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

Rare variants analyses suggest novel cleft genes in the African population

罕见变异分析表明,非洲人群中存在新的唇腭裂基因

Alade, Azeez; Mossey, Peter; Awotoye, Waheed; Busch, Tamara; Oladayo, Abimbola M; Aladenika, Emmanuel; Olujitan, Mojisola; Wentworth, Emma; Anand, Deepti; Naicker, Thirona; Gowans, Lord J J; Eshete, Mekonen A; Adeyemo, Wasiu L; Zeng, Erliang; Van Otterloo, Eric; O'Rorke, Michael; Adeyemo, Adebowale; Murray, Jeffrey C; Cotney, Justin; Lachke, Salil A; Romitti, Paul; Butali, Azeez

High-Throughput Transcriptomics of Celf1 Conditional Knockout Lens Identifies Downstream Networks Linked to Cataract Pathology

Celf1条件性敲除晶状体的高通量转录组学分析揭示了与白内障病理相关的下游网络

Siddam, Archana D; Duot, Matthieu; Coomson, Sarah Y; Anand, Deepti; Aryal, Sandeep; Weatherbee, Bailey A T; Audic, Yann; Paillard, Luc; Lachke, Salil A

Proteomic profiling of retina and retinal pigment epithelium combined embryonic tissue to facilitate ocular disease gene discovery

对视网膜和视网膜色素上皮联合胚胎组织进行蛋白质组学分析,以促进眼部疾病基因的发现。

Aryal, Sandeep; Anand, Deepti; Huang, Hongzhan; Reddy, Ashok P; Wilmarth, Phillip A; David, Larry L; Lachke, Salil A

Misconduct in Biomedical Research: A Meta-Analysis and Systematic Review

生物医学研究中的不端行为:一项荟萃分析和系统评价

Phogat, Ritu; Manjunath, Bhadravathi Cheluvaiah; Sabbarwal, Bhavna; Bhatnagar, Anurag; Reena; Anand, Deepti

Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate

全基因组测序揭示与非综合征型唇腭裂相关的新生突变

Awotoye, Waheed; Mossey, Peter A; Hetmanski, Jacqueline B; Gowans, Lord J J; Eshete, Mekonen A; Adeyemo, Wasiu L; Alade, Azeez; Zeng, Erliang; Adamson, Olawale; Naicker, Thirona; Anand, Deepti; Adeleke, Chinyere; Busch, Tamara; Li, Mary; Petrin, Aline; Aregbesola, Babatunde S; Braimah, Ramat O; Oginni, Fadekemi O; Oladele, Ayodeji O; Oladayo, Abimbola; Kayali, Sami; Olotu, Joy; Hassan, Mohaned; Pape, John; Donkor, Peter; Arthur, Fareed K N; Obiri-Yeboah, Solomon; Sabbah, Daniel K; Agbenorku, Pius; Plange-Rhule, Gyikua; Oti, Alexander Acheampong; Gogal, Rose A; Beaty, Terri H; Taub, Margaret; Marazita, Mary L; Schnieders, Michael J; Lachke, Salil A; Adeyemo, Adebowale A; Murray, Jeffrey C; Butali, Azeez

Genomic analyses in African populations identify novel risk loci for cleft palate

非洲人群的基因组分析发现了新的腭裂风险基因位点

Butali, Azeez; Mossey, Peter A; Adeyemo, Wasiu L; Eshete, Mekonen A; Gowans, Lord J J; Busch, Tamara D; Jain, Deepti; Yu, Wenjie; Huan, Liu; Laurie, Cecelia A; Laurie, Cathy C; Nelson, Sarah; Li, Mary; Sanchez-Lara, Pedro A; Magee, William P; Magee, Kathleen S; Auslander, Allyn; Brindopke, Frederick; Kay, Denise M; Caggana, Michele; Romitti, Paul A; Mills, James L; Audu, Rosemary; Onwuamah, Chika; Oseni, Ganiyu O; Owais, Arwa; James, Olutayo; Olaitan, Peter B; Aregbesola, Babatunde S; Braimah, Ramat O; Oginni, Fadekemi O; Oladele, Ayodeji O; Bello, Saidu A; Rhodes, Jennifer; Shiang, Rita; Donkor, Peter; Obiri-Yeboah, Solomon; Arthur, Fareed Kow Nanse; Twumasi, Peter; Agbenorku, Pius; Plange-Rhule, Gyikua; Oti, Alexander Acheampong; Ogunlewe, Olugbenga M; Oladega, Afisu A; Adekunle, Adegbayi A; Erinoso, Akinwunmi O; Adamson, Olatunbosun O; Elufowoju, Abosede A; Ayelomi, Oluwanifemi I; Hailu, Taiye; Hailu, Abiye; Demissie, Yohannes; Derebew, Miliard; Eliason, Steve; Romero-Bustillous, Miguel; Lo, Cynthia; Park, James; Desai, Shaan; Mohammed, Muiawa; Abate, Firke; Abdur-Rahman, Lukman O; Anand, Deepti; Saadi, Irfaan; Oladugba, Abimibola V; Lachke, Salil A; Amendt, Brad A; Rotimi, Charles N; Marazita, Mary L; Cornell, Robert A; Murray, Jeffrey C; Adeyemo, Adebowale A

Molecular characterization of the human lens epithelium-derived cell line SRA01/04.

人晶状体上皮衍生细胞系 SRA01/04 的分子特征

Weatherbee Bailey A T, Barton Joshua R, Siddam Archana D, Anand Deepti, Lachke Salil A

iSyTE 2.0: a database for expression-based gene discovery in the eye

iSyTE 2.0:一个基于表达谱的眼科基因发现数据库

Kakrana, Atul; Yang, Andrian; Anand, Deepti; Djordjevic, Djordje; Ramachandruni, Deepti; Singh, Abhyudai; Huang, Hongzhan; Ho, Joshua W K; Lachke, Salil A

Mutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects

转录因子基因FOXE3、HSF4、MAF和PITX3的突变更新,导致白内障和其他发育性眼部缺陷。

Anand, Deepti; Agrawal, Smriti A; Slavotinek, Anne; Lachke, Salil A

RNA sequencing-based transcriptomic profiles of embryonic lens development for cataract gene discovery

基于RNA测序的胚胎晶状体发育转录组分析用于白内障基因发现

Anand, Deepti; Kakrana, Atul; Siddam, Archana D; Huang, Hongzhan; Saadi, Irfan; Lachke, Salil A