Christopher T Gordon (Christopher Gordon, C T Gordon)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 25

Top Venues

Nature communications

Proceedings of the National Academy of Sciences of the United States of America

Nature genetics

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Elise Pisan, Chiara De Luca, Francesco Brancati, Rossana Sanchez Russo, Dong Li, Elizabeth Joyce Bhoj, Tara Wenger, Ashish Marwaha, Nicole Johnson, Claire Beneteau, Elise Brischoux-Boucher, Gunnar Houge, Julie Paulsen, Trine Bjørg Hammer, Jakob Ek, Daniela Schweitzer, Bianca E Russell, Marina Dutra-Clarke, Stanley Nelson, Emilie D Douine, Rosario I Corona, Tracy Dudding, Hannah Thomson, Karen Low, Newell Belnap, Maria Iascone, Manuela Priolo, Diana Carli, Alessandro Mussa, Emilia K Bijlsma, Nathan Kopp, Jean-Philippe Jais, Jeanne Amiel, Christopher T Gordon
The spectrum of heart defects in the TRAF7 -related multiple congenital anomalies-intellectual disability syndrome. Proceedings of the National Academy of Sciences of the United States of America 121 (12) (2024)
Elizabeth A Werren, Geneva R LaForce, Anshika Srivastava, Delia R Perillo, Shaokun Li, Katherine Johnson, Safa Baris, Brandon Berger, Samantha L Regan, Christian D Pfennig, Sonja de Munnik, Rolph Pfundt, Malavika Hebbar, Raúl Jimenez-Heredia, Elif Karakoc-Aydiner, Ahmet Ozen, Jasmin Dmytrus, Ana Krolo, Ken Corning, E J Prijoles, Raymond J Louie, Robert Roger Lebel, Thuy-Linh Le, Jeanne Amiel, Christopher T Gordon, Kaan Boztug, Katta Mohan Girisha, Anju Shukla, Stephanie L Bielas, Ashleigh E Schaffer
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome. Nature communications 15 (1) (2024)
Elizabeth A Werren, Geneva R LaForce, Anshika Srivastava, Delia R Perillo, Shaokun Li, Katherine Johnson, Safa Baris, Brandon Berger, Samantha L Regan, Christian D Pfennig, Sonja de Munnik, Rolph Pfundt, Malavika Hebbar, Raúl Jimenez-Heredia, Elif Karakoc-Aydiner, Ahmet Ozen, Jasmin Dmytrus, Ana Krolo, Ken Corning, E J Prijoles, Raymond J Louie, Robert Roger Lebel, Thuy-Linh Le, Jeanne Amiel, Christopher T Gordon, Kaan Boztug, Katta Mohan Girisha, Anju Shukla, Stephanie L Bielas, Ashleigh E Schaffer
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome. Nature communications 15 (1) (2024)
Elise Pisan, Chiara De Luca, Francesco Brancati, Rossana Sanchez Russo, Dong Li, Elizabeth Joyce Bhoj, Tara Wenger, Ashish Marwaha, Nicole Johnson, Claire Beneteau, Elise Brischoux-Boucher, Gunnar Houge, Julie Paulsen, Trine Bjørg Hammer, Jakob Ek, Daniela Schweitzer, Bianca E Russell, Marina Dutra-Clarke, Stanley Nelson, Emilie D Douine, Rosario I Corona, Tracy Dudding, Hannah Thomson, Karen Low, Newell Belnap, Maria Iascone, Manuela Priolo, Diana Carli, Alessandro Mussa, Emilia K Bijlsma, Nathan Kopp, Jean-Philippe Jais, Jeanne Amiel, Christopher T Gordon
The spectrum of heart defects in the TRAF7 -related multiple congenital anomalies-intellectual disability syndrome. Proceedings of the National Academy of Sciences of the United States of America 121 (12) (2024)
Elise Pisan, Chiara De Luca, Francesco Brancati, Rossana Sanchez Russo, Dong Li, Elizabeth Joyce Bhoj, Tara Wenger, Ashish Marwaha, Nicole Johnson, Claire Beneteau, Elise Brischoux-Boucher, Gunnar Houge, Julie Paulsen, Trine Bjørg Hammer, Jakob Ek, Daniela Schweitzer, Bianca E Russell, Marina Dutra-Clarke, Stanley Nelson, Emilie D Douine, Rosario I Corona, Tracy Dudding, Hannah Thomson, Karen Low, Newell Belnap, Maria Iascone, Manuela Priolo, Diana Carli, Alessandro Mussa, Emilia K Bijlsma, Nathan Kopp, Jean-Philippe Jais, Jeanne Amiel, Christopher T Gordon
The spectrum of heart defects in the TRAF7 -related multiple congenital anomalies-intellectual disability syndrome. Proceedings of the National Academy of Sciences of the United States of America 121 (12) (2024)
Elizabeth A Werren, Geneva R LaForce, Anshika Srivastava, Delia R Perillo, Shaokun Li, Katherine Johnson, Safa Baris, Brandon Berger, Samantha L Regan, Christian D Pfennig, Sonja de Munnik, Rolph Pfundt, Malavika Hebbar, Raúl Jimenez-Heredia, Elif Karakoc-Aydiner, Ahmet Ozen, Jasmin Dmytrus, Ana Krolo, Ken Corning, E J Prijoles, Raymond J Louie, Robert Roger Lebel, Thuy-Linh Le, Jeanne Amiel, Christopher T Gordon, Kaan Boztug, Katta Mohan Girisha, Anju Shukla, Stephanie L Bielas, Ashleigh E Schaffer
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome. Nature communications 15 (1) (2024)
Elizabeth A Werren, Geneva R LaForce, Anshika Srivastava, Delia R Perillo, Shaokun Li, Katherine Johnson, Safa Baris, Brandon Berger, Samantha L Regan, Christian D Pfennig, Sonja de Munnik, Rolph Pfundt, Malavika Hebbar, Raúl Jimenez-Heredia, Elif Karakoc-Aydiner, Ahmet Ozen, Jasmin Dmytrus, Ana Krolo, Ken Corning, E J Prijoles, Raymond J Louie, Robert Roger Lebel, Thuy-Linh Le, Jeanne Amiel, Christopher T Gordon, Kaan Boztug, Katta Mohan Girisha, Anju Shukla, Stephanie L Bielas, Ashleigh E Schaffer
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome. Nature communications 15 (1) (2024)
Elizabeth A Werren, Geneva R LaForce, Anshika Srivastava, Delia R Perillo, Shaokun Li, Katherine Johnson, Safa Baris, Brandon Berger, Samantha L Regan, Christian D Pfennig, Sonja de Munnik, Rolph Pfundt, Malavika Hebbar, Raúl Jimenez-Heredia, Elif Karakoc-Aydiner, Ahmet Ozen, Jasmin Dmytrus, Ana Krolo, Ken Corning, E J Prijoles, Raymond J Louie, Robert Roger Lebel, Thuy-Linh Le, Jeanne Amiel, Christopher T Gordon, Kaan Boztug, Katta Mohan Girisha, Anju Shukla, Stephanie L Bielas, Ashleigh E Schaffer
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome. Nature communications 15 (1) (2024)
Valeria Agostini, Aude Tessier, Nabila Djaziri, Roman Hossein Khonsari, Eva Galliani, Yukiko Kurihara, Masahiko Honda, Hiroki Kurihara, Kyoko Hidaka, Gokhan Tuncbilek, Arnaud Picard, Ersoy Konas, Jeanne Amiel, Christopher T Gordon
Biallelic truncating variants in VGLL2 cause syngnathia in humans. Journal of medical genetics (2023)
Elizabeth Werren, Geneva LaForce, Anshika Srivast, Delia Perillo, Katherine Johnson, Brandon Berger, Samantha Regan, Christian Pfennig, Safa Baris, Sonja de Munnik, Rolph Pfundt, Malavika Hebbar, Raul Jimenez Heredia, Elif Karakoc-Aydiner, Ahmet Ozen, Jasmin Dmytrus, Ana Krolo, Ken Corning, Eloise Prijoles, Raymond Louie, Robert Lebel, Thuy-Linh Le, Jeanne Amiel, Christopher T Gordon, Kaan Boztug, Katta Mohan Girisha, Anju Shukla, Stephanie L Bielas, Ashleigh E Schaffer
Mechanisms of mRNA processing defects in inherited THOC6 intellectual disability syndrome. Research square (2023)
Mythily Ganapathi, Leticia S Matsuoka, Michael March, Dong Li, Elly Brokamp, Sara Benito-Sanz, Susan M White, Katherine Lachlan, Priyanka Ahimaz, Anshuman Sewda, Lisa Bastarache, Amanda Thomas-Wilson, Joan M Stoler, Nuria C Bramswig, Júlia Baptista, Karen L Stals, Florence Demurger, Benjamin Cogné, Bertrand Isidor, Maria Francesca Bedeschi, Angela Peron, Jeanne Amiel, Elaine H Zackai, John P Schacht, Alejandro D Iglesias, Jenny Morton, Ariane Schmetz, null null, Verónica Seidel, Stephanie Lucia, Stephanie M Baskin, Isabelle Thiffault, Joy D Cogan, Christopher T Gordon, Wendy K Chung, Sarah Bowdin, Elizabeth Joyce Bhoj
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays. European journal of human genetics : EJHG (2023)
Anne Guimier, Loïc Pontual, Stephen R Braddock, Erin Torti, Luis A Pérez-Jurado, Patricia Muñoz-Cabello, Montserrat Arumí, Kristin G Monaghan, Hane Lee, Lee-Kai Wang, Ilina D Pluym, Sally Ann Lynch, Karen Stals, Sian Ellard, Cécile Muller, Lucile Houyel, Laurence Cohen, Stanislas Lyonnet, Fanny Bajolle, Jeanne Amiel, Christopher T Gordon
Biallelic alterations in PLXND1 cause common arterial trunk and other cardiac malformations in humans. Human molecular genetics (2022)
Víctor Faundes, Martin D Jennings, Siobhan Crilly, Sarah Legraie, Sarah E Withers, Sara Cuvertino, Sally J Davies, Andrew G L Douglas, Andrew E Fry, Victoria Harrison, Jeanne Amiel, Daphné Lehalle, William G Newman, Patricia Newkirk, Judith Ranells, Miranda Splitt, Laura Ann Cross, Carol J Saunders, Bonnie R Sullivan, Jorge L Granadillo, Christopher T Gordon, Paul R Kasher, Graham D Pavitt, Siddharth Banka
Impaired eIF5A function causes a Mendelian disorder that is partially rescued in model systems by spermidine. Nature communications 12 (1) (2021)
Emmanuelle Szenker-Ravi, Tim Ott, Muznah Khatoo, Anne Moreau de Bellaing, Wei Xuan Goh, Yan Ling Chong, Anja Beckers, Darshini Kannesan, Guillaume Louvel, Priyanka Anujan, Vydianathan Ravi, Carine Bonnard, Sebastien Moutton, Patric Schoen, Mélanie Fradin, Estelle Colin, Andre Megarbane, Linda Daou, Ghassan Chehab, Sylvie Di Filippo, Caroline Rooryck, Jean François Deleuze, Anne Boland-Auge, Nicolas Arribard, Rukiye Eker, Sumanty Tohari, Alvin Yu-Jin Ng, Marlène Rio, Chun Teck Lim, Birgit Eisenhaber, Frank Eisenhaber, Byrappa Venkatesh, Jeanne Amiel, Hugues Roest Crollius, Christopher T Gordon, Achim Gossler, Sudipto Roy, Tania Attie-Bitach, Martin Blum, Patrice Bouvagnet, Bruno Reversade
Discovery of a genetic module essential for assigning left-right asymmetry in humans and ancestral vertebrates. Nature genetics 54 (1) (2021)
Laura Castilla-Vallmanya, Kaja K Selmer, Clémantine Dimartino, Raquel Rabionet, Bernardo Blanco-Sánchez, Sandra Yang, Margot R F Reijnders, Antonie J van Essen, Myriam Oufadem, Magnus D Vigeland, Barbro Stadheim, Gunnar Houge, Helen Cox, Helen Kingston, Jill Clayton-Smith, Jeffrey W Innis, Maria Iascone, Anna Cereda, Sara Gabbiadini, Wendy K Chung, Victoria Sanders, Joel Charrow, Emily Bryant, John Millichap, Antonio Vitobello, Christel Thauvin, Frederic Tran Mau-Them, Laurence Faivre, Gaetan Lesca, Audrey Labalme, Christelle Rougeot, Nicolas Chatron, Damien Sanlaville, Katherine M Christensen, Amelia Kirby, Raymond Lewandowski, Rachel Gannaway, Maha Aly, Anna Lehman, Lorne Clarke, Luitgard Graul-Neumann, Christiane Zweier, Davor Lessel, Bernarda Lozic, Ingvild Aukrust, Ryan Peretz, Robert Stratton, Thomas Smol, Anne Dieux-Coëslier, Joanna Meira, Elizabeth Wohler, Nara Sobreira, Erin M Beaver, Jennifer Heeley, Lauren C Briere, Frances A High, David A Sweetser, Melissa A Walker, Catherine E Keegan, Parul Jayakar, Marwan Shinawi, Wilhelmina S Kerstjens-Frederikse, Dawn L Earl, Victoria M Siu, Emma Reesor, Tony Yao, Robert A Hegele, Olena M Vaske, Shannon Rego, null null, Kevin A Shapiro, Brian Wong, Michael J Gambello, Marie McDonald, Danielle Karlowicz, Roberto Colombo, Alessandro Serretti, Lynn Pais, Anne O'Donnell-Luria, Alison Wray, Simon Sadedin, Belinda Chong, Tiong Y Tan, John Christodoulou, Susan M White, Anne Slavotinek, Deborah Barbouth, Dayna Morel Swols, Mélanie Parisot, Christine Bole-Feysot, Patrick Nitschké, Véronique Pingault, Arnold Munnich, Megan T Cho, Valérie Cormier-Daire, Susanna Balcells, Stanislas Lyonnet, Daniel Grinberg, Jeanne Amiel, Roser Urreizti, Christopher T Gordon
Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7. Genetics in medicine : official journal of the American College of Medical Genetics 22 (7) (2020)
Huw B Thomas, Katherine A Wood, Weronika A Buczek, Christopher T Gordon, Véronique Pingault, Tania Attie-Bitach, Kathryn E Hentges, Vinod C Varghese, Jeanne Amiel, William G Newman, Raymond T O'Keefe
EFTUD2 missense variants disrupt protein function and splicing in mandibulofacial dysostosis Guion-Almeida type. Human mutation 41 (8) (2020)
Caroline Alby, Lucile Boutaud, Bettina Bessières, Valérie Serre, Marlene Rio, Valerie Cormier-Daire, Judith de Oliveira, Amale Ichkou, Linda Mouthon, Christopher T Gordon, Maryse Bonnière, Charlotte Mechler, Patrick Nitschke, Christine Bole, Stanislas Lyonnet, Nadia Bahi-Buisson, Nathalie Boddaert, Laurence Colleaux, Philippe Roth, Yves Ville, Michel Vekemans, Féréchté Encha-Razavi, Tania Attié-Bitach, Sophie Thomas
Novel de novo ZBTB20 mutations in three cases with Primrose syndrome and constant corpus callosum anomalies. American journal of medical genetics. Part A 176 (5) (2019)
Johanne Dubail, Céline Huber, Sandrine Chantepie, Stephan Sonntag, Beyhan Tüysüz, Ercan Mihci, Christopher T Gordon, Elisabeth Steichen-Gersdorf, Jeanne Amiel, Banu Nur, Irene Stolte-Dijkstra, Albertien M van Eerde, Koen L van Gassen, Corstiaan C Breugem, Alexander Stegmann, Caroline Lekszas, Reza Maroofian, Ehsan Ghayoor Karimiani, Arnaud Bruneel, Nathalie Seta, Arnold Munnich, Dulce Papy-Garcia, Muriel De La Dure-Molla, Valérie Cormier-Daire
SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects. Nature communications 9 (1) (2018)
Jean-Luc Alessandri, Christopher T Gordon, Marie-Line Jacquemont, Nicolas Gruchy, Norbert F Ajeawung, Guillaume Benoist, Myriam Oufadem, Asma Chebil, Yannis Duffourd, Coralie Dumont, Marion Gérard, Paul Kuentz, Thibaud Jouan, Francesca Filippini, Thi Tuyet Mai Nguyen, Olivier Alibeu, Christine Bole-Feysot, Patrick Nitschké, Asma Omarjee, Duksha Ramful, Hanitra Randrianaivo, Bérénice Doray, Laurence Faivre, Jeanne Amiel, Philippe M Campeau, Julien Thevenon
Recessive loss of function PIGN alleles, including an intragenic deletion with founder effect in La Réunion Island, in patients with Fryns syndrome. European journal of human genetics : EJHG 26 (3) (2018)
Christopher T Gordon, Maya Chopra, Myriam Oufadem, Olivier Alibeu, Marc Bras, Nathalie Boddaert, Christine Bole-Feysot, Patrick Nitschké, Véronique Abadie, Stanislas Lyonnet, Jeanne Amiel
MED13L loss-of-function variants in two patients with syndromic Pierre Robin sequence. American journal of medical genetics. Part A 176 (1) (2017)
Christopher T Gordon, Shifeng Xue, Gökhan Yigit, Hicham Filali, Kelan Chen, Nadine Rosin, Koh-Ichiro Yoshiura, Myriam Oufadem, Tamara J Beck, Ruth McGowan, Alex C Magee, Janine Altmüller, Camille Dion, Holger Thiele, Alexandra D Gurzau, Peter Nürnberg, Dieter Meschede, Wolfgang Mühlbauer, Nobuhiko Okamoto, Vinod Varghese, Rachel Irving, Sabine Sigaudy, Denise Williams, Syed Faisal Ahmed, Carine Bonnard, Mung Kei Kong, Ilham Ratbi, Nawfal Fejjal, Meriem Fikri, Siham Chafai Elalaoui, Hallvard Reigstad, Christine Bole-Feysot, Patrick Nitschké, Nicola Ragge, Nicolas Lévy, Gökhan Tunçbilek, Audrey S M Teo, Michael L Cunningham, Abdelaziz Sefiani, Hülya Kayserili, James M Murphy, Chalermpong Chatdokmaiprai, Axel Maximilian Hillmer, Duangrurdee Wattanasirichaigoon, Stanislas Lyonnet, Frédérique Magdinier, Asif Javed, Marnie E Blewitt, Jeanne Amiel, Bernd Wollnik, Bruno Reversade
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development. Nature genetics 49 (2) (2017)
Christopher T Gordon, Aude Tessier, Z Demir, A Goldenberg, M Oufadem, N Voisin, V Pingault, Thierry Bienvenu, S Lyonnet, L de Pontual, J Amiel
The association of severe encephalopathy and question mark ear is highly suggestive of loss of MEF2C function. Clinical genetics 93 (2) (2017)
Elvira Di Pasquo, Jeanne Amiel, Philippe Roth, Valérie Malan, Katia Lind, Christel Chalouhi, Véronique Soupre, Christopher T Gordon, Stanislas Lyonnet, Laurent J Salomon, Véronique Abadie
Efficiency of prenatal diagnosis in Pierre Robin sequence. Prenatal diagnosis 37 (11) (2017)
Anne Guimier, George C Gabriel, Fanny Bajolle, Michael Tsang, Hui Liu, Aaron Noll, Molly Schwartz, Rajae El Malti, Laurie D Smith, Nikolai T Klena, Gina Jimenez, Neil A Miller, Myriam Oufadem, Anne Moreau de Bellaing, Hisato Yagi, Carol J Saunders, Candice N Baker, Sylvie Di Filippo, Kevin A Peterson, Isabelle Thiffault, Christine Bole-Feysot, Linda D Cooley, Emily G Farrow, Cécile Masson, Patric Schoen, Jean-François Deleuze, Patrick Nitschké, Stanislas Lyonnet, Loic de Pontual, Stephen A Murray, Damien Bonnet, Stephen F Kingsmore, Jeanne Amiel, Patrice Bouvagnet, Cecilia W Lo, Christopher T Gordon
MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates. Nature genetics 47 (11) (2015)
D Lehalle, D Wieczorek, R M Zechi-Ceide, M R Passos-Bueno, S Lyonnet, J Amiel, Christopher T Gordon
A review of craniofacial disorders caused by spliceosomal defects. Clinical genetics 88 (5) (2015)

Christopher T Gordon.css-eqlu8i{font-size:small;padding-left:4px;} (Christopher Gordon, C T Gordon)

Publication Activity (10 Years)

Top Topics

Top Venues

Christopher T Gordon (Christopher Gordon, C T Gordon)