Comparative ICE genomics: insights into the evolution of the SXT/R391 family of ICEs
Wozniak, Rachel A F, Fouts, Derrick E, Spagnoletti, Matteo, Colombo, Mauro M, Ceccarelli, Daniela, Garriss, Geneviève, Déry, Christine, Burrus, Vincent, Waldor, Matthew K
Published in PLoS genetics (01.12.2009)
Published in PLoS genetics (01.12.2009)
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Live births in women with recurrent hydatidiform mole and two NLRP7 mutations
Akoury, Elie, Gupta, Neerja, Bagga, Rashmi, Brown, Stephen, Déry, Christine, Kabra, Madhulika, Srinivasan, Radhika, Slim, Rima
Published in Reproductive biomedicine online (01.07.2015)
Published in Reproductive biomedicine online (01.07.2015)
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Comprehensive genotype–phenotype correlations between NLRP7 mutations and the balance between embryonic tissue differentiation and trophoblastic proliferation
Nguyen, Ngoc Minh Phuong, Zhang, Li, Reddy, Ramesh, Déry, Christine, Arseneau, Jocelyne, Cheung, Annie, Surti, Urvashi, Hoffner, Lori, Seoud, Muhieddine, Zaatari, Ghazi, Bagga, Rashmi, Srinivasan, Radhika, Coullin, Philippe, Ao, Asangla, Slim, Rima
Published in Journal of medical genetics (01.09.2014)
Published in Journal of medical genetics (01.09.2014)
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Comparative ICE Genomics: Insights into the Evolution of the SXT/R391 Family of ICEs: e1000786
Wozniak, Rachel AF, Fouts, Derrick E, Spagnoletti, Matteo, Colombo, Mauro M, Ceccarelli, Daniela, Garriss, Geneviève, Déry, Christine, Burrus, Vincent, Waldor, Matthew K
Published in PLoS genetics (01.12.2009)
Published in PLoS genetics (01.12.2009)
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Plasma p-tau217 predicts cognitive impairments up to ten years before onset in normal older adults
Yakoub, Yara, Gonzalez-Ortiz, Fernando, Ashton, Nicholas J, Déry, Christine, Strikwerda-Brown, Cherie, St-Onge, Frédéric, Ourry, Valentin, Schöll, Michael, Geddes, Maiya R, Ducharme, Simon, Montembeault, Maxime, Rosa-Neto, Pedro, Soucy, Jean-Paul, Breitner, John C S, Zetterberg, Henrik, Blennow, Kaj, Poirier, Judes, Villeneuve, Sylvia
Published in medRxiv : the preprint server for health sciences (09.05.2024)
Published in medRxiv : the preprint server for health sciences (09.05.2024)
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Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7
Reddy, Ramesh, Akoury, Elie, Phuong Nguyen, Ngoc Minh, Abdul-Rahman, Omar A, Dery, Christine, Gupta, Neerja, Daley, William P, Ao, Asangla, Landolsi, Hanene, Ann Fisher, Rosemary, Touitou, Isabelle, Slim, Rima
Published in European journal of human genetics : EJHG (01.09.2013)
Published in European journal of human genetics : EJHG (01.09.2013)
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Absence of KHDC3L mutations in Chinese patients with recurrent and sporadic hydatidiform moles
Zhao, Wei, Muhetaer, ALaNuEr, Luo, TengFei, Zhou, Wei, Qi, Cheng, Chen, XiaoDuan, Zhang, XiaoFei, Zhang, ZhiFen, Dery, Christine, Slim, Rima, Qian, JianHua
Published in Cancer genetics (01.09.2013)
Published in Cancer genetics (01.09.2013)
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