| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
| 2022 | Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data | Wainschtein, P; Jain, D; Zheng, Z; Cupples, LA; Shadyab, AH; McKnight, B; Shoemaker, BM; Mitchell, BD; Psaty, BM; Kooperberg, C; Liu, CT; Albert, CM; Roden, D; Chasman, DI; Darbar, D; Lloyd-Jones, DM; Arnett, DK; Regan, EA; Boerwinkle, E; Rotter, JI; O'Connell, JR; Yanek, LR; de Andrade, M; Allison, MA; McDonald, MN; Chung, MK; Fornage, M; Chami, N; Smith, NL; Ellinor, PT; Vasan, RS; Mathias, RA; Loos, RJF; Rich, SS; Lubitz, SA; Heckbert, SR; Redline, S; Guo, X; Chen, Y-I; Laurie, CA; Hernandez, RD; McGarvey, ST; Goddard, ME; Laurie, CC; North, KE; Lange, LA; Weir, BS; Yengo, L; Yang, J; Visscher, PM; TOPMed Anthropometry Working Group; Chang, YC ; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium | Nature genetics 54(3), 263-273 | | | |
| 2021 | Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices | Natarajan, P; Pampana, A; Graham, SE; Ruotsalainen, SE; Perry, JA; de Vries, PS; Broome, JG; Pirruccello, JP; Honigberg, MC; Aragam, K; Wolford, B; Brody, JA; Antonacci-Fulton, L; Arden, M; Aslibekyan, S; Assimes, TL; Ballantyne, CM; Bielak, LF; Bis, JC; Cade, BE; Do, R; Doddapaneni, H; Emery, LS; Hung, YJ; Irvin, MR; Khan, AT; Lange, L; Lee, J; Lemaitre, RN; Martin, LW; Metcalf, G; Montasser, ME; Moon, JY; Muzny, D; O'Connell, JR; Palmer, ND; Peralta, JM; Peyser, PA; Stilp, AM; Tsai, M; Wang, FF; Weeks, DE; Yanek, LR; Wilson, JG; Abecasis, G; Arnett, DK; Becker, LC; Blangero, J; Boerwinkle, E; Bowden, DW; Chang, YC ; Chen, YI; Choi, WJ; Correa, A; Curran, JE; Daly, MJ; Dutcher, SK; Ellinor, PT; Fornage, M; Freedman, BI; Gabriel, S; Germer, S; Gibbs, RA; He, J; Hveem, K; Jarvik, GP; Kaplan, RC; Kardia, SLR; Kenny, E; Kim, RW; Kooperberg, C; Laurie, CC; Lee, S; Lloyd-Jones, DM; Loos, RJF; Lubitz, SA; Mathias, RA; Martinez, KAV; McGarvey, ST; Mitchell, BD; Nickerson, DA; North, KE; Palotie, A; Park, CJ; Psaty, BM; Rao, DC; Redline, S; Reiner, AP; Seo, D; Seo, JS; Smith, AV; Tracy, RP; Vasan, RS; Kathiresan, S; Cupples, LA; Rotter, JI; Morrison, AC; Rich, SS; Ripatti, S; Willer, C; Peloso, GM | Nature communications 12, 2182 | | | |
| 2022 | Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes | Hindy, G; Dornbos, P; Chaffin, MD; Liu, DJ; Wang, M; Selvaraj, MS; Zhang, D; Park, J; Aguilar-Salinas, CA; Antonacci-Fulton, L; Ardissino, D; Arnett, DK; Aslibekyan, S; Atzmon, G; Ballantyne, CM; Barajas-Olmos, F; Barzilai, N; Becker, LC; Bielak, LF; Bis, JC; Blangero, J; Boerwinkle, E; Bonnycastle, LL; Bottinger, E; Bowden, DW; Bown, MJ; Brody, JA; Broome, JG; Burtt, NP; Cade, BE; Centeno-Cruz, F; Chan, E; Chang, YC ; Chen, YI; Cheng, CY; Choi, WJ; Chowdhury, R; Contreras-Cubas, C; Cordova, EJ; Correa, A; Cupples, LA; Curran, JE; Danesh, J; de Vries, PS; DeFronzo, RA; Doddapaneni, H; Duggirala, R; Dutcher, SK; Ellinor, PT; Emery, LS; Florez, JC; Fornage, M; Freedman, BI; Fuster, V; Garay-Sevilla, ME; Garcia-Ortiz, H; Germer, S; Gibbs, RA; Gieger, C; Glaser, B; Gonzalez, C; Gonzalez-Villalpando, ME; Graff, M; Graham, SE; Grarup, N; Groop, LC; Guo, X; Gupta, N; Han, S; Hanis, CL; Hansen, T; He, J; Heard-Costa, NL; Hung, YJ; Hwang, MY; Irvin, MR; Islas-Andrade, S; Jarvik, GP; Kang, HM; Kardia, SLR; Kelly, T; Kenny, EE; Khan, AT; Kim, BJ; Kim, RW; Kim, YJ; Koistinen, HA; Kooperberg, C; Kuusisto, J; Kwak, SH; Laakso, M; Lange, LA; Lee, J; Lee, J; Lee, S; Lehman, DM; Lemaitre, RN; Linneberg, A; Liu, J; Loos, RJF; Lubitz, SA; Lyssenko, V; Ma, RCW; Martin, LW; Martinez-Hernandez, A; Mathias, RA; McGarvey, ST; McPherson, R; Meigs, JB; Meitinger, T; Melander, O; Mendoza-Caamal, E; Metcalf, GA; Mi, X; Mohlke, KL; Montasser, ME; Moon, JY; Moreno-Macias, H; Morrison, AC; Muzny, DM; Nelson, SC; Nilsson, PM; O'Connell, JR; Orho-Melander, M; Orozco, L; Palmer, CNA; Palmer, ND; Park, CJ; Park, KS; Pedersen, O; Peralta, JM; Peyser, PA; Post, WS; Preuss, M; Psaty, BM; Qi, Q; Rao, DC; Redline, S; Reiner, AP; Revilla-Monsalve, C; Rich, SS; Samani, N; Schunkert, H; Schurmann, C; Seo, D; Seo, JS; Sim, X; Sladek, R; Small, KS; So, WY; Stilp, AM; Tai, ES; Tam, CHT; Taylor, KD; Teo, YY; Thameem, F; Tomlinson, B; Tsai, MY; Tuomi, T; Tuomilehto, J; Tusie-Luna, T; Udler, MS; van Dam, RM; Vasan, RS; Viaud Martinez, KA; Wang, FF; Wang, X; Watkins, H; Weeks, DE; Wilson, JG; Witte, DR; Wong, TY; Yanek, LR; Kathiresan, S; Rader, DJ; Rotter, JI; Boehnke, M; McCarthy, MI; Willer, CJ; Natarajan, P; Flannick, JA; Khera, AV; Peloso, GM | American journal of human genetics 109(1), 81-96 | | | |
| 2022 | Rare coding variants in RCN3 are associated with blood pressure | He, KY; Kelly, TN; Wang, H; Liang, J; Zhu, L; Cade, BE; Assimes, TL; Becker, LC; Beitelshees, AL; Bielak, LF; Bress, AP; Brody, JA; Chang, YC; Chang, YC ; de Vries, PS; Duggirala, R; Fox, ER; Franceschini, N; Furniss, AL; Gao, Y; Guo, X; Haessler, J; Hung, YJ; Hwang, SJ; Irvin, MR; Kalyani, RR; Liu, CT; Liu, C; Martin, LW; Montasser, ME; Muntner, PM; Mwasongwe, S; Naseri, T; Palmas, W; Reupena, MS; Rice, KM; Sheu, WH; Shimbo, D; Smith, JA; Snively, BM; Yanek, LR; Zhao, W; Blangero, J; Boerwinkle, E; Chen, YI; Correa, A; Cupples, LA; Curran, JE; Fornage, M; He, J; Hou, L; Kaplan, RC; Kardia, SLR; Kenny, EE; Kooperberg, C; Lloyd-Jones, D; Loos, RJF; Mathias, RA; McGarvey, ST; Mitchell, BD; North, KE; Peyser, PA; Psaty, BM; Raffield, LM; Rao, DC; Redline, S; Reiner, AP; Rich, SS; Rotter, JI; Taylor, KD; Tracy, R; Vasan, RS; Morrison, AC; Levy, D; Chakravarti, A; Arnett, DK; Zhu, X | BMC genomics 23(1), 148 | | | |
