| Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ... Cell 179 (7), 1469-1482. e11, 2019 | 1416 | 2019 |
| Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa HJ Watson, Z Yilmaz, LM Thornton, C Hübel, JRI Coleman, HA Gaspar, ... Nature genetics 51 (8), 1207-1214, 2019 | 1278 | 2019 |
| The diploid genome sequence of an Asian individual J Wang, W Wang, R Li, Y Li, G Tian, L Goodman, W Fan, J Zhang, J Li, ... Nature 456 (7218), 60-65, 2008 | 1190 | 2008 |
| Draft genome of the wheat A-genome progenitor Triticum urartu HQ Ling, S Zhao, D Liu, J Wang, H Sun, C Zhang, H Fan, D Li, L Dong, ... Nature 496 (7443), 87-90, 2013 | 902 | 2013 |
| Complete resequencing of 40 genomes reveals domestication events and genes in silkworm (Bombyx) Q Xia, Y Guo, Z Zhang, D Li, Z Xuan, Z Li, F Dai, Y Li, D Cheng, R Li, ... Science 326 (5951), 433-436, 2009 | 501 | 2009 |
| Whole-genome sequencing of giant pandas provides insights into demographic history and local adaptation S Zhao, P Zheng, S Dong, X Zhan, Q Wu, X Guo, Y Hu, W He, S Zhang, ... Nature Genetics 45 (1), 67-71, 2013 | 394 | 2013 |
| A genome-wide association study of anorexia nervosa V Boraska, CS Franklin, JAB Floyd, LM Thornton, LM Huckins, L Southam, ... Molecular psychiatry 19 (10), 1085-1094, 2014 | 392 | 2014 |
| Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases YR Li, J Li, SD Zhao, JP Bradfield, FD Mentch, SM Maggadottir, C Hou, ... Nature medicine 21 (9), 1018-1027, 2015 | 315 | 2015 |
| Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders and known risk factors N Mullins, J Kang, AI Campos, JRI Coleman, AC Edwards, H Galfalvy, ... Biological Psychiatry, 2021 | 266 | 2021 |
| Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis JA Martignetti, L Tian, D Li, MCM Ramirez, O Camacho-Vanegas, ... The American Journal of Human Genetics 92 (6), 1001-1007, 2013 | 223 | 2013 |
| ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor D Li, ME March, A Gutierrez-Uzquiza, C Kao, C Seiler, E Pinto, ... Nature medicine, 1, 2019 | 221 | 2019 |
| GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers D Li, H Yuan, XR Ortiz-Gonzalez, ED Marsh, L Tian, EM McCormick, ... The American Journal of Human Genetics 99 (4), 802-816, 2016 | 188 | 2016 |
| CYP3A4 mutation causes vitamin D-dependent rickets type 3 JD Roizen, D Li, L O'Lear, MK Javaid, NJ Shaw, PR Ebeling, HH Nguyen, ... The Journal of clinical investigation 128 (5), 1913, 2018 | 131 | 2018 |
| KAT6A Syndrome: Genotype–phenotype correlation in 76 patients with pathogenic KAT6A variants J Kennedy, D Goudie, E Blair, K Chandler, S Joss, V McKay, A Green, ... Genetics in medicine 21 (4), 850-860, 2019 | 124 | 2019 |
| Gene domain-specific DNA methylation episignatures highlight distinct molecular entities of ADNP syndrome EG Bend, E Aref-Eshghi, DB Everman, RC Rogers, SS Cathey, EJ Prijoles, ... Clinical epigenetics 11 (1), 64, 2019 | 115 | 2019 |
| CYP3A4 Induction by Rifampin: An Alternative Pathway for Vitamin D Inactivation in Patients With CYP24A1 Mutations CP Hawkes, D Li, H Hakonarson, KE Meyers, KE Thummel, MA Levine The Journal of Clinical Endocrinology & Metabolism 102 (5), 1440-1446, 2017 | 111 | 2017 |
| Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly D Li, TL Wenger, C Seiler, ME March, A Gutierrez-Uzquiza, C Kao, E Bhoj, ... Human molecular genetics, 2018 | 106 | 2018 |
| Autosomal dominant hypoparathyroidism caused by germline mutation in GNA11: phenotypic and molecular characterization D Li, EE Opas, F Tuluc, DL Metzger, C Hou, H Hakonarson, MA Levine The Journal of Clinical Endocrinology & Metabolism 99 (9), E1774-E1783, 2014 | 104 | 2014 |
| Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index A Hinney, M Kesselmeier, S Jall, AL Volckmar, M Föcker, J Antel, ... Molecular psychiatry 22 (2), 192, 2017 | 99 | 2017 |
| Mitochondrial Disease Sequence Data Resource (MSeqDR): A global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data … MJ Falk, L Shen, M Gonzalez, J Leipzig, MT Lott, APM Stassen, ... Molecular genetics and metabolism 114 (3), 388-396, 2015 | 97 | 2015 |
