Publications:

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Detecting selection in low-coverage high-throughput sequencing data using principal component analysis.

Bmc Bioinformatics

Meisner, Jonas J; Albrechtsen, Anders A; Hanghøj, Kristian K

Publication Date: 2021-09-29

Variant appearance in text: rs6754311

PubMed Link: 34587903

Variant Present in the following documents:

• Main text

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Assessment of the effectiveness of the EUROFORGEN NAME and Precision ID Ancestry panel markers for ancestry investigations.

Scientific Reports

Truelsen, D D; Tvedebrink, T T; Mogensen, H S HS; Farzad, M S MS; Shan, M A MA; Morling, N N; Pereira, V V; Børsting, C C

Publication Date: 2021-09-20

Variant appearance in text: rs6754311

PubMed Link: 34545122

Variant Present in the following documents:

• Main text
• 41598_2021_Article_97654.pdf

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Evidence for a causal association between milk intake and cardiometabolic disease outcomes using a two-sample Mendelian Randomization analysis in up to 1,904,220 individuals.

International Journal Of Obesity (2005)

Vimaleswaran, Karani Santhanakrishnan KS; Zhou, Ang A; Cavadino, Alana A; Hyppönen, Elina E

Publication Date: 2021-08

Variant appearance in text: rs6754311

PubMed Link: 34024907

Variant Present in the following documents:

• Main text
• 41366_2021_Article_841.pdf

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DCDC2 READ1 regulatory element: how temporal processing differences may shape language.

Proceedings. Biological Sciences

Tang, Kevin K; DeMille, Mellissa M C MMC; Frijters, Jan C JC; Gruen, Jeffrey R JR

Publication Date: 2020-06-10

Variant appearance in text: rs6754311

PubMed Link: 32486976

Variant Present in the following documents:

• rspb20192712supp1.pdf

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GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci.

Human Molecular Genetics

Jones, Amy V AV; Tilley, Mera M; Gutteridge, Alex A; Hyde, Craig C; Nagle, Michael M; Ziemek, Daniel D; Gorman, Donal D; Fauman, Eric B EB; Chen, Xing X; Miller, Melissa R MR; Tian, Chao C; Hu, Youna Y; Hinds, David A DA; Cox, Peter P; Scollen, Serena S

Publication Date: 2017-04-01

Variant appearance in text: rs6754311

PubMed Link: 28199695

Variant Present in the following documents:

• Main text
• ddx036.pdf

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Was ADH1B under Selection in European Populations?

American Journal Of Human Genetics

Shen, Quan-Kuan QK; Sulaiman, Xierzhatijiang X; Yao, Yong-Gang YG; Peng, Min-Sheng MS; Zhang, Ya-Ping YP

Publication Date: 2016-11-03

Variant appearance in text: rs6754311

PubMed Link: 27814524

Variant Present in the following documents:

• Main text

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Ancestry-based stratified analysis of Immunochip data identifies novel associations with celiac disease.

European Journal Of Human Genetics : Ejhg

Garcia-Etxebarria, Koldo K; Jauregi-Miguel, Amaia A; Romero-Garmendia, Irati I; Plaza-Izurieta, Leticia L; Legarda, Maria M; Irastorza, Iñaki I; Bilbao, Jose Ramon JR

Publication Date: 2016-12

Variant appearance in text: rs6754311

PubMed Link: 27650971

Variant Present in the following documents:

• Main text

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Human adaptation and population differentiation in the light of ancient genomes.

Nature Communications

Key, Felix M FM; Fu, Qiaomei Q; Romagné, Frédéric F; Lachmann, Michael M; Andrés, Aida M AM

Publication Date: 2016-03-18

Variant appearance in text: rs6754311

PubMed Link: 26988143

Variant Present in the following documents:

• ncomms10775.pdf

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Fast Principal-Component Analysis Reveals Convergent Evolution of ADH1B in Europe and East Asia.

American Journal Of Human Genetics

Galinsky, Kevin J KJ; Bhatia, Gaurav G; Loh, Po-Ru PR; Georgiev, Stoyan S; Mukherjee, Sayan S; Patterson, Nick J NJ; Price, Alkes L AL

Publication Date: 2016-03-03

Variant appearance in text: rs6754311

PubMed Link: 26924531

Variant Present in the following documents:

• Main text

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Fine-scale human genetic structure in Western France.

European Journal Of Human Genetics : Ejhg

Karakachoff, Matilde M; Duforet-Frebourg, Nicolas N; Simonet, Floriane F; Le Scouarnec, Solena S; Pellen, Nadine N; Lecointe, Simon S; Charpentier, Eric E; Gros, Françoise F; Cauchi, Stéphane S; Froguel, Philippe P; Copin, Nane N; , ; Le Tourneau, Thierry T; Probst, Vincent V; Le Marec, Hervé H; Molinaro, Sabrina S; Balkau, Beverley B; Redon, Richard R; Schott, Jean-Jacques JJ; Blum, Michael Gb MG; Dina, Christian C; ,

Publication Date: 2015-06

Variant appearance in text: rs6754311

PubMed Link: 25182131

Variant Present in the following documents:

• Main text

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Seven newly identified loci for autoimmune thyroid disease.

Human Molecular Genetics

Cooper, Jason D JD; Simmonds, Matthew J MJ; Walker, Neil M NM; Burren, Oliver O; Brand, Oliver J OJ; Guo, Hui H; Wallace, Chris C; Stevens, Helen H; Coleman, Gillian G; , ; Franklyn, Jayne A JA; Todd, John A JA; Gough, Stephen C L SC

Publication Date: 2012-12-01

Variant appearance in text: rs6754311

PubMed Link: 22922229

Variant Present in the following documents:

• supp_dds357_dds357supp.pdf

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Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection.

American Journal Of Human Genetics

Bhatia, Gaurav G; Patterson, Nick N; Pasaniuc, Bogdan B; Zaitlen, Noah N; Genovese, Giulio G; Pollack, Samuela S; Mallick, Swapan S; Myers, Simon S; Tandon, Arti A; Spencer, Chris C; Palmer, Cameron D CD; Adeyemo, Adebowale A AA; Akylbekova, Ermeg L EL; Cupples, L Adrienne LA; Divers, Jasmin J; Fornage, Myriam M; Kao, W H Linda WH; Lange, Leslie L; Li, Mingyao M; Musani, Solomon S; Mychaleckyj, Josyf C JC; Ogunniyi, Adesola A; Papanicolaou, George G; Rotimi, Charles N CN; Rotter, Jerome I JI; Ruczinski, Ingo I; Salako, Babatunde B; Siscovick, David S DS; Tayo, Bamidele O BO; Yang, Qiong Q; McCarroll, Steve S; Sabeti, Pardis P; Lettre, Guillaume G; De Jager, Phil P; Hirschhorn, Joel J; Zhu, Xiaofeng X; Cooper, Richard R; Reich, David D; Wilson, James G JG; Price, Alkes L AL

Publication Date: 2011-09-09

Variant appearance in text: rs6754311

PubMed Link: 21907010

Variant Present in the following documents:

• Main text

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