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Showing 1 to 12 of 28 entries
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Uralic genes in Europe.

American journal of physical anthropology

Guglielmino CR, Piazza A, Menozzi P, Cavalli-Sforza LL.
PMID: 2221031
Am J Phys Anthropol. 1990 Sep;83(1):57-68. doi: 10.1002/ajpa.1330830107.

We have analysed data of three European populations speaking non-Indoeuropean languages: Hungarians, Lapps, and Finns. Principal coordinate analysis shows that Lapps are almost exactly intermediate between people located geographically near the Ural mountains and speaking Uralic languages, and central...

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Guglielmino CR, Piazza A, Menozzi P, et al. Uralic genes in Europe. Am J Phys Anthropol. 1990;83(1):57-68doi: 10.1002/ajpa.1330830107.
Guglielmino, C. R., Piazza, A., Menozzi, P., & Cavalli-Sforza, L. L. (1990). Uralic genes in Europe. American journal of physical anthropology, 83(1), 57-68. https://doi.org/10.1002/ajpa.1330830107
Guglielmino, C R, et al. "Uralic genes in Europe." American journal of physical anthropology vol. 83,1 (1990): 57-68. doi: https://doi.org/10.1002/ajpa.1330830107
Guglielmino CR, Piazza A, Menozzi P, Cavalli-Sforza LL. Uralic genes in Europe. Am J Phys Anthropol. 1990 Sep;83(1):57-68. doi: 10.1002/ajpa.1330830107. PMID: 2221031.
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Distribution of allele frequencies for two short tandem repeats (HUMTH01 and F13A01) among five Indian population groups.

Journal of forensic sciences

Ghosh A, Seshadri M.
PMID: 11908625
J Forensic Sci. 2002 Mar;47(2):415-6.

No abstract available.

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Ghosh A, Seshadri M. Distribution of allele frequencies for two short tandem repeats (HUMTH01 and F13A01) among five Indian population groups. J Forensic Sci. 2002;47(2):415-6
Ghosh, A., & Seshadri, M. (2002). Distribution of allele frequencies for two short tandem repeats (HUMTH01 and F13A01) among five Indian population groups. Journal of forensic sciences, 47(2), 415-6.
Ghosh, Anu, and Seshadri, M. "Distribution of allele frequencies for two short tandem repeats (HUMTH01 and F13A01) among five Indian population groups." Journal of forensic sciences vol. 47,2 (2002): 415-6.
Ghosh A, Seshadri M. Distribution of allele frequencies for two short tandem repeats (HUMTH01 and F13A01) among five Indian population groups. J Forensic Sci. 2002 Mar;47(2):415-6. PMID: 11908625.
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Pharmaceutical futures: made in China?.

Nature

Cyranoski D.
PMID: 18971994
Nature. 2008 Oct 30;455(7217):1168-70. doi: 10.1038/4551168a.

No abstract available.

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Cyranoski D. Pharmaceutical futures: made in China?. Nature. 2008;455(7217):1168-70doi: 10.1038/4551168a.
Cyranoski, D. (2008). Pharmaceutical futures: made in China?. Nature, 455(7217), 1168-70. https://doi.org/10.1038/4551168a
Cyranoski, David. "Pharmaceutical futures: made in China?." Nature vol. 455,7217 (2008): 1168-70. doi: https://doi.org/10.1038/4551168a
Cyranoski D. Pharmaceutical futures: made in China?. Nature. 2008 Oct 30;455(7217):1168-70. doi: 10.1038/4551168a. PMID: 18971994.
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Confirmation of novel type 1 diabetes risk loci in families.

Diabetologia

Cooper JD, Howson JM, Smyth D, Walker NM, Stevens H, Yang JH, She JX, Eisenbarth GS, Rewers M, Todd JA, Akolkar B, Concannon P, Erlich HA, Julier C, Morahan G, Nerup J, Nierras C, Pociot F, Rich SS.
PMID: 22278338
Diabetologia. 2012 Apr;55(4):996-1000. doi: 10.1007/s00125-012-2450-3. Epub 2012 Jan 26.

AIMS/HYPOTHESIS: Over 50 regions of the genome have been associated with type 1 diabetes risk, mainly using large case/control collections. In a recent genome-wide association (GWA) study, 18 novel susceptibility loci were identified and replicated, including replication evidence from...

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Cooper JD, Howson JM, Smyth D, et al. Confirmation of novel type 1 diabetes risk loci in families. Diabetologia. 2012;55(4):996-1000doi: 10.1007/s00125-012-2450-3.
Cooper, J. D., Howson, J. M., Smyth, D., Walker, N. M., Stevens, H., Yang, J. H., She, J. X., Eisenbarth, G. S., Rewers, M., Todd, J. A., Akolkar, B., Concannon, P., Erlich, H. A., Julier, C., Morahan, G., Nerup, J., Nierras, C., Pociot, F., Rich, S. S. (2012). Confirmation of novel type 1 diabetes risk loci in families. Diabetologia, 55(4), 996-1000. https://doi.org/10.1007/s00125-012-2450-3
Cooper, J D, et al. "Confirmation of novel type 1 diabetes risk loci in families." Diabetologia vol. 55,4 (2012): 996-1000. doi: https://doi.org/10.1007/s00125-012-2450-3
Cooper JD, Howson JM, Smyth D, Walker NM, Stevens H, Yang JH, She JX, Eisenbarth GS, Rewers M, Todd JA, Akolkar B, Concannon P, Erlich HA, Julier C, Morahan G, Nerup J, Nierras C, Pociot F, Rich SS. Confirmation of novel type 1 diabetes risk loci in families. Diabetologia. 2012 Apr;55(4):996-1000. doi: 10.1007/s00125-012-2450-3. Epub 2012 Jan 26. PMID: 22278338; PMCID: PMC3296014.
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Performance of genotype imputations using data from the 1000 Genomes Project.

Human heredity

Sung YJ, Wang L, Rankinen T, Bouchard C, Rao DC.
PMID: 22212296
Hum Hered. 2012;73(1):18-25. doi: 10.1159/000334084. Epub 2011 Dec 30.

Genotype imputations based on 1000 Genomes (1KG) Project data have the advantage of imputing many more SNPs than imputations based on HapMap data. It also provides an opportunity to discover associations with relatively rare variants. Recent investigations are increasingly...

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Sung YJ, Wang L, Rankinen T, et al. Performance of genotype imputations using data from the 1000 Genomes Project. Hum Hered. 2011;73(1):18-25doi: 10.1159/000334084.
Sung, Y. J., Wang, L., Rankinen, T., Bouchard, C., & Rao, D. C. (2012). Performance of genotype imputations using data from the 1000 Genomes Project. Human heredity, 73(1), 18-25. https://doi.org/10.1159/000334084
Sung, Yun Ju, et al. "Performance of genotype imputations using data from the 1000 Genomes Project." Human heredity vol. 73,1 (2012): 18-25. doi: https://doi.org/10.1159/000334084
Sung YJ, Wang L, Rankinen T, Bouchard C, Rao DC. Performance of genotype imputations using data from the 1000 Genomes Project. Hum Hered. 2012;73(1):18-25. doi: 10.1159/000334084. Epub 2011 Dec 30. PMID: 22212296; PMCID: PMC3322630.
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["Caucasian" you say?].

Annales de dermatologie et de venereologie

Penso-Assathiany D.
PMID: 24090887
Ann Dermatol Venereol. 2013 Oct;140(10):587-8. doi: 10.1016/j.annder.2013.07.016. Epub 2013 Aug 14.

No abstract available.

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Penso-Assathiany D. Vous avez dit caucasien ? ["Caucasian" you say?]. Ann Dermatol Venereol. 2013;140(10):587-8doi: 10.1016/j.annder.2013.07.016.
Penso-Assathiany, D. (2013). Vous avez dit caucasien ? ["Caucasian" you say?]. Annales de dermatologie et de venereologie, 140(10), 587-8. https://doi.org/10.1016/j.annder.2013.07.016
Penso-Assathiany, D. "Vous avez dit caucasien ?" ["Caucasian" you say?]. Annales de dermatologie et de venereologie vol. 140,10 (2013): 587-8. doi: https://doi.org/10.1016/j.annder.2013.07.016
Penso-Assathiany D. Vous avez dit caucasien ? ["Caucasian" you say?]. Ann Dermatol Venereol. 2013 Oct;140(10):587-8. doi: 10.1016/j.annder.2013.07.016. Epub 2013 Aug 14. French. PMID: 24090887.
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Simple and cost-effective 14-loci SNP assay designed for differentiation of European, East Asian and African samples.

Forensic science international. Genetics

Rogalla U, Rychlicka E, Derenko MV, Malyarchuk BA, Grzybowski T.
PMID: 25286442
Forensic Sci Int Genet. 2015 Jan;14:42-9. doi: 10.1016/j.fsigen.2014.09.009. Epub 2014 Sep 28.

During every criminal investigation, it is vital to extract as much information as possible from every piece of evidence. When it comes to DNA testing, simple short tandem repeat (STR) typing may soon become a relic because it is...

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Rogalla U, Rychlicka E, Derenko MV, et al. Simple and cost-effective 14-loci SNP assay designed for differentiation of European, East Asian and African samples. Forensic Sci Int Genet. 2014;14:42-9doi: 10.1016/j.fsigen.2014.09.009.
Rogalla, U., Rychlicka, E., Derenko, M. V., Malyarchuk, B. A., & Grzybowski, T. (2015). Simple and cost-effective 14-loci SNP assay designed for differentiation of European, East Asian and African samples. Forensic science international. Genetics, 1442-9. https://doi.org/10.1016/j.fsigen.2014.09.009
Rogalla, Urszula, et al. "Simple and cost-effective 14-loci SNP assay designed for differentiation of European, East Asian and African samples." Forensic science international. Genetics vol. 14 (2015): 42-9. doi: https://doi.org/10.1016/j.fsigen.2014.09.009
Rogalla U, Rychlicka E, Derenko MV, Malyarchuk BA, Grzybowski T. Simple and cost-effective 14-loci SNP assay designed for differentiation of European, East Asian and African samples. Forensic Sci Int Genet. 2015 Jan;14:42-9. doi: 10.1016/j.fsigen.2014.09.009. Epub 2014 Sep 28. PMID: 25286442.
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The promise and pitfalls of precision medicine to resolve black-white racial disparities in preterm birth.

Pediatric research

Burris HH, Wright CJ, Kirpalani H, Collins JW, Lorch SA, Elovitz MA, Hwang SS.
PMID: 31382269
Pediatr Res. 2020 Jan;87(2):221-226. doi: 10.1038/s41390-019-0528-z. Epub 2019 Aug 05.

Differences in preterm birth rates between black and white women are the largest contributor to racial disparities in infant mortality. In today's age of precision medicine, analysis of the genome, epigenome, metabolome, and microbiome has generated interest in determining...

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Burris HH, Wright CJ, Kirpalani H, et al. The promise and pitfalls of precision medicine to resolve black-white racial disparities in preterm birth. Pediatr Res. 2019;87(2):221-226doi: 10.1038/s41390-019-0528-z.
Burris, H. H., Wright, C. J., Kirpalani, H., Collins, J. W., Lorch, S. A., Elovitz, M. A., & Hwang, S. S. (2020). The promise and pitfalls of precision medicine to resolve black-white racial disparities in preterm birth. Pediatric research, 87(2), 221-226. https://doi.org/10.1038/s41390-019-0528-z
Burris, Heather H, et al. "The promise and pitfalls of precision medicine to resolve black-white racial disparities in preterm birth." Pediatric research vol. 87,2 (2020): 221-226. doi: https://doi.org/10.1038/s41390-019-0528-z
Burris HH, Wright CJ, Kirpalani H, Collins JW, Lorch SA, Elovitz MA, Hwang SS. The promise and pitfalls of precision medicine to resolve black-white racial disparities in preterm birth. Pediatr Res. 2020 Jan;87(2):221-226. doi: 10.1038/s41390-019-0528-z. Epub 2019 Aug 05. PMID: 31382269.
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Lifestyle for the prevention of type 2 diabetes: what is the role of genetic risk information?.

The American journal of clinical nutrition

Chen GC, Qi Q.
PMID: 31974545
Am J Clin Nutr. 2020 Mar 01;111(3):491-492. doi: 10.1093/ajcn/nqz350.

No abstract available.

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Chen GC, Qi Q. Lifestyle for the prevention of type 2 diabetes: what is the role of genetic risk information?. Am J Clin Nutr. 2020;111(3):491-492doi: 10.1093/ajcn/nqz350.
Chen, G. C., & Qi, Q. (2020). Lifestyle for the prevention of type 2 diabetes: what is the role of genetic risk information?. The American journal of clinical nutrition, 111(3), 491-492. https://doi.org/10.1093/ajcn/nqz350
Chen, Guo-Chong, and Qi, Qibin. "Lifestyle for the prevention of type 2 diabetes: what is the role of genetic risk information?." The American journal of clinical nutrition vol. 111,3 (2020): 491-492. doi: https://doi.org/10.1093/ajcn/nqz350
Chen GC, Qi Q. Lifestyle for the prevention of type 2 diabetes: what is the role of genetic risk information?. Am J Clin Nutr. 2020 Mar 01;111(3):491-492. doi: 10.1093/ajcn/nqz350. PMID: 31974545; PMCID: PMC7049531.
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Polygenic Scores for Height in Admixed Populations.

G3 (Bethesda, Md.)

Bitarello BD, Mathieson I.
PMID: 32878958
G3 (Bethesda). 2020 Nov 05;10(11):4027-4036. doi: 10.1534/g3.120.401658.

Polygenic risk scores (PRS) use the results of genome-wide association studies (GWAS) to predict quantitative phenotypes or disease risk at an individual level, and provide a potential route to the use of genetic data in personalized medical care. However,...

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Bitarello BD, Mathieson I. Polygenic Scores for Height in Admixed Populations. G3 (Bethesda). 2020;10(11):4027-4036doi: 10.1534/g3.120.401658.
Bitarello, B. D., & Mathieson, I. (2020). Polygenic Scores for Height in Admixed Populations. G3 (Bethesda, Md.), 10(11), 4027-4036. https://doi.org/10.1534/g3.120.401658
Bitarello, Bárbara D, and Mathieson, Iain. "Polygenic Scores for Height in Admixed Populations." G3 (Bethesda, Md.) vol. 10,11 (2020): 4027-4036. doi: https://doi.org/10.1534/g3.120.401658
Bitarello BD, Mathieson I. Polygenic Scores for Height in Admixed Populations. G3 (Bethesda). 2020 Nov 05;10(11):4027-4036. doi: 10.1534/g3.120.401658. PMID: 32878958; PMCID: PMC7642950.
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Genome-Wide Association of CKD Progression: The Chronic Renal Insufficiency Cohort Study.

Journal of the American Society of Nephrology : JASN

Parsa A, Kanetsky PA, Xiao R, Gupta J, Mitra N, Limou S, Xie D, Xu H, Anderson AH, Ojo A, Kusek JW, Lora CM, Hamm LL, He J, Sandholm N, Jeff J, Raj DE, Böger CA, Bottinger E, Salimi S, Parekh RS, Adler SG, Langefeld CD, Bowden DW, Groop PH, Forsblom C, Freedman BI, Lipkowitz M, Fox CS, Winkler CA, Feldman HI.
PMID: 27729571
J Am Soc Nephrol. 2017 Mar;28(3):923-934. doi: 10.1681/ASN.2015101152. Epub 2016 Oct 11.

The rate of decline of renal function varies significantly among individuals with CKD. To understand better the contribution of genetics to CKD progression, we performed a genome-wide association study among participants in the Chronic Renal Insufficiency Cohort Study. Our...

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Parsa A, Kanetsky PA, Xiao R, et al. Genome-Wide Association of CKD Progression: The Chronic Renal Insufficiency Cohort Study. J Am Soc Nephrol. 2016;28(3):923-934doi: 10.1681/ASN.2015101152.
Parsa, A., Kanetsky, P. A., Xiao, R., Gupta, J., Mitra, N., Limou, S., Xie, D., Xu, H., Anderson, A. H., Ojo, A., Kusek, J. W., Lora, C. M., Hamm, L. L., He, J., Sandholm, N., Jeff, J., Raj, D. E., Böger, C. A., Bottinger, E., Salimi, S., Parekh, R. S., Adler, S. G., Langefeld, C. D., Bowden, D. W., Groop, P. H., Forsblom, C., Freedman, B. I., Lipkowitz, M., Fox, C. S., Winkler, C. A., Feldman, H. I. (2017). Genome-Wide Association of CKD Progression: The Chronic Renal Insufficiency Cohort Study. Journal of the American Society of Nephrology : JASN, 28(3), 923-934. https://doi.org/10.1681/ASN.2015101152
Parsa, Afshin, et al. "Genome-Wide Association of CKD Progression: The Chronic Renal Insufficiency Cohort Study." Journal of the American Society of Nephrology : JASN vol. 28,3 (2017): 923-934. doi: https://doi.org/10.1681/ASN.2015101152
Parsa A, Kanetsky PA, Xiao R, Gupta J, Mitra N, Limou S, Xie D, Xu H, Anderson AH, Ojo A, Kusek JW, Lora CM, Hamm LL, He J, Sandholm N, Jeff J, Raj DE, Böger CA, Bottinger E, Salimi S, Parekh RS, Adler SG, Langefeld CD, Bowden DW, Groop PH, Forsblom C, Freedman BI, Lipkowitz M, Fox CS, Winkler CA, Feldman HI. Genome-Wide Association of CKD Progression: The Chronic Renal Insufficiency Cohort Study. J Am Soc Nephrol. 2017 Mar;28(3):923-934. doi: 10.1681/ASN.2015101152. Epub 2016 Oct 11. PMID: 27729571; PMCID: PMC5328149.
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Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array.

Genomics

Hoffmann TJ, Kvale MN, Hesselson SE, Zhan Y, Aquino C, Cao Y, Cawley S, Chung E, Connell S, Eshragh J, Ewing M, Gollub J, Henderson M, Hubbell E, Iribarren C, Kaufman J, Lao RZ, Lu Y, Ludwig D, Mathauda GK, McGuire W, Mei G, Miles S, Purdy MM, Quesenberry C, Ranatunga D, Rowell S, Sadler M, Shapero MH, Shen L, Shenoy TR, Smethurst D, Van den Eeden SK, Walter L, Wan E, Wearley R, Webster T, Wen CC, Weng L, Whitmer RA, Williams A, Wong SC, Zau C, Finn A, Schaefer C, Kwok PY, Risch N.
PMID: 21565264
Genomics. 2011 Aug;98(2):79-89. doi: 10.1016/j.ygeno.2011.04.005. Epub 2011 Apr 30.

The success of genome-wide association studies has paralleled the development of efficient genotyping technologies. We describe the development of a next-generation microarray based on the new highly-efficient Affymetrix Axiom genotyping technology that we are using to genotype individuals of...

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Hoffmann TJ, Kvale MN, Hesselson SE, et al. Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array. Genomics. 2011;98(2):79-89doi: 10.1016/j.ygeno.2011.04.005.
Hoffmann, T. J., Kvale, M. N., Hesselson, S. E., Zhan, Y., Aquino, C., Cao, Y., Cawley, S., Chung, E., Connell, S., Eshragh, J., Ewing, M., Gollub, J., Henderson, M., Hubbell, E., Iribarren, C., Kaufman, J., Lao, R. Z., Lu, Y., Ludwig, D., Mathauda, G. K., McGuire, W., Mei, G., Miles, S., Purdy, M. M., Quesenberry, C., Ranatunga, D., Rowell, S., Sadler, M., Shapero, M. H., Shen, L., Shenoy, T. R., Smethurst, D., Van den Eeden, S. K., Walter, L., Wan, E., Wearley, R., Webster, T., Wen, C. C., Weng, L., Whitmer, R. A., Williams, A., Wong, S. C., Zau, C., Finn, A., Schaefer, C., Kwok, P. Y., & Risch, N. (2011). Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array. Genomics, 98(2), 79-89. https://doi.org/10.1016/j.ygeno.2011.04.005
Hoffmann, Thomas J, et al. "Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array." Genomics vol. 98,2 (2011): 79-89. doi: https://doi.org/10.1016/j.ygeno.2011.04.005
Hoffmann TJ, Kvale MN, Hesselson SE, Zhan Y, Aquino C, Cao Y, Cawley S, Chung E, Connell S, Eshragh J, Ewing M, Gollub J, Henderson M, Hubbell E, Iribarren C, Kaufman J, Lao RZ, Lu Y, Ludwig D, Mathauda GK, McGuire W, Mei G, Miles S, Purdy MM, Quesenberry C, Ranatunga D, Rowell S, Sadler M, Shapero MH, Shen L, Shenoy TR, Smethurst D, Van den Eeden SK, Walter L, Wan E, Wearley R, Webster T, Wen CC, Weng L, Whitmer RA, Williams A, Wong SC, Zau C, Finn A, Schaefer C, Kwok PY, Risch N. Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array. Genomics. 2011 Aug;98(2):79-89. doi: 10.1016/j.ygeno.2011.04.005. Epub 2011 Apr 30. PMID: 21565264; PMCID: PMC3146553.
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Showing 1 to 12 of 28 entries