70-year legacy of the Framingham Heart Study von Andersson, Charlotte, Johnson, Andrew D., Benjamin, Emelia J., Levy, Daniel, Vasan, Ramachandran S.

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GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database von Leslie, Richard, O'Donnell, Christopher J, Johnson, Andrew D

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Primordial germ cells: the first cell lineage or the last cells standing? von Johnson, Andrew D, Alberio, Ramiro

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Genome‐wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease von Yao, Chen, Chen, George, Song, Ci, Keefe, Joshua, Mendelson, Michael, Huan, Tianxiao, Sun, Benjamin B., Laser, Annika, Maranville, Joseph C., Wu, Hongsheng, Ho, Jennifer E., Courchesne, Paul, Lyass, Asya, Larson, Martin G., Gieger, Christian, Graumann, Johannes, Johnson, Andrew D., Danesh, John, Runz, Heiko, Hwang, Shih-Jen, Liu, Chunyu, Butterworth, Adam S., Suhre, Karsten, Levy, Daniel

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Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease von Huan, Tianxiao, Joehanes, Roby, Song, Ci, Peng, Fen, Guo, Yichen, Mendelson, Michael, Yao, Chen, Liu, Chunyu, Ma, Jiantao, Richard, Melissa, Agha, Golareh, Guan, Weihua, Almli, Lynn M., Conneely, Karen N., Keefe, Joshua, Hwang, Shih-Jen, Johnson, Andrew D., Fornage, Myriam, Liang, Liming, Levy, Daniel

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An open access database of genome-wide association results von Johnson, Andrew D, O'Donnell, Christopher J

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SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap von Johnson, Andrew D., Handsaker, Robert E., Pulit, Sara L., Nizzari, Marcia M., O'Donnell, Christopher J., de Bakker, Paul I. W.

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GRASP v2.0: an update on the Genome-Wide Repository of Associations between SNPs and phenotypes von Eicher, John D, Landowski, Christa, Stackhouse, Brian, Sloan, Arielle, Chen, Wenjie, Jensen, Nicole, Lien, Ju-Ping, Leslie, Richard, Johnson, Andrew D

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Identification of ciliary localization sequences within the third intracellular loop of G protein-coupled receptors von Berbari, Nicolas F, Johnson, Andrew D, Lewis, Jacqueline S, Askwith, Candice C, Mykytyn, Kirk

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Genome-wide identification of microRNA expression quantitative trait loci von Huan, Tianxiao, Rong, Jian, Liu, Chunyu, Zhang, Xiaoling, Tanriverdi, Kahraman, Joehanes, Roby, Chen, Brian H., Murabito, Joanne M., Yao, Chen, Courchesne, Paul, Munson, Peter J., O’Donnell, Christopher J., Cox, Nancy, Johnson, Andrew D., Larson, Martin G., Levy, Daniel, Freedman, Jane E.

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NANOG is required to establish the competence for germ-layer differentiation in the basal tetrapod axolotl von Simpson, Luke A, Crowley, Darren, Forey, Teri, Acosta, Helena, Ferjentsik, Zoltan, Chatfield, Jodie, Payne, Alexander, Simpson, Benjamin S, Redwood, Catherine, Dixon, James E, Holmes, Nadine, Sang, Fei, Alberio, Ramiro, Loose, Matthew, Johnson, Andrew D

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Identification of common genetic variants controlling transcript isoform variation in human whole blood von Zhang, Xiaoling, Joehanes, Roby, Chen, Brian H, Huan, Tianxiao, Ying, Saixia, Munson, Peter J, Johnson, Andrew D, Levy, Daniel, O'Donnell, Christopher J

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Cell perturbation and lasers illuminate the genetics of latent blood cell traits von Johnson, Andrew D.

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Common dysregulation network in the human prefrontal cortex underlies two neurodegenerative diseases von Narayanan, Manikandan, Huynh, Jimmy L, Wang, Kai, Yang, Xia, Yoo, Seungyeul, McElwee, Joshua, Zhang, Bin, Zhang, Chunsheng, Lamb, John R, Xie, Tao, Suver, Christine, Molony, Cliona, Melquist, Stacey, Johnson, Andrew D, Fan, Guoping, Stone, David J, Schadt, Eric E, Casaccia, Patrizia, Emilsson, Valur, Zhu, Jun

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A Platelet Function Modulator of Thrombin Activation Is Causally Linked to Cardiovascular Disease and Affects PAR4 Receptor Signaling von Rodriguez, Benjamin A.T., Bhan, Arunoday, Beswick, Andrew, Elwood, Peter C., Niiranen, Teemu J., Salomaa, Veikko, Trégouët, David-Alexandre, Morange, Pierre-Emmanuel, Civelek, Mete, Ben-Shlomo, Yoav, Schlaeger, Thorsten, Chen, Ming-Huei, Johnson, Andrew D.

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Allelic Expression Imbalance of Human mu Opioid Receptor (OPRM1) Caused by Variant A118G von Zhang, Ying, Wang, Danxin, Johnson, Andrew D., Papp, Audrey C., Sadée, Wolfgang

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Cardiovascular correlates of platelet count and volume in the Framingham Heart Study von Sloan, Arielle, BS, Gona, Philimon, PhD, Johnson, Andrew D., PhD

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A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors von Thibord, Florian, Chan, Melissa V., Chen, Ming-Huei, Johnson, Andrew D.

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Transient Accumulation of 5-Carboxylcytosine Indicates Involvement of Active Demethylation in Lineage Specification of Neural Stem Cells von Wheldon, Lee M., Abakir, Abdulkadir, Ferjentsik, Zoltan, Dudnakova, Tatiana, Strohbuecker, Stephanie, Christie, Denise, Dai, Nan, Guan, Shengxi, Foster, Jeremy M., Corrêa, Ivan R., Loose, Matthew, Dixon, James E., Sottile, Virginie, Johnson, Andrew D., Ruzov, Alexey

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Stochastic specification of primordial germ cells from mesoderm precursors in axolotl embryos von Chatfield, Jodie, O'Reilly, Marie-Anne, Bachvarova, Rosemary F, Ferjentsik, Zoltan, Redwood, Catherine, Walmsley, Maggie, Patient, Roger, Loose, Mathew, Johnson, Andrew D

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