日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Clinical and analytical validation of an 82-gene comprehensive genome-profiling panel for identifying and interpreting variants responsible for inherited retinal dystrophies

对 82 个基因的综合基因组分析面板进行临床和分析验证,以识别和解释导致遗传性视网膜营养不良的变异

Jacqueline Chan, Jolyon Holdstock, John Shovelton, James Reid, Graham Speight, Duarte Molha, Venu Pullabhatla, Stephanie Carpenter, Ezam Uddin, Takanori Washio, Hiroko Sato, Yuuki Izumi, Reiko Watanabe, Hayato Niiro, Yoshiyuki Fukushima, Naoko Ashida, Takashi Hirose, Akiko Maeda

The Th1 cell regulatory circuitry is largely conserved between human and mouse

Th1细胞调控回路在人和小鼠之间基本保守。

Henderson, Stephen; Pullabhatla, Venu; Hertweck, Arnulf; de Rinaldis, Emanuele; Herrero, Javier; Lord, Graham M; Jenner, Richard G

Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02

全基因组关联研究发现额部纤维化性脱发存在四个易感基因位点,包括 HLA-B*07:02

Tziotzios, Christos; Petridis, Christos; Dand, Nick; Ainali, Chrysanthi; Saklatvala, Jake R; Pullabhatla, Venu; Onoufriadis, Alexandros; Pramanik, Rashida; Baudry, David; Lee, Sang Hyuck; Wood, Kristie; Liu, Lu; Seegobin, Seth; Michelotti, Gregory A; Lwin, Su M; Christou, Evangelos A A; Curtis, Charles J; de Rinaldis, Emanuele; Saxena, Alka; Holmes, Susan; Harries, Matthew; Palamaras, Ioulios; Cunningham, Fiona; Parkins, Gregory; Kaur, Manjit; Farrant, Paul; McDonagh, Andrew; Messenger, Andrew; Jones, Jennifer; Jolliffe, Victoria; Ali, Iaisha; Ardern-Jones, Michael; Mitchell, Charles; Burrows, Nigel; Atkar, Ravinder; Banfield, Cedric; Alexandroff, Anton; Champagne, Caroline; Cooper, Hywel L; Vañó-Galván, Sergio; Molina-Ruiz, Ana Maria; Perez, Nerea Ormaechea; Patel, Girish K; Macbeth, Abby; Page, Melanie; Bryden, Alyson; Mowbray, Megan; Wahie, Shyamal; Armstrong, Keith; Cooke, Nicola; Goodfield, Mark; Man, Irene; de Berker, David; Dunnill, Giles; Takwale, Anita; Rao, Archana; Siah, Tee-Wei; Sinclair, Rodney; Wade, Martin S; Dlova, Ncoza C; Setterfield, Jane; Lewis, Fiona; Bhargava, Kapil; Kirkpatrick, Niall; Estivill, Xavier; Stefanato, Catherine M; Flohr, Carsten; Spector, Timothy; Watt, Fiona M; Smith, Catherine H; Barker, Jonathan N; Fenton, David A; Simpson, Michael A; McGrath, John A

De novo mutations implicate novel genes in systemic lupus erythematosus

从头突变暗示系统性红斑狼疮的新基因

Venu Pullabhatla, Amy L Roberts, Myles J Lewis, Daniele Mauro, David L Morris, Christopher A Odhams, Philip Tombleson, Ulrika Liljedahl, Simon Vyse, Michael A Simpson, Sascha Sauer, Emanuele de Rinaldis, Ann-Christine Syvänen, Timothy J Vyse

An in-depth characterization of the major psoriasis susceptibility locus identifies candidate susceptibility alleles within an HLA-C enhancer element

对主要银屑病易感基因位点的深入表征,在HLA-C增强子元件中鉴定出候选易感等位基因。

Clop, Alex; Bertoni, Anna; Spain, Sarah L; Simpson, Michael A; Pullabhatla, Venu; Tonda, Raul; Hundhausen, Christian; Di Meglio, Paola; De Jong, Pieter; Hayday, Adrian C; Nestle, Frank O; Barker, Jonathan N; Bell, Robert J A; Capon, Francesca; Trembath, Richard C

Challenges associated with metal chelation therapy in Alzheimer's disease

阿尔茨海默病金属螯合疗法面临的挑战

Hegde, Muralidhar L; Bharathi, P; Suram, Anitha; Venugopal, Chitra; Jagannathan, Ramya; Poddar, Pankaj; Srinivas, Pullabhatla; Sambamurti, Kumar; Rao, Kosagisharaf Jagannatha; Scancar, Janez; Messori, Luigi; Zecca, Luigi; Zatta, Paolo