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Showing 1 to 12 of 22 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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AIRVF: a filtering toolbox for precise variant calling in Ion Torrent sequencing.

Bioinformatics (Oxford, England)

Shin S, Lee H, Son H, Paik S, Kim S.
PMID: 29126106
Bioinformatics. 2018 Apr 01;34(7):1232-1234. doi: 10.1093/bioinformatics/btx719.

SUMMARY: Ion Torrent sequencing is one of the most frequently used platforms in healthcare research and industry. Despite many advantages, platform-specific artifacts complicate efficient separation of true variants from errors, especially in variants with lower allele frequencies (

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Shin S, Lee H, Son H, et al. AIRVF: a filtering toolbox for precise variant calling in Ion Torrent sequencing. Bioinformatics. 2018;34(7):1232-1234doi: 10.1093/bioinformatics/btx719.
Shin, S., Lee, H., Son, H., Paik, S., & Kim, S. (2018). AIRVF: a filtering toolbox for precise variant calling in Ion Torrent sequencing. Bioinformatics (Oxford, England), 34(7), 1232-1234. https://doi.org/10.1093/bioinformatics/btx719
Shin, Sunguk, et al. "AIRVF: a filtering toolbox for precise variant calling in Ion Torrent sequencing." Bioinformatics (Oxford, England) vol. 34,7 (2018): 1232-1234. doi: https://doi.org/10.1093/bioinformatics/btx719
Shin S, Lee H, Son H, Paik S, Kim S. AIRVF: a filtering toolbox for precise variant calling in Ion Torrent sequencing. Bioinformatics. 2018 Apr 01;34(7):1232-1234. doi: 10.1093/bioinformatics/btx719. PMID: 29126106.
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Phenotypic spectrum of POLG1 mutations.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Finsterer J, Scorza FA.
PMID: 28905223
Neurol Sci. 2018 Mar;39(3):571-573. doi: 10.1007/s10072-017-3116-1. Epub 2017 Sep 13.

No abstract available.

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Finsterer J, Scorza FA. Phenotypic spectrum of POLG1 mutations. Neurol Sci. 2017;39(3):571-573doi: 10.1007/s10072-017-3116-1.
Finsterer, J., & Scorza, F. A. (2018). Phenotypic spectrum of POLG1 mutations. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 39(3), 571-573. https://doi.org/10.1007/s10072-017-3116-1
Finsterer, Josef, and Scorza, Fulvio A. "Phenotypic spectrum of POLG1 mutations." Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 39,3 (2018): 571-573. doi: https://doi.org/10.1007/s10072-017-3116-1
Finsterer J, Scorza FA. Phenotypic spectrum of POLG1 mutations. Neurol Sci. 2018 Mar;39(3):571-573. doi: 10.1007/s10072-017-3116-1. Epub 2017 Sep 13. PMID: 28905223.
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[Distribution of six STR loci in Bai ethnic group in Yunnan province of China].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Zou P, Yang Y, Li D, Zou L, Shen B.
PMID: 10359866
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 1999 Jun;16(3):160-3.

OBJECTIVE: This study was conducted to make known the distribution of six STR loci in Bai ethnic group in Yunnan province.METHODS: DAN extraction from blood samples (126 in number ) and multiplex amplification of CSF1PO,TPOX, TH01,F13A01, FESFPS and vWA...

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Zou P, Yang Y, Li D, et al. [Distribution of six STR loci in Bai ethnic group in Yunnan province of China]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 1999;16(3):160-3
Zou, P., Yang, Y., Li, D., Zou, L., & Shen, B. (1999). [Distribution of six STR loci in Bai ethnic group in Yunnan province of China]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 16(3), 160-3.
Zou, P, et al. "[Distribution of six STR loci in Bai ethnic group in Yunnan province of China]." Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 16,3 (1999): 160-3.
Zou P, Yang Y, Li D, Zou L, Shen B. [Distribution of six STR loci in Bai ethnic group in Yunnan province of China]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 1999 Jun;16(3):160-3. Chinese. PMID: 10359866.
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Gene-environment interactions--the BioBank UK study.

The pharmacogenomics journal

Wright AF, Carothers AD, Campbell H.
PMID: 12049178
Pharmacogenomics J. 2002;2(2):75-82. doi: 10.1038/sj.tpj.6500085.

No abstract available.

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Wright AF, Carothers AD, Campbell H. Gene-environment interactions--the BioBank UK study. Pharmacogenomics J. 2002;2(2):75-82doi: 10.1038/sj.tpj.6500085.
Wright, A. F., Carothers, A. D., & Campbell, H. (2002). Gene-environment interactions--the BioBank UK study. The pharmacogenomics journal, 2(2), 75-82. https://doi.org/10.1038/sj.tpj.6500085
Wright, A F, et al. "Gene-environment interactions--the BioBank UK study." The pharmacogenomics journal vol. 2,2 (2002): 75-82. doi: https://doi.org/10.1038/sj.tpj.6500085
Wright AF, Carothers AD, Campbell H. Gene-environment interactions--the BioBank UK study. Pharmacogenomics J. 2002;2(2):75-82. doi: 10.1038/sj.tpj.6500085. PMID: 12049178.
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Han Chinese population data for ten STR loci in Changsha, China.

Journal of forensic sciences

Ma Y, Gong B, Xia J, Deng H, Pan Q, Li Q, Dai H, Wen S, Xia K.
PMID: 11908620
J Forensic Sci. 2002 Mar;47(2):404-5.

No abstract available.

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Ma Y, Gong B, Xia J, et al. Han Chinese population data for ten STR loci in Changsha, China. J Forensic Sci. 2002;47(2):404-5
Ma, Y., Gong, B., Xia, J., Deng, H., Pan, Q., Li, Q., Dai, H., Wen, S., & Xia, K. (2002). Han Chinese population data for ten STR loci in Changsha, China. Journal of forensic sciences, 47(2), 404-5.
Ma, Yanlin, et al. "Han Chinese population data for ten STR loci in Changsha, China." Journal of forensic sciences vol. 47,2 (2002): 404-5.
Ma Y, Gong B, Xia J, Deng H, Pan Q, Li Q, Dai H, Wen S, Xia K. Han Chinese population data for ten STR loci in Changsha, China. J Forensic Sci. 2002 Mar;47(2):404-5. PMID: 11908620.
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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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POPDIST, version 1.1.1: a program to calculate population genetic distance and identity measures.

The Journal of heredity

Guldbrandtsen B, Tomiuk J, Loeschcke V.
PMID: 10768140
J Hered. 2000 Mar-Apr;91(2):178-9. doi: 10.1093/jhered/91.2.178.

No abstract available.

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Guldbrandtsen B, Tomiuk J, Loeschcke V. POPDIST, version 1.1.1: a program to calculate population genetic distance and identity measures. J Hered. 2000;91(2):178-9doi: 10.1093/jhered/91.2.178.
Guldbrandtsen, B., Tomiuk, J., & Loeschcke, V. (2000). POPDIST, version 1.1.1: a program to calculate population genetic distance and identity measures. The Journal of heredity, 91(2), 178-9. https://doi.org/10.1093/jhered/91.2.178
Guldbrandtsen, B, et al. "POPDIST, version 1.1.1: a program to calculate population genetic distance and identity measures." The Journal of heredity vol. 91,2 (2000): 178-9. doi: https://doi.org/10.1093/jhered/91.2.178
Guldbrandtsen B, Tomiuk J, Loeschcke V. POPDIST, version 1.1.1: a program to calculate population genetic distance and identity measures. J Hered. 2000 Mar-Apr;91(2):178-9. doi: 10.1093/jhered/91.2.178. PMID: 10768140.
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On the usage of HWE for identifying genotyping errors.

Annals of human genetics

Teo YY, Fry AE, Clark TG, Tai ES, Seielstad M.
PMID: 17388941
Ann Hum Genet. 2007 Sep;71:701-3; author reply 704. doi: 10.1111/j.1469-1809.2007.00356.x. Epub 2007 Mar 27.

No abstract available.

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Teo YY, Fry AE, Clark TG, et al. On the usage of HWE for identifying genotyping errors. Ann Hum Genet. 2007;71:701-3; author reply 704doi: 10.1111/j.1469-1809.2007.00356.x.
Teo, Y. Y., Fry, A. E., Clark, T. G., Tai, E. S., & Seielstad, M. (2007). On the usage of HWE for identifying genotyping errors. Annals of human genetics, 71701-3; author reply 704. https://doi.org/10.1111/j.1469-1809.2007.00356.x
Teo, Yik Y, et al. "On the usage of HWE for identifying genotyping errors." Annals of human genetics vol. 71 (2007): 701-3; author reply 704. doi: https://doi.org/10.1111/j.1469-1809.2007.00356.x
Teo YY, Fry AE, Clark TG, Tai ES, Seielstad M. On the usage of HWE for identifying genotyping errors. Ann Hum Genet. 2007 Sep;71:701-3; author reply 704. doi: 10.1111/j.1469-1809.2007.00356.x. Epub 2007 Mar 27. PMID: 17388941.
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Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

The American journal of gastroenterology

Hugot JP, Zaccaria I, Cavanaugh J, Yang H, Vermeire S, Lappalainen M, Schreiber S, Annese V, Jewell DP, Fowler EV, Brant SR, Silverberg MS, Cho J, Rioux JD, Satsangi J, Parkes M.
PMID: 17319929
Am J Gastroenterol. 2007 Jun;102(6):1259-67. doi: 10.1111/j.1572-0241.2007.01149.x. Epub 2007 Feb 23.

BACKGROUND: Crohn's disease (CD) has been associated with CARD15/NOD2 mutations in Caucasians. The R702W, G908R, and 1007fs mutations represent 82% of the mutated chromosomes. The relative risk of developing CD in homozygous or compound heterozygous people has been estimated...

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Hugot JP, Zaccaria I, Cavanaugh J, et al. Prevalence of CARD15/NOD2 mutations in Caucasian healthy people. Am J Gastroenterol. 2007;102(6):1259-67doi: 10.1111/j.1572-0241.2007.01149.x.
Hugot, J. P., Zaccaria, I., Cavanaugh, J., Yang, H., Vermeire, S., Lappalainen, M., Schreiber, S., Annese, V., Jewell, D. P., Fowler, E. V., Brant, S. R., Silverberg, M. S., Cho, J., Rioux, J. D., Satsangi, J., Parkes, M. (2007). Prevalence of CARD15/NOD2 mutations in Caucasian healthy people. The American journal of gastroenterology, 102(6), 1259-67. https://doi.org/10.1111/j.1572-0241.2007.01149.x
Hugot, Jean-Pierre, et al. "Prevalence of CARD15/NOD2 mutations in Caucasian healthy people." The American journal of gastroenterology vol. 102,6 (2007): 1259-67. doi: https://doi.org/10.1111/j.1572-0241.2007.01149.x
Hugot JP, Zaccaria I, Cavanaugh J, Yang H, Vermeire S, Lappalainen M, Schreiber S, Annese V, Jewell DP, Fowler EV, Brant SR, Silverberg MS, Cho J, Rioux JD, Satsangi J, Parkes M. Prevalence of CARD15/NOD2 mutations in Caucasian healthy people. Am J Gastroenterol. 2007 Jun;102(6):1259-67. doi: 10.1111/j.1572-0241.2007.01149.x. Epub 2007 Feb 23. PMID: 17319929.
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GWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample size.

Molecular psychiatry

Asif H, Alliey-Rodriguez N, Keedy S, Tamminga CA, Sweeney JA, Pearlson G, Clementz BA, Keshavan MS, Buckley P, Liu C, Neale B, Gershon ES.
PMID: 32066829
Mol Psychiatry. 2021 Jun;26(6):2048-2055. doi: 10.1038/s41380-020-0670-3. Epub 2020 Feb 17.

An important issue affecting genome-wide association studies with deep phenotyping (multiple correlated phenotypes) is determining the suitable family-wise significance threshold. Straightforward family-wise correction (Bonferroni) of p 

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Asif H, Alliey-Rodriguez N, Keedy S, et al. GWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample size. Mol Psychiatry. 2020;26(6):2048-2055doi: 10.1038/s41380-020-0670-3.
Asif, H., Alliey-Rodriguez, N., Keedy, S., Tamminga, C. A., Sweeney, J. A., Pearlson, G., Clementz, B. A., Keshavan, M. S., Buckley, P., Liu, C., Neale, B., & Gershon, E. S. (2021). GWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample size. Molecular psychiatry, 26(6), 2048-2055. https://doi.org/10.1038/s41380-020-0670-3
Asif, Huma, et al. "GWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample size." Molecular psychiatry vol. 26,6 (2021): 2048-2055. doi: https://doi.org/10.1038/s41380-020-0670-3
Asif H, Alliey-Rodriguez N, Keedy S, Tamminga CA, Sweeney JA, Pearlson G, Clementz BA, Keshavan MS, Buckley P, Liu C, Neale B, Gershon ES. GWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample size. Mol Psychiatry. 2021 Jun;26(6):2048-2055. doi: 10.1038/s41380-020-0670-3. Epub 2020 Feb 17. PMID: 32066829; PMCID: PMC7429341.
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The meaning of near-neutrality at coding and non-coding regions.

Gene

Ohta T.
PMID: 9461400
Gene. 1997 Dec 31;205(1):261-7. doi: 10.1016/s0378-1119(97)00396-x.

The nature of weak selection differs between coding and non-coding regions. Coding regions contain genetic information, whereas most non-coding regions do not have any information. Genetic information may be regarded as interaction systems, and the NK model of Kauffman...

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Ohta T. The meaning of near-neutrality at coding and non-coding regions. Gene. 1997;205(1):261-7doi: 10.1016/s0378-1119(97)00396-x.
Ohta, T. (1997). The meaning of near-neutrality at coding and non-coding regions. Gene, 205(1), 261-7. https://doi.org/10.1016/s0378-1119(97)00396-x
Ohta, T. "The meaning of near-neutrality at coding and non-coding regions." Gene vol. 205,1 (1997): 261-7. doi: https://doi.org/10.1016/s0378-1119(97)00396-x
Ohta T. The meaning of near-neutrality at coding and non-coding regions. Gene. 1997 Dec 31;205(1):261-7. doi: 10.1016/s0378-1119(97)00396-x. PMID: 9461400.
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Showing 1 to 12 of 22 entries