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Items: 1 to 20 of 2962

1.

The Empirical Distribution of Singletons for Geographic Samples of DNA Sequences.

Cubry P, Vigouroux Y, François O.

Front Genet. 2017 Sep 29;8:139. doi: 10.3389/fgene.2017.00139. eCollection 2017.

2.

Regional variation in health is predominantly driven by lifestyle rather than genetics.

Amador C, Xia C, Nagy R, Campbell A, Porteous D, Smith BH, Hastie N, Vitart V, Hayward C, Navarro P, Haley CS.

Nat Commun. 2017 Oct 6;8(1):801. doi: 10.1038/s41467-017-00497-5.

3.

STRScan: targeted profiling of short tandem repeats in whole-genome sequencing data.

Tang H, Nzabarushimana E.

BMC Bioinformatics. 2017 Oct 3;18(Suppl 11):398. doi: 10.1186/s12859-017-1800-z.

4.

Genetic Analysis of Mitochondrial Ribosomal Proteins and Cognitive Aging in Postmenopausal Women.

Mozhui K, Snively BM, Rapp SR, Wallace RB, Williams RW, Johnson KC.

Front Genet. 2017 Sep 21;8:127. doi: 10.3389/fgene.2017.00127. eCollection 2017.

5.

A Histidine pH sensor regulates activation of the Ras-specific guanine nucleotide exchange factor RasGRP1.

Vercoulen Y, Kondo Y, Iwig JS, Janssen AB, White KA, Amini M, Barber DL, Kuriyan J, Roose JP.

Elife. 2017 Sep 27;6. pii: e29002. doi: 10.7554/eLife.29002.

6.

Spatial distribution of disease-associated variants in three-dimensional structures of protein complexes.

Gress A, Ramensky V, Kalinina OV.

Oncogenesis. 2017 Sep 25;6(9):e380. doi: 10.1038/oncsis.2017.79.

7.

Assessing risk for Mendelian disorders in a Bronx population.

diSibio G, Upadhyay K, Meyer P, Oddoux C, Ostrer H.

Mol Genet Genomic Med. 2017 Jul 6;5(5):516-523. doi: 10.1002/mgg3.307. eCollection 2017 Sep.

8.

Deep whole-genome sequencing of 90 Han Chinese genomes.

Lan T, Lin H, Zhu W, Laurent TCAM, Yang M, Liu X, Wang J, Wang J, Yang H, Xu X, Guo X.

Gigascience. 2017 Sep 1;6(9):1-7. doi: 10.1093/gigascience/gix067.

9.

XCAVATOR: accurate detection and genotyping of copy number variants from second and third generation whole-genome sequencing experiments.

Magi A, Pippucci T, Sidore C.

BMC Genomics. 2017 Sep 21;18(1):747. doi: 10.1186/s12864-017-4137-0.

10.

Using sheep genomes from diverse U.S. breeds to identify missense variants in genes affecting fecundity.

Heaton MP, Smith TPL, Freking BA, Workman AM, Bennett GL, Carnahan JK, Kalbfleisch TS.

F1000Res. 2017 Aug 2;6:1303. doi: 10.12688/f1000research.12216.1. eCollection 2017.

11.

Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.

Tian C, Hromatka BS, Kiefer AK, Eriksson N, Noble SM, Tung JY, Hinds DA.

Nat Commun. 2017 Sep 19;8(1):599. doi: 10.1038/s41467-017-00257-5.

12.

Population-specific genetic variation in large sequencing data sets: why more data is still better.

van Rooij JGJ, Jhamai M, Arp PP, Nouwens SCA, Verkerk M, Hofman A, Ikram MA, Verkerk AJ, van Meurs JBJ, Rivadeneira F, Uitterlinden AG, Kraaij R.

Eur J Hum Genet. 2017 Oct;25(10):1173-1175. doi: 10.1038/ejhg.2017.110. Epub 2017 Jul 19.

PMID:
28905877
13.

Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism.

Li N, Johnson DC, Weinhold N, Kimber S, Dobbins SE, Mitchell JS, Kinnersley B, Sud A, Law PJ, Orlando G, Scales M, Wardell CP, Försti A, Hoang PH, Went M, Holroyd A, Hariri F, Pastinen T, Meissner T, Goldschmidt H, Hemminki K, Morgan GJ, Kaiser M, Houlston RS.

Cell Rep. 2017 Sep 12;20(11):2556-2564. doi: 10.1016/j.celrep.2017.08.062.

14.

A Bayesian test for Hardy-Weinberg equilibrium of biallelic X-chromosomal markers.

Puig X, Ginebra J, Graffelman J.

Heredity (Edinb). 2017 Oct;119(4):226-236. doi: 10.1038/hdy.2017.30. Epub 2017 Jul 5.

15.

Haplotype dependent association of rs7927894 (11q13.5) with atopic dermatitis and chronic allergic rhinitis: A study in ECAP cohort.

Ponińska JK, Samoliński B, Tomaszewska A, Raciborski F, Samel-Kowalik P, Walkiewicz A, Lipiec A, Piekarska B, Krzych-Fałta E, Namysłowski A, Kostrzewa G, Pawlik A, Jasek M, Wiśniewski A, Kuśnierczyk P, Majewski S, Płoski R.

PLoS One. 2017 Sep 8;12(9):e0183922. doi: 10.1371/journal.pone.0183922. eCollection 2017.

16.

Early X chromosome inactivation during human preimplantation development revealed by single-cell RNA-sequencing.

Moreira de Mello JC, Fernandes GR, Vibranovski MD, Pereira LV.

Sci Rep. 2017 Sep 7;7(1):10794. doi: 10.1038/s41598-017-11044-z.

17.

Analysis of population-specific pharmacogenomic variants using next-generation sequencing data.

Ahn E, Park T.

Sci Rep. 2017 Sep 4;7(1):8416. doi: 10.1038/s41598-017-08468-y.

18.

Evaluating somatic tumor mutation detection without matched normal samples.

Teer JK, Zhang Y, Chen L, Welsh EA, Cress WD, Eschrich SA, Berglund AE.

Hum Genomics. 2017 Sep 4;11(1):22. doi: 10.1186/s40246-017-0118-2.

19.

Lactase persistence in Tunisia as a result of admixture with other Mediterranean populations.

Ben Halima Y, Kefi R, Sazzini M, Giuliani C, De Fanti S, Nouali C, Nagara M, Mengozzi G, Elouej S, Abid A, Jamoussi H, Chouchane L, Romeo G, Abdelhak S, Luiselli D.

Genes Nutr. 2017 Aug 24;12:20. doi: 10.1186/s12263-017-0573-3. eCollection 2017.

20.

A Comparative Analysis of Genetic Ancestry and Admixture in the Colombian Populations of Chocó and Medellín.

Conley AB, Rishishwar L, Norris ET, Valderrama-Aguirre A, Mariño-Ramírez L, Medina-Rivas MA, Jordan IK.

G3 (Bethesda). 2017 Oct 5;7(10):3435-3447. doi: 10.1534/g3.117.1118.

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