| Genome-wide association studies E Uffelmann, QQ Huang, NS Munung, J de Vries, Y Okada, AR Martin, ... Nature Reviews Methods Primers 1 (1), 1-21, 2021 | 1023 | 2021 |
| Mapping the human genetic architecture of COVID-19 Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ... Nature 600 (7889), 472-477, 2021 | 740 | 2021 |
| The power of genetic diversity in genome-wide association studies of lipids SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ... Nature 600 (7890), 675-679, 2021 | 432 | 2021 |
| Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations MH Chen, LM Raffield, A Mousas, S Sakaue, JE Huffman, A Moscati, ... Cell 182 (5), 1198-1213. e14, 2020 | 424 | 2020 |
| MicroRNAs and their isomiRs function cooperatively to target common biological pathways N Cloonan, S Wani, Q Xu, J Gu, K Lea, S Heater, C Barbacioru, ... Genome biology 12, 1-20, 2011 | 412 | 2011 |
| Factors influencing success of clinical genome sequencing across a broad spectrum of disorders JC Taylor, HC Martin, S Lise, J Broxholme, JB Cazier, A Rimmer, ... Nature genetics 47 (7), 717-726, 2015 | 409 | 2015 |
| Evidence for 28 genetic disorders discovered by combining healthcare and research data J Kaplanis, KE Samocha, L Wiel, Z Zhang, KJ Arvai, RY Eberhardt, ... Nature 586 (7831), 757-762, 2020 | 398 | 2020 |
| Common genetic variants contribute to risk of rare severe neurodevelopmental disorders MEK Niemi, HC Martin, DL Rice, G Gallone, S Gordon, M Kelemen, ... Nature 562 (7726), 268, 2018 | 301 | 2018 |
| Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis HC Martin, GE Kim, AT Pagnamenta, Y Murakami, GL Carvill, E Meyer, ... Human molecular genetics 23 (12), 3200-3211, 2014 | 279 | 2014 |
| Whole-genome sequencing reveals host factors underlying critical COVID-19 A Kousathanas, E Pairo-Castineira, K Rawlik, A Stuckey, CA Odhams, ... Nature 607 (7917), 97-103, 2022 | 235 | 2022 |
| Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant J Li, SL Woods, S Healey, J Beesley, X Chen, JS Lee, H Sivakumaran, ... The American Journal of Human Genetics 98 (5), 830-842, 2016 | 224 | 2016 |
| Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease W Zhou, M Kanai, KHH Wu, H Rasheed, K Tsuo, JB Hirbo, Y Wang, ... Cell Genomics 2 (10), 2022 | 200 | 2022 |
| Geographical genomics of human leukocyte gene expression variation in southern Morocco Y Idaghdour, W Czika, KV Shianna, SH Lee, PM Visscher, HC Martin, ... Nature genetics 42 (1), 62-67, 2010 | 186 | 2010 |
| Quantifying the contribution of recessive coding variation to developmental disorders HC Martin, WD Jones, R McIntyre, G Sanchez-Andrade, M Sanderson, ... Science 362 (6419), 1161-1164, 2018 | 172 | 2018 |
| Whole-genome sequencing of bladder cancers reveals somatic CDKN1A mutations and clinicopathological associations with mutation burden JB Cazier, SR Rao, CM McLean, AK Walker, BJ Wright, EEM Jaeger, ... Nature communications 5, 3756, 2014 | 169 | 2014 |
| miR-139-5p is a regulator of metastatic pathways in breast cancer K Krishnan, AL Steptoe, HC Martin, DR Pattabiraman, K Nones, ... Rna 19 (12), 1767-1780, 2013 | 167 | 2013 |
| MicroRNA-182-5p targets a network of genes involved in DNA repair K Krishnan, AL Steptoe, HC Martin, S Wani, K Nones, N Waddell, ... RNA 19 (2), 230-242, 2013 | 157 | 2013 |
| Imperfect centered miRNA binding sites are common and can mediate repression of target mRNAs HC Martin, S Wani, AL Steptoe, K Krishnan, K Nones, E Nourbakhsh, ... Genome biology 15 (3), R51, 2014 | 156 | 2014 |
| Evaluating drug targets through human loss-of-function genetic variation EV Minikel, KJ Karczewski, HC Martin, BB Cummings, N Whiffin, ... Nature 581 (7809), 459-464, 2020 | 139 | 2020 |
| Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility H Mbarek, S Steinberg, DR Nyholt, SD Gordon, MB Miller, AF McRae, ... The American Journal of Human Genetics 98 (5), 898-908, 2016 | 131 | 2016 |
Qin Qin HuangStaff Scientist, Wellcome Sanger Institute在 sanger.ac.uk 的电子邮件经过验证
