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301“…Ultimately, rare PTVs in the entire CEACAM gene family are associated with breast cancer risk in both European and African Americans with respective p-values of 1.75 × 10(–13) and 1.87 × 10(–04). …”
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302por Kim, Seung-Kyoon, Liu, Xihui, Park, Jongmin, Um, Dahun, Kilaru, Gokhul, Chiang, Cheng-Ming, Kang, Mingon, Huber, Kimberly M., Kang, Keunsoo, Kim, Tae-KyungEnlace del recurso
Publicado 2021
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303por Sze, Christie C., Ozark, Patrick A., Cao, Kaixiang, Ugarenko, Michal, Das, Siddhartha, Wang, Lu, Marshall, Stacy A., Rendleman, Emily J., Ryan, Caila A., Zha, Didi, Douillet, Delphine, Chen, Fei Xavier, Shilatifard, AliEnlace del recurso
Publicado 2020
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304por Freedman, Barry I., Langefeld, Carl D., Turner, JoLyn, Núñez, Marina, High, Kevin P., Spainhour, Mitzie, Hicks, Pamela J., Bowden, Donald W., Reeves-Daniel, Amber M., Murea, Mariana, Rocco, Michael V., Divers, Jasmin“…Familial aggregation of non-diabetic end stage renal disease (ESRD) is found in African Americans and variants in the apolipoprotein L1 gene (APOL1) contribute to this risk. …”
Publicado 2012
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305por Garza-Rodríguez, María Lourdes, Treviño, Víctor, Pérez-Maya, Antonio Alí, Rodríguez-Gutiérrez, Hazyadee Frecia, González-Escamilla, Moisés, Elizondo-Riojas, Miguel Ángel, Ramírez-Correa, Genaro A., Vidal-Gutiérrez, Oscar, Burciaga-Flores, Carlos Horacio, Pérez-Ibave, Diana Cristina“…Genetic counseling and cancer prevention strategies were provided for the family. According to the American College of Medical Genetics (ACMG) guidelines, this novel variant is considered a PVS1 variant (very strong evidence of pathogenicity), and it can be useful in association with clinical data for early surveillance and suitable treatment.…”
Publicado 2021
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306por Byambaa, Enkhmaa, Kim, Kyoungmi, Zhang, Wei, Truax, Kevin, Erdembileg, Anuurad, Berglund, Lars Folke“…Methods: Healthy Caucasian and African-American families were recruited from the general population (age range: 6–74 years, N=267). …”
Publicado 2020
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307por Howe, Anna S., Heath, Anne-Louise M., Lawrence, Julie, Galland, Barbara C., Gray, Andrew R., Taylor, Barry J., Sayers, Rachel, Taylor, Rachael W.“…The aims of this study were to determine how parenting style, infant temperament, and family type are associated with television viewing in two-year-old children. …”
Publicado 2017
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308por Cabacungan, Ashley N., Ellis, Matthew J., Sudan, Debra, Strigo, Tara S., Pounds, Iris, Riley, Jennie A., Falkovic, Margaret, Alkon, Aviel N., Peskoe, Sarah B., Davenport, Clemontina A., Pendergast, Jane F., Ephraim, Patti L., Mohottige, Dinushika, Diamantidis, Clarissa J., St. Clair Russell, Jennifer, DePasquale, Nicole, Boulware, L. Ebony“…We studied associations between perceived adequacy of live donor kidney transplant (LDKT) information or knowledge with pursuit of LDKT or receipt of live donor inquiries among 300 African American kidney transplant candidates. …”
Publicado 2020
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309por Chen, Junyu, Hui, Qin, Wang, Zeyuan, Wilson, Francis P., So-Armah, Kaku, Freiberg, Matthew S., Justice, Amy C., Xu, Ke, Zhao, Wei, Ammous, Farah, Smith, Jennifer A., Kardia, Sharon L.R., Gwinn, Marta, Marconi, Vincent C., Sun, Yan V.“…Replication was conducted among independent African American samples without HIV. RESULTS: DNA methylation sites cg17944885 near Zinc Finger Family Member 788 (ZNF788) and Zinc Finger Protein 20 (ZNF20), and cg06930757 in SHANK1 were significantly associated with eGFR among PWH of African ancestry (false discovery rate < 0.05). …”
Publicado 2023
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310“…Recent analysis revealing familial aggregation of arsenic metabolic profiles suggests that genetic factors could underlie interindividual variation in arsenic metabolism. …”
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311“…METHODS: In this study, we investigated the potential of FMO genes to confer risk of nicotine dependence via deep targeted sequencing in 2,820 study subjects comprising 1,583 nicotine dependents and 1,237 controls from European American and African American. Specifically, we focused on the two genomic segments including FMO1,FMO3, and pseudo gene FMO6P, and aimed to investigate the potential association between FMO genes and nicotine dependence. …”
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312por Iyengar, Sudha K., Sedor, John R., Freedman, Barry I., Kao, W. H. Linda, Kretzler, Matthias, Keller, Benjamin J., Abboud, Hanna E., Adler, Sharon G., Best, Lyle G., Bowden, Donald W., Burlock, Allison, Chen, Yii-Der Ida, Cole, Shelley A., Comeau, Mary E., Curtis, Jeffrey M., Divers, Jasmin, Drechsler, Christiane, Duggirala, Ravi, Elston, Robert C., Guo, Xiuqing, Huang, Huateng, Hoffmann, Michael Marcus, Howard, Barbara V., Ipp, Eli, Kimmel, Paul L., Klag, Michael J., Knowler, William C., Kohn, Orly F., Leak, Tennille S., Leehey, David J., Li, Man, Malhotra, Alka, März, Winfried, Nair, Viji, Nelson, Robert G., Nicholas, Susanne B., O’Brien, Stephen J., Pahl, Madeleine V., Parekh, Rulan S., Pezzolesi, Marcus G., Rasooly, Rebekah S., Rotimi, Charles N., Rotter, Jerome I., Schelling, Jeffrey R., Seldin, Michael F., Shah, Vallabh O., Smiles, Adam M., Smith, Michael W., Taylor, Kent D., Thameem, Farook, Thornley-Brown, Denyse P., Truitt, Barbara J., Wanner, Christoph, Weil, E. Jennifer, Winkler, Cheryl A., Zager, Philip G., Igo, Robert P., Hanson, Robert L., Langefeld, Carl D.“…The Family Investigation of Nephropathy and Diabetes (FIND) performed a genome-wide association study (GWAS) contrasting 6,197 unrelated individuals with advanced DKD with healthy and diabetic individuals lacking nephropathy of European American, African American, Mexican American, or American Indian ancestry. …”
Publicado 2015
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313por Mukhopadhyay, Nandita, Feingold, Eleanor, Moreno-Uribe, Lina, Wehby, George, Valencia-Ramirez, Luz Consuelo, Muñeton, Claudia P. Restrepo, Padilla, Carmencita, Deleyiannis, Frederic, Christensen, Kaare, Poletta, Fernando A., Orioli, Ieda M., Hecht, Jacqueline T., Buxó, Carmen J., Butali, Azeez, Adeyemo, Wasiu L., Vieira, Alexandre R., Shaffer, John R., Murray, Jeffrey C., Weinberg, Seth M., Leslie, Elizabeth J., Marazita, Mary L.“…In this current study, we analyzed 2,915 OFC cases, 6,044 unaffected individuals related to the OFC cases, and 2,685 controls with no personal or family history of OFC. Participants were grouped by their ancestry into African, Asian, European, and Central and South American subsets, and genome-wide association run on the combined sample as well as the four ancestry-based groups. …”
Publicado 2021
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314por Ward-Caviness, Cavin K., Neas, Lucas M., Blach, Colette, Haynes, Carol S., LaRocque-Abramson, Karen, Grass, Elizabeth, Dowdy, Elaine, Devlin, Robert B., Diaz-Sanchez, David, Cascio, Wayne E., Lynn Miranda, Marie, Gregory, Simon G., Shah, Svati H., Kraus, William E., Hauser, Elizabeth R.“…The rs755249-traffic exposure interaction was associated with PAD at a genome-wide significant level (P = 2.29x10(-8)) in European-Americans. …”
Publicado 2016
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316por Khan, Rumana J, Needham, Belinda L, Advani, Shailesh, Brown, Kristen, Dagnall, Casey, Xu, Ruihua, Gibbons, Gary H., Davis, Sharon K.“…We also assessed the mediating role of behavioral and psychosocial factors in the association between childhood SES and adult TL. METHODS: Childhood SES was assessed individually by using participant’s mother’s education and occupation, father’s education and occupation, parental home ownership, and family structure. …”
Publicado 2021
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319por Patel, Radhey, Arisoyin, Abimbola E, Okoronkwo, Obiaku U, Aruoture, Shaw, Okobi, Okelue E, Nwankwo, Mirian, Okobi, Emeka, Okobi, Francis, Momodu, Oshoriamhe ElishaEnlace del recurso
Publicado 2023
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320“…Building on previous work, we tested whether religious attendance was inversely associated with sleep disturbance among older Mexican Americans. …”
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