Novel GREM1 variations in Sub-Saharan African patients with cleft lip and/or cleft palate

by Abdur-Rahman, L.O, Adeyemo, A.A, Adeyemo, W.L, Agbenorku, P., Aregbesola, B.S, Audu, R., Bello, S.A, Busch, T.D, Butali, A., Donkor, P., Eshete, M.A, Gowans, L.J.J, Marazita, M.L, Mossey, P.A, Murray, J.C, Obiri-Yeboah, S., Oginni, F.O, Ogunlewe, M.O, Olaitan, P.B, Onwuamah, C., Oseni, G., Oti, A.A, Owais, A., Plange-Rhule, G.
Published 2018

A large-scale population based organelle pan-genomes construction and phylogeny analysis reveal the genetic diversity and the evolutionary origins of chloroplast and mitochondrion...

by Hua, W., Liu, H., Liu, J., Zhao, W.
Published 2022

Application of high-throughput sequencing for hereditary thrombocytopenia in southwestern China

by Dou, Y., Guan, X., Guo, Y., Luo, M., Wen, X., Xian, Y., Yu, J., Zhang, L.
Published 2021

The variations in human orphan G protein-coupled receptor QRFPR affect PI3K-AKT-mTOR signaling

by Hu, L., Li, H., Lin, X., Lou, R., Tang, S., Xiang, Y., Xu, C., Xu, X., Xu, Y., Yu, Y.
Published 2021

Intelligent Characterization of Lentil Genetic Resources: Evolutionary History, Genetic Diversity of Germplasm, and the Need for Well-Represented Collections

by Bett, K.E, Bitocchi, E., Gioia, T., Guerra-García, A., Logozzo, G., Papa, R., von Wettberg, E.
Published 2021

Significance of linkage disequilibrium and epistasis on genetic variances in noninbred and inbred populations

by Garcia, A.A.F, Viana, J.M.S
Published 2022

Exploring genetic variation and population structure in a threatened species, Noturus placidus, with whole-genome sequence data

by Decker, J.E, Durbin, H.J, Fenner, D., Johnson, G.S, Mhlanga-Mutangadura, T., Rowan, T.N, Schnabel, R.D, Tabor, V.M, Tribe, P., Whitacre, L.K, Wildhaber, M.L
Published 2022

No links between genetic variation and developing theory of mind: A preregistered replication attempt of candidate gene studies

by Kloo, D., Lesch, K.-P, Opitz, T., Osterhaus, C., Paulus, M., Schuwerk, T., Sodian, B.
Published 2021

Genetic correlates of socio-economic status influence the pattern of shared heritability across mental health traits

by Abdellaoui, A., Denys, D., Derks, E.M, Galama, T.J, Marees, A.T, Nivard, M.G, Smit, D.J.A, van den Brink, W., Verweij, K.J.H
Published 2021

Chitosan derivatives: A suggestive evaluation for novel inhibitor discovery against wild type and variants of SARS-CoV-2 virus

by Jha, A., Kumar, A., Modak, C., Sharma, N.
Published 2021

Indian genetic heritage in Southeast Asian populations

by Altınışık, N.E, Boonthai, W., Changmai, P., Flegontov, P., Flegontova, O., Inta, A., Jaisamut, K., Kampuansai, J., Kutanan, W., Pamjav, H., Reich, D., Yüncü, E.
Published 2022

The genetic architecture of pediatric cardiomyopathy

by Aronow, B., Bansal, N., Bhatnagar, S., Canter, C.E, Chung, W.K, Colan, S.D, Dexheimer, P.J, Everitt, M.D, Fan, X., Hsu, D.T, Kantor, P.F, Lal, A.K, Lee, T.M, Lipshultz, S.E, Martin, L.J, Miller, E.M, Pahl, E., Pediatric Cardiomyopathy Registry Study Group, Rossano, J.W, Rusconi, P., Schubert, J.A, Shen, Y., Shi, L., Sridhar, A., Tariq, M., Towbin, J.A, Ware, S.M, Webber, S.A, Wilkinson, J.D
Published 2022

Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates

by Harley, J.B, Hawley, M., Jarvik, G.P, Karlson, E.W, Koch, C., Lebo, M.S, Leppig, K.A, Mahanta, L.M, Myers, M.F, Oza, A., Prows, C.A, Rehm, H.L, Vijay Kumar, P.K, Weiss, S.T, Williams, M.S, Yu, W., Zouk, H.
Published 2022

VPMBench: a test bench for variant prioritization methods

by Ewald, R., Reimler, A.L, Ruscheinski, A., Uhrmacher, A.M
Published 2021

Boosting heritability: estimating the genetic component of phenotypic variation with multiple sample splitting

by Corander, J., Mai, T.T, Turner, P.
Published 2021

Evolution of phenotypic fluctuation under host-parasite interactions

by Kaneko, K., Nishiura, N.
Published 2021

Whole genome sequencing and the application of a SNP panel reveal primary evolutionary lineages and genomic variation in the lion (Panthera leo)

by Bauer, H., Bertola, L.D, Chege, M., de Iongh, H.H, Laros, J.F.J, Lesilau, F., Patterson, B.D, Schaap, O.D, Sogbohossou, E.A, Tumenta, P.N, Vermaat, M., Vrieling, K., White, P.A
Published 2022

Overcoming constraints on the detection of recessive selection in human genes from population frequency data

by Balick, D.J, Do, R., Jordan, D.M, Sunyaev, S.
Published 2022

Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

by Aguilar-Salinas, C.A, AMP-T2D-GENES, Myocardial Infarction Genetics Consortium, Antonacci-Fulton, L., Ardissino, D., Arnett, D.K, Aslibekyan, S., Atzmon, G., Ballantyne, C.M, Barajas-Olmos, F., Barzilai, N., Becker, L.C, Bielak, L.F, Bis, J.C, Blangero, J., Boehnke, M., Boerwinkle, E., Bonnycastle, L.L, Bottinger, E., Bowden, D.W, Bown, M.J, Brody, J.A, Broome, J.G, Burtt, N.P, Cade, B.E, Centeno-Cruz, F., Chaffin, M.D, Chan, E., Chang, Y.-C, Chen, Y.-D.I, Cheng, C.-Y, Choi, W.J, Chowdhury, R., Contreras-Cubas, C., Córdova, E.J, Correa, A., Cupples, L.A, Curran, J.E, Danesh, J., de Vries, P.S, DeFronzo, R.A, Doddapaneni, H., Dornbos, P., Duggirala, R., Dutcher, S.K, Ellinor, P.T, Emery, L.S, Flannick, J.A, Florez, J.C, Fornage, M., Freedman, B.I, Fuster, V., Garay-Sevilla, M.E, García-Ortiz, H., Germer, S., Gibbs, R.A, Gieger, C., Glaser, B., Gonzalez, C., Gonzalez-Villalpando, M.E, Graff, M., Graham, S.E, Grarup, N., Groop, L.C, Guo, X., Gupta, N., Han, S., Hanis, C.L, Hansen, T., He, J., Heard-Costa, N.L, Hindy, G., Hung, Y.-J, Hwang, M.Y, Irvin, M.R, Islas-Andrade, S., Jarvik, G.P, Kang, H.M, Kardia, S.L.R, Kathiresan, S., Kelly, T., Kenny, E.E, Khan, A.T, Khera, A.V, Kim, B.-J, Kim, R.W, Kim, Y.J, Koistinen, H.A, Kooperberg, C., Kuusisto, J., Kwak, S.H, Laakso, M., Lange, L.A, Lee, J., Lee, J., Lee, S., Lehman, D.M, Lemaitre, R.N, Linneberg, A., Liu, D.J, Liu, J., Loos, R.J.F, Lubitz, S.A, Lyssenko, V., Ma, R.C.W, Martin, L.W, Martínez-Hernández, A., Mathias, R.A, McCarthy, M.I, McGarvey, S.T, McPherson, R., Meigs, J.B, Meitinger, T., Melander, O., Mendoza-Caamal, E., Metcalf, G.A, Mi, X., Mohlke, K.L, Montasser, M.E, Moon, J.-Y, Moreno-Macías, H., Morrison, A.C, Muzny, D.M, Natarajan, P., Nelson, S.C, NHLBI TOPMed Lipids Working Group, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Nilsson, P.M, O'Connell, J.R, Orho-Melander, M., Orozco, L., Palmer, C.N.A, Palmer, N.D, Park, C.J, Park, J., Park, K.S, Pedersen, O., Peloso, G.M, Peralta, J.M, Peyser, P.A, Post, W.S, Preuss, M., Psaty, B.M, Qi, Q., Rader, D.J, Rao, D.C, Redline, S., Reiner, A.P, Revilla-Monsalve, C., Rich, S.S, Rotter, J.I, Samani, N., Schunkert, H., Schurmann, C., Selvaraj, M.S, Seo, D., Seo, J.-S, Sim, X., Sladek, R., Small, K.S, So, W.Y, Stilp, A.M, Tai, E.S, Tam, C.H.T, Taylor, K.D, Teo, Y.Y, Thameem, F., Tomlinson, B., Tsai, M.Y, Tuomi, T., Tuomilehto, J., Tusié-Luna, T., Udler, M.S, van Dam, R.M, Vasan, R.S, Viaud Martinez, K.A, Wang, F.F, Wang, M., Wang, X., Watkins, H., Weeks, D.E, Willer, C.J, Wilson, J.G, Witte, D.R, Wong, T.-Y, Yanek, L.R, Zhang, D.
Published 2022

Detection of CYP2C19 genetic variants in Malaysian Orang Asli from massively parallel sequencing data

by Ahmad, A., Ang, G.Y, Aziz, T.A.T.A, Isa, K.M, Ismail, A.I, James, R.J, Khalid, M.I.H.A, Nor, F.M, Rahman, T.A, Salleh, H., Salleh, M.Z, Subramaniam, V., Teh, L.K, Yu, C.Y
Published 2016