Amish.

Hahs, Daniel W; McCauley, Jacob L; Crunk, Amy E; McFarland, Lynne L; Gaskell, Perry C; Jiang, Lan; Slifer, Susan H; Vance, Jeffery M; Scott, William K; Welsh-Bohmer, Kathleen A; Johnson, Stephanie R; Jackson, Charles E; Pericak-Vance, Margaret A; Haines, Jonathan L.

Am J Med Genet B Neuropsychiatr Genet; 141B(2): 160-6, 2006 Mar 05.

Artículo en Inglés | MEDLINE | ID: mdl-16389594

20.

Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15.

Boyles, Abee L; Enterline, David S; Hammock, Preston H; Siegel, Deborah G; Slifer, Susan H; Mehltretter, Lorraine; Gilbert, John R; Hu-Lince, Diane; Stephan, Dietrich; Batzdorf, Ulrich; Benzel, Edward; Ellenbogen, Richard; Green, Barth A; Kula, Roger; Menezes, Arnold; Mueller, Diane; Oro', John J; Iskandar, Bermans J; George, Timothy M; Milhorat, Thomas H; Speer, Marcy C.

Am J Med Genet A; 140(24): 2776-85, 2006 Dec 15.

Artículo en Inglés | MEDLINE | ID: mdl-17103432

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