Not logged in A Catalogue of Structural Variation across Ancestrally Diverse Asian Genomes Tan, Joanna Hui Juan; Li, Zhihui; Porta, Mar Gonzalez; Rajaby, Ramesh; Lim, Weng Khong; Tan, Ye An; Jimenez, Rodrigo Toro; Teo, Renyi; Hebrard, Maxime; Ow, Jack Ling; Ang, Shimin; Jeyakani, Justin; Chong, Yap Seng; Lim, Tock Han; Goh, Liuh Ling; Tham, Yih Chung; Leong, Khai Pang; Chin, Calvin Woon Loong; Davila, Sonia; Karnani, Neerja; Cheng, Ching-Yu; Chambers, John; Tai, E. Shyong; Liu, Jianjun; Sim, Xueling; Sung, Wing Kin; Prabhakar, Shyam; Tan, Patrick; Bertin, Nicolas Share Save
SMARCAL1 is a dual regulator of innate immune signaling and PD-L1 expression that promotes tumor immune evasion Leuzzi, Giuseppe; Vasciaveo, Alessandro; Taglialatela, Angelo; Chen, Xiao; Firestone, Tessa M.; Hickman, Allison R.; Mao, Wendy; Thakar, Tanay; Vaitsiankova, Alina; Huang, Jen-Wei; Cuella-Martin, Raquel; Hayward, Samuel B.; Kesner, Jordan S.; Ghasemzadeh, Ali; Nambiar, Tarun S.; Ho, Patricia; Rialdi, Alexander; Hebrard, Maxime; Li, Yinglu; Gao, Jinmei; Gopinath, Saarang; Adeleke, Oluwatobi A.; Venters, Bryan; Drake, Charles G.; Baer, Richard; Izar, Benjamin; Guccione, Ernesto; Keogh, Michael-Christopher; Guerois, Raphael; Sun, Lu; Lu, Chao; Califano, Andrea; Ciccia, Alberto Share Save
The Singapore National Precision Medicine Strategy Wong, Eleanor; Bertin, Nicolas; Hebrard, Maxime; Tirado-Magallanes, Roberto; Bellis, Claire; Lim, Weng Khong; Chua, Chee Yong; Tong, Philomena Mei Lin; Chua, Raymond; Mak, Kenneth; Lim, Tit Meng; Cheong, Wei Yang; Thien, Kwee Eng; Goh, Khean Teik; Chai, Jin-Fang; Lee, Jimmy; Sung, Joseph Jao-Yiu; Wong, Tien Yin; Chin, Calvin Woon Loong D.; Gluckman, Peter; Goh, Liuh Ling; Ban, Kenneth Hon Kim; Tan, Tin Wee M.; Van Dam, Rob M.; Teo, Yik Ying; Loh, Marie; Eillot, Paul; Lee, Eng Sing; Ngeow, Joanne; Riboli, Elio; Dalan, Rinkoo; Kassam, Irfahan; Lakshmanan, Lakshmi Narayanan; Lim, Tock Han; Ng, Hong Kiat; Mina, Theresia; Tay, Darwin; Sabanayagam, Charumathi; Tham, Yih Chung; Rim, Tyler; Aung, Tin; Chee, Miao Ling; Li, Hengtong; Chee, Miao Li; Yeo, Khung Keong; Cook, Stuart Alexander; Pua, Chee Jian; Yang, Chengxi; Chong, Yap Seng; Eriksson, Johan Gunnar; Tan, Kok Hian; Yap, Fabian; Lim, Chia Wei; Tsai, Pi Kuang; Chew, Wen Jie; Sim, Wey Ching; Toh, Li-xian Grace; Lin, Clarabelle Bitong; Sia, Yee Yen; Koh, Tat Hung; Meah, Wee Yang; Tan, Joanna Hui Juan; Jeyakani, Justin; Ow, Jack; Ang, Shimin; Malik, Ashar J.; Kenanov, Dimitar; Sim, Xueling; Cheng, Ching-Yu; Davila, Sonia; Karnani, Neerja; Leong, Khai Pang; Liu, Jianjun; Prabhakar, Shyam; Maurer-Stroh, Sebastian; Verma, Chandra Shekhar; Krishnaswamy, Pavitra; Goh, Rick Siow Mong; Chia, Irenaeus; Ho, Clarissa; Low, Doreen; Virabhak, Suchin; Yong, Jacklyn; Zheng, Weiling; Seow, Shih Wee; Seck, Yee Kwang; Koh, Mingshi; Chambers, John C.; Tai, E. Shyong; Tan, Patrick Share Save
Analysis of clinically relevant variants from ancestrally diverse Asian genomes Chan, Sock Hoai; Bylstra, Yasmin; Teo, Jing Xian; Kuan, Jyn Ling; Bertin, Nicolas; Gonzalez-Porta, Mar; Hebrard, Maxime; Tirado-Magallanes, Roberto; Tan, Joanna Hui Juan; Jeyakani, Justin; Li, Zhihui; Chai, Jin Fang; Chong, Yap Seng; Davila, Sonia; Goh, Liuh Ling; Lee, Eng Sing; Wong, Eleanor; Wong, Tien Yin; Prabhakar, Shyam; Liu, Jianjun; Cheng, Ching-Yu; Eisenhaber, Birgit; Karnani, Neerja; Leong, Khai Pang; Sim, Xueling; Yeo, Khung Keong; Chambers, John C.; Tai, E-Shyong; Tan, Patrick; Jamuar, Saumya S.; Ngeow, Joanne; Lim, Weng Khong Share Save
EHMT2 epigenetically suppresses Wnt signaling and is a potential target in embryonal rhabdomyosarcoma Pal, Ananya; Leung, Jia Yu; Ang, Gareth Chin Khye; Rao, Vinay Kumar; Pignata, Luca; Lim, Huey Jin; Hebrard, Maxime; Chang, Kenneth T. E.; Lee, Victor K. M.; Guccione, Ernesto; Taneja, Reshma Share Save
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Population genomics of picophytoplankton unveils novel chromosome hypervariability Blanc-Mathieu, Romain; Krasovec, Marc; Hebrard, Maxime; Yau, Sheree; Desgranges, Elodie; Martin, Joel; Schackwitz, Wendy; Kuo, Alan; Salin, Gerald; Donnadieu, Cecile; Desdevises, Yves; Sanchez-Ferandin, Sophie; Moreau, Herve; Rivals, Eric; Grigoriev, Igor V.; Grimsley, Nigel; Eyre-Walker, Adam; Piganeau, Gwenael Share Save
Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies Angebault, Claire; Guichet, Pierre-Olivier; Talmat-Amar, Yasmina; Charif, Majida; Gerber, Sylvie; Fares-Taie, Lucas; Gueguen, Naig; Halloyn, Francois; Moore, David; Amati-Bonneau, Patrizia; Manes, Gael; Hebrard, Maxime; Bocquet, Beatrice; Quiles, Melanie; Piro-Megy, Camille; Teigell, Marisa; Delettre, Cecile; Rossel, Mireille; Meunier, Isabelle; Preising, Markus; Lorenz, Birgit; Carelli, Valerio; Chinnery, Patrick F.; Yu-Wai-Man, Patrick; Kaplan, Josseline; Roubertie, Agathe; Barakat, Abdelhamid; Bonneau, Dominique; Reynier, Pascal; Rozet, Jean-Michel; Bomont, Pascale; Hamel, Christian P.; Lenaers, Guy Share Save
Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies (vol 97, pg 754, 2015) Angebault, Claire; Guichet, Pierre-Olivier; Talmat-Amar, Yasmina; Charif, Majida; Gerber, Sylvie; Fares-Taie, Lucas; Gueguen, Naig; Halloy, Francois; Moore, David; Amati-Bonneau, Patrizia; Manes, Gael; Hebrard, Maxime; Bocquet, Beatrice; Quiles, Melanie; Piro-Megy, Camille; Teigell, Marisa; Delettre, Cecile; Rossel, Mireille; Meunier, Isabelle; Preising, Markus; Lorenz, Birgit; Carelli, Valerio; Chinnery, Patrick F.; Yu-Wai-Man, Patrick; Kaplan, Josseline; Roubertie, Agathe; Barakat, Abdelhamid; Bonneau, Dominique; Reynier, Pascal; Rozet, Jean-Michel; Bomont, Pascale; Hamel, Christian P.; Lenaers, Guy Share Save
Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability Angebault, Claire; Charif, Majida; Guegen, Naig; Piro-Megy, Camille; de Camaret, Benedicte Mousson; Procaccio, Vincent; Guichet, Pierre-Olivier; Hebrard, Maxime; Manes, Gael; Leboucq, Nicolas; Rivier, Francois; Hamel, Christian P.; Lenaers, Guy; Roubertie, Agathe Share Save
Mutations in IMPG1 Cause Vitelliform Macular Dystrophies Manes, Gael; Meunier, Isabelle; Avila-Fernandez, Almudena; Banfi, Sandro; Le Meur, Guylene; Zanlonghi, Xavier; Corton, Marta; Simonelli, Francesca; Brabet, Philippe; Labesse, Gilles; Audo, Isabelle; Mohand-Said, Saddek; Zeitz, Christina; Sahel, Jose-Alain; Weber, Michel; Dollfus, Helene; Dhaenens, Claire-Marie; Allorge, Delphine; De Baere, Elfride; Koenekoop, Robert K.; Kohl, Susanne; Cremers, Frans P. M.; Hollyfield, Joe G.; Senechal, Audrey; Hebrard, Maxime; Bocquet, Beatrice; Ayuso Garcia, Carmen; Hamel, Christian P. Share Save
Combining gene mapping and phenotype assessment for fast mutation finding in non-consanguineous autosomal recessive retinitis pigmentosa families Hebrard, Maxime; Manes, Gael; Bocquet, Beatrice; Meunier, Isabelle; Coustes-Chazalette, Delphine; Herald, Emilie; Senechal, Audrey; Bolland-Auge, Anne; Zelenika, Diana; Hamel, Christian P. Share Save
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