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

SURFBAT: a surrogate family based association test building on large imputation reference panels

SURFBAT:一种基于大型插补参考面板的替代家庭关联性检验

Herzig, Anthony F; Rubinacci, Simone; Marenne, Gaëlle; Perdry, Hervé; Deleuze, Jean-François; Dina, Christian; Barc, Julien; Redon, Richard; Delaneau, Olivier; Génin, Emmanuelle

Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score

检测编码和非编码基因组中罕见变异的关联性:RAVA-FIRST,一种基于CADD有害性评分的新方法

Bocher, Ozvan; Ludwig, Thomas E; Oglobinsky, Marie-Sophie; Marenne, Gaëlle; Deleuze, Jean-François; Suryakant, Suryakant; Odeberg, Jacob; Morange, Pierre-Emmanuel; Trégouët, David-Alexandre; Perdry, Hervé; Génin, Emmanuelle

Moment estimators of relatedness from low-depth whole-genome sequencing data

基于低深度全基因组测序数据的亲缘关系矩估计

Herzig, Anthony F; Ciullo, M; Leutenegger, A-L; Perdry, H

Extension of SKAT to multi-category phenotypes through a geometrical interpretation

通过几何解释将SKAT扩展到多类别表型

Bocher, Ozvan; Marenne, Gaelle; Tournier-Lasserve, Elisabeth; Génin, Emmanuelle; Perdry, Hervé

The hCOMET project: International database comparison of results with the comet assay in human biomonitoring. Baseline frequency of DNA damage and effect of main confounders

hCOMET项目:利用彗星试验进行人体生物监测的国际数据库结果比较。DNA损伤的基线频率及主要混杂因素的影响

Milić, Mirta; Ceppi, Marcello; Bruzzone, Marco; Azqueta, Amaya; Brunborg, Gunnar; Godschalk, Roger; Koppen, Gudrun; Langie, Sabine; Møller, Peter; Teixeira, João Paulo; Alija, Avdulla; Anderson, Diana; Andrade, Vanessa; Andreoli, Cristina; Asllani, Fisnik; Bangkoglu, Ezgi Eyluel; Barančoková, Magdalena; Basaran, Nursen; Boutet-Robinet, Elisa; Buschini, Annamaria; Cavallo, Delia; Costa Pereira, Cristiana; Costa, Carla; Costa, Solange; Da Silva, Juliana; Del Boˊ, Cristian; Dimitrijević Srećković, Vesna; Djelić, Ninoslav; Dobrzyńska, Malgorzata; Duračková, Zdenka; Dvořáková, Monika; Gajski, Goran; Galati, Serena; García Lima, Omar; Giovannelli, Lisa; Goroshinskaya, Irina A; Grindel, Annemarie; Gutzkow, Kristine B; Hernández, Alba; Hernández, Carlos; Holven, Kirsten B; Ibero-Baraibar, Idoia; Ottestad, Inger; Kadioglu, Ela; Kažimirová, Alena; Kuznetsova, Elena; Ladeira, Carina; Laffon, Blanca; Lamonaca, Palma; Lebailly, Pierre; Louro, Henriqueta; Mandina Cardoso, Tania; Marcon, Francesca; Marcos, Ricard; Moretti, Massimo; Moretti, Silvia; Najafzadeh, Mojgan; Nemeth, Zsuzsanna; Neri, Monica; Novotna, Bozena; Orlow, Irene; Paduchova, Zuzana; Pastor, Susana; Perdry, Hervé; Spremo-Potparević, Biljana; Ramadhani, Dwi; Riso, Patrizia; Rohr, Paula; Rojas, Emilio; Rossner, Pavel; Safar, Anna; Sardas, Semra; Silva, Maria João; Sirota, Nikolay; Smolkova, Bozena; Staruchova, Marta; Stetina, Rudolf; Stopper, Helga; Surikova, Ekaterina I; Ulven, Stine M; Ursini, Cinzia Lucia; Valdiglesias, Vanessa; Valverde, Mahara; Vodicka, Pavel; Volkovova, Katarina; Wagner, Karl-Heinz; Živković, Lada; Dušinská, Maria; Collins, Andrew R; Bonassi, Stefano

Mixed logistic regression in genome-wide association studies

全基因组关联研究中的混合逻辑回归

Milet, Jacqueline; Courtin, David; Garcia, André; Perdry, Hervé

Adipose Tissue Properties in Tumor-Bearing Breasts

肿瘤乳腺脂肪组织的特性

Miran, Isabelle; Scherer, Dominique; Ostyn, Pauline; Mazouni, Chafika; Drusch, Françoise; Bernard, Marine; Louvet, Emilie; Adam, Julien; Mathieu, Marie-Christine; Haffa, Mariam; Antignac, Jean-Philippe; Le Bizec, Bruno; Vielh, Philippe; Dessen, Philippe; Perdry, Hervé; Delaloge, Suzette; Feunteun, Jean

Detecting the dominance component of heritability in isolated and outbred human populations

检测孤立且近亲繁殖的人类群体中遗传力的显性成分

Herzig, Anthony F; Nutile, Teresa; Ruggiero, Daniela; Ciullo, Marina; Perdry, Hervé; Leutenegger, Anne-Louise

TNFSF10/TRAIL regulates human T4 effector memory lymphocyte radiosensitivity and predicts radiation-induced acute and subacute dermatitis

TNFSF10/TRAIL 调节人类 T4 效应记忆淋巴细胞放射敏感性并预测放射引起的急性和亚急性皮炎

Jan Baijer, Nathalie Déchamps, Hervé Perdry, Pablo Morales, Sarah Kerns, Alexandre Vasilescu, Sylvain Baulande, David Azria, Paul Henri Roméo, Annette Schmitz

Where is the causal variant? On the advantage of the family design over the case-control design in genetic association studies

致病变异在哪里?论遗传关联研究中家庭设计相对于病例对照设计的优势

Dandine-Roulland, Claire; Perdry, Hervé