Leveraging Base Pair Mammalian Constraint to Understand Genetic Variation and Human Disease
Patrick F. Sullivan(University of North Carolina at Chapel Hill), Kerstin Lindblad‐Toh(Broad Institute), Katherine S. Pollard(QB3), Laura M. Huckins(Allen Institute for Brain Science), Andreas R. Pfenning(Howard Hughes Medical Institute), Sharadha Sakthikumar(Translational Genomics Research Institute), Matteo Bianchi(Uppsala University), Jin Szatkiewicz(Broad Institute), Michael X. Dong, Shuyang Yao(Karolinska Institutet), Jia Wen(University of North Carolina at Chapel Hill), Jian Zeng(The University of Queensland), James R. Xue(Howard Hughes Medical Institute), Steven Gazal(University of Southern California), Gregory Andrews(University of Massachusetts Chan Medical School), Voichita D. Marinescu(Science for Life Laboratory), Jennifer R. S. Meadows(University of North Carolina at Chapel Hill), Matthew J. Christmas, Diane P. Genereux(Broad Institute), Zhili Zheng(Broad Institute), Quan Sun(University of North Carolina at Chapel Hill), Jiawen Chen(University of North Carolina at Chapel Hill), Elinor K. Karlsson(Broad Institute), Karin Forsberg‐Nilsson(Uppsala University), Benedict Paten(University of California, Santa Cruz), Naomi R. Wray(The University of Queensland), Ola Wallerman(Uppsala University), Steven K. Reilly(Yale University), Alyssa J. Lawler(Broad Institute), BaDoi N. Phan(University of Pittsburgh Medical Center), Zhiping Weng(UMass Memorial Health Care), Kathleen C. Keough(Personalis (United States)), Jessica Johnson(University of North Carolina at Chapel Hill), Yun Li(Shanghai University of Traditional Chinese Medicine), Xue Li(Broad Institute), Jessika Nordin(Science for Life Laboratory), Ananya Roy(Uppsala University), Graham M. Hughes(University College Dublin)
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