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R

Reiner A. Veitia

université paris cité and cnrs and institut jacques monod

65H指数
283论文数
1.3W被引数
收录论文 143
发表时间
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Nonlinearities and Switch-Like Behavior in Gene Expression: From Genetics to Biochemistry and Back基因表达中的非线性与开关样行为：从遗传学到生物化学的往返研究
errFASEB Journal
IF4.2
err2026-09-01
err0
errOAAI
errReiner A. Veitia; James A. Birchler
err分享
err收藏
Modification of the Transcription Factor FOXL2 at Serines 101 and 107 Disables DNA Binding, Leads to Nucleolar Relocalization, and Rewires Granulosa-Cell Programs丝氨酸101和107位转录因子FOXL2的修饰会破坏DNA结合，导致核仁重定位，并重塑颗粒细胞程序
errFASEB Journal
IF4.2
err2026-08-19
err0
errOAAI
errLudovic Mousseron; Despoina Chousianiti; Francis Poulat; Bérangère Legois; Reiner A. Veitia; Anne-Laure Todeschini
err分享
err收藏
Deciphering the impact of AKT1 pathogenic variants in Juvenile Granulosa Cell Tumors Using a Drosophila model.使用果蝇模型解析AKT1致病性变异在幼年颗粒细胞瘤中的影响。
errMolecular & Cellular Proteomics
IF5.5
err2025-11-13
err0
errOAAI
errReiner A. Veitia; Laetitia Herman; Bérangère Legois; Sandra Claret; Alain Zider; Anne-Laure Todeschini
err分享
err收藏
Gene Dosage Sensitivity and Human Genetic Diseases基因剂量敏感性与人类遗传病
errJournal of Inherited Metabolic Disease
IF3.8
err2025-07-09
err0
errOAAI
errReiner A. Veitia; Johannes Zschocke; James A. Birchler
err分享
err收藏
Reclassifying NOBOX variants in primary ovarian insufficiency cases with a corrected gene model and a novel quantitative framework使用校正后的基因模型和一种新型定量框架，对原发性卵巢功能不全病例中的NOBOX变异进行重新分类
errHUMAN REPRODUCTION
IF6.1
err2025-04-17
err0
PREAI
errVeitia, Reiner A.; Cowles, Jamie D.; Caburet, Sandrine
err分享
err收藏
Emerging links between phase separation and transcription factor haploinsufficiency
errTRENDS IN GENETICS
IF16.3
err2024-12-01
err0
PREAI
errVeitia, Reiner A.
err分享
err收藏
A cellular model provides insights into the pathogenicity of the oncogenic FOXL2 somatic variant p.Cys134Trp
errBRITISH JOURNAL OF CANCER
IF6.8
err2024-03-01
err2
PREAI
errHerman, Laetitia; Amo, Angelique; Legois, Berangere; Di Carlo, Caterina; Veitia, Reiner A.; Todeschini, Anne-Laure
err分享
err收藏
The forkhead DNA-binding domain binds specific G2-rich RNA sequences
errNUCLEIC ACIDS RESEARCH
IF13.1
err2023-11-02
err2
errOAAI
errZutterling, Caroline; Todeschini, Anne-Laure; Fourmy, Deborah; Busso, Didier; Veaute, Xavier; Duconge, Frederic; Veitia, Reiner A.
err分享
err收藏
Dominant negative variants and cotranslational assembly of macromolecular complexes大分子复合物的显性负变体和共翻译组装
errBIOESSAYS
IF2.7
err2023-08-08
err1
errOAAI
errVeitia, Reiner A.
err分享
err收藏
The Oncogenic FOXL2 C134W Mutation Is a Key Driver of Granulosa Cell Tumors
errCANCER RESEARCH
IF16.6
err2022-11-21
err9
errOAAI
errLlano, Elena; Laure Todeschini, Anne; Felipe-Medina, Natalia; Corte-Torres, Maria D.; Condezo, Yazmine B.; Sanchez-Martin, Manuel; Lopez-Tamargo, Sara; Astudillo, Aurora; Puente, Xose S.; Pendas, Alberto M.; Veitia, Reiner A.
err分享
err收藏
Who ever thought genetic mutations were random
errTRENDS IN PLANT SCIENCE
IF20.8
err2022-08-01
err0
PREAI
errVeitia, Reiner A.
err分享
err收藏
A truncating variant of RAD51B associated with primary ovarian insufficiency provides insights into its meiotic and somatic functions
errCELL DEATH AND DIFFERENTIATION
IF15.4
err2022-05-27
err4
errOAAI
errFranca, Monica M.; Condezo, Yazmine B.; Elzaiat, Maeva; Felipe-Medina, Natalia; Sanchez-Saez, Fernando; Munoz, Sergio; Sainz-Urruela, Raquel; Rosario Martin-Hervas, M.; Garcia-Valiente, Rodrigo; Sanchez-Martin, Manuel A.; Astudillo, Aurora; Mendez, Juan; Llano, Elena; Veitia, Reiner A.; Mendonca, Berenice B.; Pendas, Alberto M.
err分享
err收藏
Gene-dosage issues: a recurrent theme in whole genome duplication events
errTRENDS IN GENETICS
IF16.3
err2022-01-01
err11
errOAAI
errVeitia, Reiner A.; Birchler, James A.
err分享
err收藏
FOXL2 in adult-type granulosa cell tumour of the ovary: oncogene or tumour suppressor gene?
errJOURNAL OF PATHOLOGY
IF5.2
err2021-09-01
err13
PREAI
errPilsworth, Jessica A.; Todeschini, Anne-Laure; Neilson, Samantha J.; Cochrane, Dawn R.; Lai, Daniel; Anttonen, Mikko; Heikinheimo, Markku; Huntsman, David G.; Veitia, Reiner A.
err分享
err收藏
Reply to An alternative miRISC targets a cancer-associated coding sequence mutation in FOXL2
errEMBO JOURNAL
IF8.3
err2021-08-16
err2
errOAAI
errVeitia, Reiner A.; Pilsworth, Jessica; Todeschini, Anne-Laure; Huntsman, David
err分享
err收藏
Forkhead Transcription Factors in Health and Disease
errTRENDS IN GENETICS
IF16.3
err2021-05-01
err70
PREAI
errHerman, Laetitia; Todeschini, Anne-Laure; Veitia, Reiner A.
err分享
err收藏
Genomic exploration of the targets of FOXL2 and ESR2 unveils their implication in cell migration, invasion, and adhesion
errFASEB JOURNAL
IF4.2
err2021-03-22
err12
PREAI
errHerman, Laetitia; Legois, Berangere; Todeschini, Anne-Laure; Veitia, Reiner A.
err分享
err收藏
Insights into the pathogenicity of missense variants in the forkhead domain of FOX proteins underlying Mendelian disorders
errHUMAN GENETICS
IF3.6
err2021-02-27
err2
PREAI
errBermudez-Guzman, Luis; Veitia, Reiner A.
err分享
err收藏
Predictable increase in female reproductive window A simple model connecting age of reproduction, menopause, and longevity
errBIOESSAYS
IF2.7
err2021-02-11
err1
PREAI
errInnan, Hideki; Vaiman, Daniel; Veitia, Reiner A.
err分享
err收藏
A reply to: Longitudinal changes in the frequency of mosaic chromosome Y loss in peripheral blood cells of aging men varies profoundly between individuals
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2021-01-18
err0
errOAAI
errVeitia, Reiner A.
err分享
err收藏

研究方向

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合作学者
合作期刊
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David G. Huntsman
H 指数: 147 · 论文数: 1.1K
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H 指数: 141 · 论文数: 677
Y
Yves Van de Peer
H 指数: 133 · 论文数: 770
J
Jeroen Raes
H 指数: 127 · 论文数: 465
J
J. Beckmann
H 指数: 123 · 论文数: 883
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