Tripathy, Ratna; Leca, Ines; van Dijk, Tessa; Weiss, Janneke; van Bon, Bregje W.; Sergaki, Maria Christina; Gstrein, Thomas; Breuss, Martin; Tian, Guoling; Bahi-Buisson, Nadia; Paciorkowski, Alexander R.; Pagnamenta, Alistair T.; Wenninger-Weinzierl, Andrea; Martinez-Reza, Maria Fernanda; Landler, Lukas; Lise, Stefano; Taylor, Jenny C.; Terrone, Gaetano; Vitiello, Giuseppina; Del Giudice, Ennio; Brunetti-Pierri, Nicola; D'Amico, Alessandra; Reymond, Alexandre; Voisin, Norine; Bernstein, Jonathan A.; Farrelly, Ellyn; Kini, Usha; Leonard, Thomas A.; Valence, Stephanie; Burglen, Lydie; Armstrong, Linlea; Hiatt, Susan M.; Cooper, Gregory M.; Aldinger, Kimberly A.; Dobyns, William B.; Mirzaa, Ghayda; Pierson, Tyler Mark; Baas, Frank; Chelly, Jamel; Cowan, Nicholas J.; Keays, David Anthony

Lidocaine is a nocebo treatment for trigeminally mediated magnetic orientation in birds

JOURNAL OF THE ROYAL SOCIETY INTERFACE

IF3.5

2018-08-0810

OAAI

Subcellular analysis of pigeon hair cells implicates vesicular trafficking in cuticulosome formation and maintenance

ELIFE

IF0

2017-11-1510

OAAI

Is magnetogenetics the new optogenetics?

EMBO JOURNAL

IF8.3

2017-05-2352

OAAI

Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability

HUMAN MOLECULAR GENETICS

IF3.2

2016-12-2317

OAAI

Mutations in the HECT domain of NEDD4L lead to AKT-mTOR pathway deregulation and cause periventricular nodular heterotopia

NATURE GENETICS

IF31.8

2016-10-0398

OAAI

Broix, Loic; Jagline, Helene; Ivanova, Ekaterina L.; Schmucker, Stephane; Drouot, Nathalie; Clayton-Smith, Jill; Pagnamenta, Alistair T.; Metcalfe, Kay A.; Isidor, Bertrand; Louvier, Ulrike Walther; Poduri, Annapurna; Taylor, Jenny C.; Tilly, Peggy; Poirier, Karine; Saillour, Yoann; Lebrun, Nicolas; Stemmelen, Tristan; Rudolf, Gabrielle; Muraca, Giuseppe; Saintpierre, Benjamin; Elmorjani, Adrienne; Moise, Martin; Weirauch, Nathalie Bednarek; Guerrini, Renzo; Boland, Anne; Olaso, Robert; Masson, Cecile; Tripathy, Ratna; Keays, David; Beldjord, Cherif; Nguyen, Laurent; Godin, Juliette; Kini, Usha; Nischke, Patrick; Deleuze, Jean-Francois; Bahi-Buisson, Nadia; Sumara, Izabela; Hinckelmann, Maria-Victoria; Chelly, Jamel

Mutations in the murine homologue of TUBB5 cause microcephaly by perturbing cell cycle progression and inducing p53-associated apoptosis

DEVELOPMENT

IF3.6

2016-01-0129

OAAI

Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2015-12-0171

OAAI

David A. Keays

个人简介

教育背景

工作经历

荣誉奖项

研究方向