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Genetic and regulatory architecture of Alzheimer's disease in the .

Alzheimer's & dementia (Amsterdam, Netherlands)

Kulminski AM, Shu L, Loika Y, He L, Nazarian A, Arbeev K, Ukraintseva S, Yashin A, Culminskaya I.
PMID: 32211503
Alzheimers Dement (Amst). 2020 Feb 06;12(1):e12008. doi: 10.1002/dad2.12008. eCollection 2020.

INTRODUCTION: Apolipoprotein E (METHODS: We examined differences in linkage disequilibrium (LD) structures between (1) AD-affected and unaffected subjects and (2) older AD-unaffected and younger subjects in the 19q13.3 region harboring rs7412 and rs429358.RESULTS: AD is associated with sex-nonspecific heterogeneous...

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Kulminski AM, Shu L, Loika Y, et al. Genetic and regulatory architecture of Alzheimer's disease in the . Alzheimers Dement (Amst). 2020;12(1):e12008doi: 10.1002/dad2.12008.
Kulminski, A. M., Shu, L., Loika, Y., He, L., Nazarian, A., Arbeev, K., Ukraintseva, S., Yashin, A., & Culminskaya, I. (2020). Genetic and regulatory architecture of Alzheimer's disease in the . Alzheimer's & dementia (Amsterdam, Netherlands), 12(1), e12008. https://doi.org/10.1002/dad2.12008
Kulminski, Alexander M, et al. "Genetic and regulatory architecture of Alzheimer's disease in the ." Alzheimer's & dementia (Amsterdam, Netherlands) vol. 12,1 (2020): e12008. doi: https://doi.org/10.1002/dad2.12008
Kulminski AM, Shu L, Loika Y, He L, Nazarian A, Arbeev K, Ukraintseva S, Yashin A, Culminskaya I. Genetic and regulatory architecture of Alzheimer's disease in the . Alzheimers Dement (Amst). 2020 Feb 06;12(1):e12008. doi: 10.1002/dad2.12008. eCollection 2020. PMID: 32211503; PMCID: PMC7085286.
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Plasma Sphingomyelins in Late-Onset Alzheimer's Disease.

Journal of Alzheimer's disease : JAD

Fote G, Wu J, Mapstone M, Macciardi F, Fiandaca MS, Federoff HJ.
PMID: 34397408
J Alzheimers Dis. 2021;83(3):1161-1171. doi: 10.3233/JAD-200871.

BACKGROUND: Altered plasma levels of sphingolipids, including sphingomyelins (SM), have been found in mouse models of Alzheimer's disease (AD) and in AD patient plasma samples.OBJECTIVE: This study assesses fourteen plasma SM species in a late-onset AD (LOAD) patient cohort...

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Fote G, Wu J, Mapstone M, et al. Plasma Sphingomyelins in Late-Onset Alzheimer's Disease. J Alzheimers Dis. 2021;83(3):1161-1171doi: 10.3233/JAD-200871.
Fote, G., Wu, J., Mapstone, M., Macciardi, F., Fiandaca, M. S., & Federoff, H. J. (2021). Plasma Sphingomyelins in Late-Onset Alzheimer's Disease. Journal of Alzheimer's disease : JAD, 83(3), 1161-1171. https://doi.org/10.3233/JAD-200871
Fote, Gianna, et al. "Plasma Sphingomyelins in Late-Onset Alzheimer's Disease." Journal of Alzheimer's disease : JAD vol. 83,3 (2021): 1161-1171. doi: https://doi.org/10.3233/JAD-200871
Fote G, Wu J, Mapstone M, Macciardi F, Fiandaca MS, Federoff HJ. Plasma Sphingomyelins in Late-Onset Alzheimer's Disease. J Alzheimers Dis. 2021;83(3):1161-1171. doi: 10.3233/JAD-200871. PMID: 34397408.
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The Genetic Contribution of West-African Ancestry to Protection against Central Obesity in African-American Men but Not Women: Results from the ARIC and MESA Studies.

Frontiers in genetics

Klimentidis YC, Arora A, Zhou J, Kittles R, Allison DB.
PMID: 27313598
Front Genet. 2016 Jun 01;7:89. doi: 10.3389/fgene.2016.00089. eCollection 2016.

Over 80% of African-American (AA) women are overweight or obese. A large racial disparity between AA and European-Americans (EA) in obesity rates exists among women, but curiously not among men. Although socio-economic and/or cultural factors may partly account for...

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Klimentidis YC, Arora A, Zhou J, et al. The Genetic Contribution of West-African Ancestry to Protection against Central Obesity in African-American Men but Not Women: Results from the ARIC and MESA Studies. Front Genet. 2016;7:89doi: 10.3389/fgene.2016.00089.
Klimentidis, Y. C., Arora, A., Zhou, J., Kittles, R., & Allison, D. B. (2016). The Genetic Contribution of West-African Ancestry to Protection against Central Obesity in African-American Men but Not Women: Results from the ARIC and MESA Studies. Frontiers in genetics, 789. https://doi.org/10.3389/fgene.2016.00089
Klimentidis, Yann C, et al. "The Genetic Contribution of West-African Ancestry to Protection against Central Obesity in African-American Men but Not Women: Results from the ARIC and MESA Studies." Frontiers in genetics vol. 7 (2016): 89. doi: https://doi.org/10.3389/fgene.2016.00089
Klimentidis YC, Arora A, Zhou J, Kittles R, Allison DB. The Genetic Contribution of West-African Ancestry to Protection against Central Obesity in African-American Men but Not Women: Results from the ARIC and MESA Studies. Front Genet. 2016 Jun 01;7:89. doi: 10.3389/fgene.2016.00089. eCollection 2016. PMID: 27313598; PMCID: PMC4888933.
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Daily Activity Measured With Wearable Technology as a Novel Measurement of Treatment Effect in Patients With Coronary Microvascular Dysfunction: Substudy of a Randomized Controlled Crossover Trial.

JMIR research protocols

Birkeland K, Khandwalla RM, Kedan I, Shufelt CL, Mehta PK, Minissian MB, Wei J, Handberg EM, Thomson LE, Berman DS, Petersen JW, Anderson RD, Cook-Wiens G, Pepine CJ, Bairey Merz CN.
PMID: 29263019
JMIR Res Protoc. 2017 Dec 20;6(12):e255. doi: 10.2196/resprot.8057.

BACKGROUND: Digital wearable devices provide a "real-world" assessment of physical activity and quantify intervention-related changes in clinical trials. However, the value of digital wearable device-recorded physical activity as a clinical trial outcome is unknown.OBJECTIVE: Because late sodium channel inhibition...

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Birkeland K, Khandwalla RM, Kedan I, et al. Daily Activity Measured With Wearable Technology as a Novel Measurement of Treatment Effect in Patients With Coronary Microvascular Dysfunction: Substudy of a Randomized Controlled Crossover Trial. JMIR Res Protoc. 2017;6(12):e255doi: 10.2196/resprot.8057.
Birkeland, K., Khandwalla, R. M., Kedan, I., Shufelt, C. L., Mehta, P. K., Minissian, M. B., Wei, J., Handberg, E. M., Thomson, L. E., Berman, D. S., Petersen, J. W., Anderson, R. D., Cook-Wiens, G., Pepine, C. J., & Bairey Merz, C. N. (2017). Daily Activity Measured With Wearable Technology as a Novel Measurement of Treatment Effect in Patients With Coronary Microvascular Dysfunction: Substudy of a Randomized Controlled Crossover Trial. JMIR research protocols, 6(12), e255. https://doi.org/10.2196/resprot.8057
Birkeland, Kade, et al. "Daily Activity Measured With Wearable Technology as a Novel Measurement of Treatment Effect in Patients With Coronary Microvascular Dysfunction: Substudy of a Randomized Controlled Crossover Trial." JMIR research protocols vol. 6,12 (2017): e255. doi: https://doi.org/10.2196/resprot.8057
Birkeland K, Khandwalla RM, Kedan I, Shufelt CL, Mehta PK, Minissian MB, Wei J, Handberg EM, Thomson LE, Berman DS, Petersen JW, Anderson RD, Cook-Wiens G, Pepine CJ, Bairey Merz CN. Daily Activity Measured With Wearable Technology as a Novel Measurement of Treatment Effect in Patients With Coronary Microvascular Dysfunction: Substudy of a Randomized Controlled Crossover Trial. JMIR Res Protoc. 2017 Dec 20;6(12):e255. doi: 10.2196/resprot.8057. PMID: 29263019; PMCID: PMC5752966.
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Clonal hematopoiesis associated with epigenetic aging and clinical outcomes.

Aging cell

Nachun D, Lu AT, Bick AG, Natarajan P, Weinstock J, Szeto MD, Kathiresan S, Abecasis G, Taylor KD, Guo X, Tracy R, Durda P, Liu Y, Johnson C, Rich SS, Van Den Berg D, Laurie C, Blackwell T, Papanicolaou GJ, Correa A, Raffield LM, Johnson AD, Murabito J, Manson JE, Desai P, Kooperberg C, Assimes TL, Levy D, Rotter JI, Reiner AP, Whitsel EA, Wilson JG, Horvath S, Jaiswal S.
PMID: 34050697
Aging Cell. 2021 Jun;20(6):e13366. doi: 10.1111/acel.13366. Epub 2021 May 29.

Clonal hematopoiesis of indeterminate potential (CHIP) is a common precursor state for blood cancers that most frequently occurs due to mutations in the DNA-methylation modifying enzymes DNMT3A or TET2. We used DNA-methylation array and whole-genome sequencing data from four...

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Nachun D, Lu AT, Bick AG, et al. Clonal hematopoiesis associated with epigenetic aging and clinical outcomes. Aging Cell. 2021;20(6):e13366doi: 10.1111/acel.13366.
Nachun, D., Lu, A. T., Bick, A. G., Natarajan, P., Weinstock, J., Szeto, M. D., Kathiresan, S., Abecasis, G., Taylor, K. D., Guo, X., Tracy, R., Durda, P., Liu, Y., Johnson, C., Rich, S. S., Van Den Berg, D., Laurie, C., Blackwell, T., Papanicolaou, G. J., Correa, A., Raffield, L. M., Johnson, A. D., Murabito, J., Manson, J. E., Desai, P., Kooperberg, C., Assimes, T. L., Levy, D., Rotter, J. I., Reiner, A. P., Whitsel, E. A., Wilson, J. G., Horvath, S., Jaiswal, S. (2021). Clonal hematopoiesis associated with epigenetic aging and clinical outcomes. Aging cell, 20(6), e13366. https://doi.org/10.1111/acel.13366
Nachun, Daniel, et al. "Clonal hematopoiesis associated with epigenetic aging and clinical outcomes." Aging cell vol. 20,6 (2021): e13366. doi: https://doi.org/10.1111/acel.13366
Nachun D, Lu AT, Bick AG, Natarajan P, Weinstock J, Szeto MD, Kathiresan S, Abecasis G, Taylor KD, Guo X, Tracy R, Durda P, Liu Y, Johnson C, Rich SS, Van Den Berg D, Laurie C, Blackwell T, Papanicolaou GJ, Correa A, Raffield LM, Johnson AD, Murabito J, Manson JE, Desai P, Kooperberg C, Assimes TL, Levy D, Rotter JI, Reiner AP, Whitsel EA, Wilson JG, Horvath S, Jaiswal S. Clonal hematopoiesis associated with epigenetic aging and clinical outcomes. Aging Cell. 2021 Jun;20(6):e13366. doi: 10.1111/acel.13366. Epub 2021 May 29. PMID: 34050697; PMCID: PMC8208788.
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Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function.

Scientific reports

Yang T, Jackson VE, Smith AV, Chen H, Bartz TM, Sitlani CM, Psaty BM, Gharib SA, O'Connor GT, Dupuis J, Xu J, Lohman K, Liu Y, Kritchevsky SB, Cassano PA, Flexeder C, Gieger C, Karrasch S, Peters A, Schulz H, Harris SE, Starr JM, Deary IJ, Manichaikul A, Oelsner EC, Barr RG, Taylor KD, Rich SS, Bonten TN, Mook-Kanamori DO, Noordam R, Li-Gao R, Jarvelin MR, Wielscher M, Terzikhan N, Lahousse L, Brusselle G, Weiss S, Ewert R, Gläser S, Homuth G, Shrine N, Hall IP, Tobin M, London SJ, Wei P, Morrison AC.
PMID: 34588469
Sci Rep. 2021 Sep 29;11(1):19365. doi: 10.1038/s41598-021-98120-7.

Genome-wide association studies have identified numerous common genetic variants associated with spirometric measures of pulmonary function, including forced expiratory volume in one second (FEV

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Yang T, Jackson VE, Smith AV, et al. Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function. Sci Rep. 2021;11(1):19365doi: 10.1038/s41598-021-98120-7.
Yang, T., Jackson, V. E., Smith, A. V., Chen, H., Bartz, T. M., Sitlani, C. M., Psaty, B. M., Gharib, S. A., O'Connor, G. T., Dupuis, J., Xu, J., Lohman, K., Liu, Y., Kritchevsky, S. B., Cassano, P. A., Flexeder, C., Gieger, C., Karrasch, S., Peters, A., Schulz, H., Harris, S. E., Starr, J. M., Deary, I. J., Manichaikul, A., Oelsner, E. C., Barr, R. G., Taylor, K. D., Rich, S. S., Bonten, T. N., Mook-Kanamori, D. O., Noordam, R., Li-Gao, R., Jarvelin, M. R., Wielscher, M., Terzikhan, N., Lahousse, L., Brusselle, G., Weiss, S., Ewert, R., Gläser, S., Homuth, G., Shrine, N., Hall, I. P., Tobin, M., London, S. J., Wei, P., & Morrison, A. C. (2021). Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function. Scientific reports, 11(1), 19365. https://doi.org/10.1038/s41598-021-98120-7
Yang, Tianzhong, et al. "Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function." Scientific reports vol. 11,1 (2021): 19365. doi: https://doi.org/10.1038/s41598-021-98120-7
Yang T, Jackson VE, Smith AV, Chen H, Bartz TM, Sitlani CM, Psaty BM, Gharib SA, O'Connor GT, Dupuis J, Xu J, Lohman K, Liu Y, Kritchevsky SB, Cassano PA, Flexeder C, Gieger C, Karrasch S, Peters A, Schulz H, Harris SE, Starr JM, Deary IJ, Manichaikul A, Oelsner EC, Barr RG, Taylor KD, Rich SS, Bonten TN, Mook-Kanamori DO, Noordam R, Li-Gao R, Jarvelin MR, Wielscher M, Terzikhan N, Lahousse L, Brusselle G, Weiss S, Ewert R, Gläser S, Homuth G, Shrine N, Hall IP, Tobin M, London SJ, Wei P, Morrison AC. Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function. Sci Rep. 2021 Sep 29;11(1):19365. doi: 10.1038/s41598-021-98120-7. PMID: 34588469; PMCID: PMC8481467.
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Showing 25 to 30 of 30 entries