Joseph G Gleeson

ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 21

Top Venues

Nature genetics

European journal of human genetics : EJHG

Nature biotechnology

Nature

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

Publications

Changuk Chung, Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels, H Westley Phillips, Zhen Li, Ashley P L Marsh, Martin W Breuss, Laurel L Ball, Camila Araújo Bernardino Garcia, Renee D George, Jing Gu, Mingchu Xu, Chelsea Barrows, Kiely N James, Valentina Stanley, Anna S Nidhiry, Sami Khoury, Gabrielle Howe, Emily Riley, Xin Xu, Brett Copeland, Yifan Wang, Se-Hoon Kim, Hoon-Chul Kang, Andreas Schulze-Bonhage, Carola A Haas, Horst Urbach, Marco Prinz, David D Limbrick, Christina A Gurnett, Matthew D Smyth, Shifteh Sattar, Mark Nespeca, David D Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin-Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Wilson Araújo da Silva Junior, Helio R Machado, Gary W Mathern, Alexej Abyzov, Sara Baldassari, Stéphanie Baulac, null null, null null, Joseph G Gleeson
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nature genetics 55 (2) (2023)
Changuk Chung, Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels, H Westley Phillips, Zhen Li, Ashley P L Marsh, Martin W Breuss, Laurel L Ball, Camila Araújo Bernardino Garcia, Renee D George, Jing Gu, Mingchu Xu, Chelsea Barrows, Kiely N James, Valentina Stanley, Anna S Nidhiry, Sami Khoury, Gabrielle Howe, Emily Riley, Xin Xu, Brett Copeland, Yifan Wang, Se-Hoon Kim, Hoon-Chul Kang, Andreas Schulze-Bonhage, Carola A Haas, Horst Urbach, Marco Prinz, David D Limbrick, Christina A Gurnett, Matthew D Smyth, Shifteh Sattar, Mark Nespeca, David D Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin-Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Wilson Araújo da Silva Junior, Helio R Machado, Gary W Mathern, Alexej Abyzov, Sara Baldassari, Stéphanie Baulac, null null, null null, Joseph G Gleeson
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nature genetics 55 (2) (2023)
Changuk Chung, Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels, H Westley Phillips, Zhen Li, Ashley P L Marsh, Martin W Breuss, Laurel L Ball, Camila Araújo Bernardino Garcia, Renee D George, Jing Gu, Mingchu Xu, Chelsea Barrows, Kiely N James, Valentina Stanley, Anna S Nidhiry, Sami Khoury, Gabrielle Howe, Emily Riley, Xin Xu, Brett Copeland, Yifan Wang, Se-Hoon Kim, Hoon-Chul Kang, Andreas Schulze-Bonhage, Carola A Haas, Horst Urbach, Marco Prinz, David D Limbrick, Christina A Gurnett, Matthew D Smyth, Shifteh Sattar, Mark Nespeca, David D Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin-Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Wilson Araújo da Silva Junior, Helio R Machado, Gary W Mathern, Alexej Abyzov, Sara Baldassari, Stéphanie Baulac, null null, null null, Joseph G Gleeson
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nature genetics 55 (2) (2023)
Changuk Chung, Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels, H Westley Phillips, Zhen Li, Ashley P L Marsh, Martin W Breuss, Laurel L Ball, Camila Araújo Bernardino Garcia, Renee D George, Jing Gu, Mingchu Xu, Chelsea Barrows, Kiely N James, Valentina Stanley, Anna S Nidhiry, Sami Khoury, Gabrielle Howe, Emily Riley, Xin Xu, Brett Copeland, Yifan Wang, Se-Hoon Kim, Hoon-Chul Kang, Andreas Schulze-Bonhage, Carola A Haas, Horst Urbach, Marco Prinz, David D Limbrick, Christina A Gurnett, Matthew D Smyth, Shifteh Sattar, Mark Nespeca, David D Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin-Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Wilson Araújo da Silva Junior, Helio R Machado, Gary W Mathern, Alexej Abyzov, Sara Baldassari, Stéphanie Baulac, null null, null null, Joseph G Gleeson
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nature genetics (2023)
Xiaoxu Yang, Xin Xu, Martin W Breuss, Danny Antaki, Laurel L Ball, Changuk Chung, Jiawei Shen, Chen Li, Renee D George, Yifan Wang, Taejeong Bae, Yuhe Cheng, Alexej Abyzov, Liping Wei, Ludmil B Alexandrov, Jonathan L Sebat, null null, Joseph G Gleeson
Control-independent mosaic single nucleotide variant detection with DeepMosaic. Nature biotechnology (2023)
Changuk Chung, Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels, H Westley Phillips, Zhen Li, Ashley P L Marsh, Martin W Breuss, Laurel L Ball, Camila Araújo Bernardino Garcia, Renee D George, Jing Gu, Mingchu Xu, Chelsea Barrows, Kiely N James, Valentina Stanley, Anna S Nidhiry, Sami Khoury, Gabrielle Howe, Emily Riley, Xin Xu, Brett Copeland, Yifan Wang, Se-Hoon Kim, Hoon-Chul Kang, Andreas Schulze-Bonhage, Carola A Haas, Horst Urbach, Marco Prinz, David D Limbrick, Christina A Gurnett, Matthew D Smyth, Shifteh Sattar, Mark Nespeca, David D Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin-Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Wilson Araújo da Silva Junior, Helio R Machado, Gary W Mathern, Alexej Abyzov, Sara Baldassari, Stéphanie Baulac, null null, null null, Joseph G Gleeson
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nature genetics 55 (2) (2023)
Changuk Chung, Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels, H Westley Phillips, Zhen Li, Ashley P L Marsh, Martin W Breuss, Laurel L Ball, Camila Araújo Bernardino Garcia, Renee D George, Jing Gu, Mingchu Xu, Chelsea Barrows, Kiely N James, Valentina Stanley, Anna S Nidhiry, Sami Khoury, Gabrielle Howe, Emily Riley, Xin Xu, Brett Copeland, Yifan Wang, Se-Hoon Kim, Hoon-Chul Kang, Andreas Schulze-Bonhage, Carola A Haas, Horst Urbach, Marco Prinz, David D Limbrick, Christina A Gurnett, Matthew D Smyth, Shifteh Sattar, Mark Nespeca, David D Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin-Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Wilson Araújo da Silva Junior, Helio R Machado, Gary W Mathern, Alexej Abyzov, Sara Baldassari, Stéphanie Baulac, null null, null null, Joseph G Gleeson
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nature genetics (2023)
Changuk Chung, Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels, H Westley Phillips, Zhen Li, Ashley P L Marsh, Martin W Breuss, Laurel L Ball, Camila Araújo Bernardino Garcia, Renee D George, Jing Gu, Mingchu Xu, Chelsea Barrows, Kiely N James, Valentina Stanley, Anna S Nidhiry, Sami Khoury, Gabrielle Howe, Emily Riley, Xin Xu, Brett Copeland, Yifan Wang, Se-Hoon Kim, Hoon-Chul Kang, Andreas Schulze-Bonhage, Carola A Haas, Horst Urbach, Marco Prinz, David D Limbrick, Christina A Gurnett, Matthew D Smyth, Shifteh Sattar, Mark Nespeca, David D Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin-Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Wilson Araújo da Silva Junior, Helio R Machado, Gary W Mathern, Alexej Abyzov, Sara Baldassari, Stéphanie Baulac, null null, null null, Joseph G Gleeson
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nature genetics 55 (2) (2023)
Changuk Chung, Xiaoxu Yang, Joseph G Gleeson
Post-zygotic brain mosaicism as a result of partial reversion of pre-zygotic aneuploidy. Nature genetics (2023)
Camille Engel, Stéphanie Valence, Geoffroy Delplancq, Reza Maroofian, Andrea Accogli, Emanuele Agolini, Fowzan Sami Alkuraya, Valentina Baglioni, Irene Bagnasco, Mathilde Becmeur-Lefebvre, Enrico Silvio Bertini, Ingo Borggraefe, Elise Brischoux-Boucher, Ange-Line Bruel, Alfredo Brusco, Dalal K Bubshait, Christelle Cabrol, Maria Roberta Cilio, Marie-Coralie Cornet, Christine Coubes, Olivier Danhaive, Valérie Delague, Anne Sophie Denommé-Pichon, Marilena Carmela Di Giacomo, Martine Doco-Fenzy, Hartmut Engels, Kirsten Cremer, Marion Gérard, Joseph G Gleeson, Delphine Heron, Joanna Goffeney, Anne Guimier, Frederike L Harms, Henry Houlden, Michele Iacomino, Rauan Kaiyrzhanov, Benjamin Kamien, Ehsan Ghayoor Karimiani, Dror Kraus, Paul Kuentz, Kerstin Kutsche, Damien Lederer, Lauren Massingham, Cyril Mignot, Deborah J Morris-Rosendahl, Lakshmi Nagarajan, Sylvie Odent, Clothilde Ormières, Jennifer Neil Partlow, Laurent Pasquier, Lynette Penney, Christophe Philippe, Gianluca Piccolo, Cathryn Poulton, Audrey Putoux, Marlène Rio, Christelle Rougeot, Vincenzo Salpietro, Ingrid Scheffer, Amy L Schneider, Siddharth Srivastava, Rachel Straussberg, Pasquale Striano, Enza Maria Valente, Perrine Venot, Laurent Villard, Antonio Vitobello, Johanna Wagner, Matias Wagner, Maha Saad Zaki, Federizo Zara, Gaëtan Lesca, Vahid Reza Yassaee, Mohammad Miryounesi, Feyzollah Hashemi-Gorji, Mehran Beiraghi, Farah Ashrafzadeh, Hamid Galehdari, Christopher A Walsh, Antonio Novelli, Moritz Tacke, Dinara Sadykova, Yerdan Maidyrov, Kairgali Koneev, Chingiz Shashkin, Valeria Capra, Mina Zamani, Lionel Van Maldergem, Lydie Burglen, Juliette Piard
BRAT1-related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patients. European journal of human genetics : EJHG (2023)
Changuk Chung, Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels, H Westley Phillips, Zhen Li, Ashley P L Marsh, Martin W Breuss, Laurel L Ball, Camila Araújo Bernardino Garcia, Renee D George, Jing Gu, Mingchu Xu, Chelsea Barrows, Kiely N James, Valentina Stanley, Anna S Nidhiry, Sami Khoury, Gabrielle Howe, Emily Riley, Xin Xu, Brett Copeland, Yifan Wang, Se-Hoon Kim, Hoon-Chul Kang, Andreas Schulze-Bonhage, Carola A Haas, Horst Urbach, Marco Prinz, David D Limbrick, Christina A Gurnett, Matthew D Smyth, Shifteh Sattar, Mark Nespeca, David D Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin-Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Wilson Araújo da Silva Junior, Helio R Machado, Gary W Mathern, Alexej Abyzov, Sara Baldassari, Stéphanie Baulac, null null, null null, Joseph G Gleeson
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nature genetics 55 (2) (2023)
Changuk Chung, Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels, H Westley Phillips, Zhen Li, Ashley P L Marsh, Martin W Breuss, Laurel L Ball, Camila Araújo Bernardino Garcia, Renee D George, Jing Gu, Mingchu Xu, Chelsea Barrows, Kiely N James, Valentina Stanley, Anna S Nidhiry, Sami Khoury, Gabrielle Howe, Emily Riley, Xin Xu, Brett Copeland, Yifan Wang, Se-Hoon Kim, Hoon-Chul Kang, Andreas Schulze-Bonhage, Carola A Haas, Horst Urbach, Marco Prinz, David D Limbrick, Christina A Gurnett, Matthew D Smyth, Shifteh Sattar, Mark Nespeca, David D Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin-Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Wilson Araújo da Silva Junior, Helio R Machado, Gary W Mathern, Alexej Abyzov, Sara Baldassari, Stéphanie Baulac, null null, null null, Joseph G Gleeson
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nature genetics (2023)
Changuk Chung, Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels, H Westley Phillips, Zhen Li, Ashley P L Marsh, Martin W Breuss, Laurel L Ball, Camila Araújo Bernardino Garcia, Renee D George, Jing Gu, Mingchu Xu, Chelsea Barrows, Kiely N James, Valentina Stanley, Anna S Nidhiry, Sami Khoury, Gabrielle Howe, Emily Riley, Xin Xu, Brett Copeland, Yifan Wang, Se-Hoon Kim, Hoon-Chul Kang, Andreas Schulze-Bonhage, Carola A Haas, Horst Urbach, Marco Prinz, David D Limbrick, Christina A Gurnett, Matthew D Smyth, Shifteh Sattar, Mark Nespeca, David D Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin-Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Wilson Araújo da Silva Junior, Helio R Machado, Gary W Mathern, Alexej Abyzov, Sara Baldassari, Stéphanie Baulac, null null, null null, Joseph G Gleeson
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nature genetics 55 (2) (2023)
Changuk Chung, Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels, H Westley Phillips, Zhen Li, Ashley P L Marsh, Martin W Breuss, Laurel L Ball, Camila Araújo Bernardino Garcia, Renee D George, Jing Gu, Mingchu Xu, Chelsea Barrows, Kiely N James, Valentina Stanley, Anna S Nidhiry, Sami Khoury, Gabrielle Howe, Emily Riley, Xin Xu, Brett Copeland, Yifan Wang, Se-Hoon Kim, Hoon-Chul Kang, Andreas Schulze-Bonhage, Carola A Haas, Horst Urbach, Marco Prinz, David D Limbrick, Christina A Gurnett, Matthew D Smyth, Shifteh Sattar, Mark Nespeca, David D Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin-Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Wilson Araújo da Silva Junior, Helio R Machado, Gary W Mathern, Alexej Abyzov, Sara Baldassari, Stéphanie Baulac, null null, null null, Joseph G Gleeson
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nature genetics 55 (2) (2023)
Ahmet Okay Çağlayan, Beyhan Tuysuz, Ece Gül, Dilek Uludag Alkaya, Cengiz Yalcinkaya, Joseph G Gleeson, Kaya Bilguvar, Murat Günel
Biallelic BICD2 variant is a novel candidate for Cohen-like syndrome. Journal of human genetics 67 (9) (2022)
Danny Antaki, James Guevara, Adam X Maihofer, Marieke Klein, Madhusudan Gujral, Jakob Grove, Caitlin E Carey, Oanh Hong, María Jesús Arranz, Amaia Hervas, Christina Corsello, Keith K Vaux, Alysson Renato Muotri, Lilia M Iakoucheva, Eric Courchesne, Karen Pierce, Joseph G Gleeson, Elise B Robinson, Caroline M Nievergelt, Jonathan Sebat
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex. Nature genetics 54 (9) (2022)
Martin W Breuss, Xiaoxu Yang, Johannes C M Schlachetzki, Danny Antaki, Addison J Lana, Xin Xu, Changuk Chung, Guoliang Chai, Valentina Stanley, Qiong Song, Traci F Newmeyer, An Nguyen, Sydney O'Brien, Marten A Hoeksema, Beibei Cao, Alexi Nott, Jennifer McEvoy-Venneri, Martina P Pasillas, Scott T Barton, Brett R Copeland, Shareef Nahas, Lucitia Van Der Kraan, Yan Ding, null null, Christopher K Glass, Joseph G Gleeson
Somatic mosaicism reveals clonal distributions of neocortical development. Nature 604 (7907) (2022)
Maha Saad Zaki, Andrea Accogli, Ghayda M Mirzaa, Fatima Rahman, Hiba Mohammed, Gloria Liliana Porras-Hurtado, Stephanie Efthymiou, Shazia Maqbool, Anju Shukla, John B Vincent, Abrar Hussain, Asif Mir, Christian Beetz, Anika Leubauer, Henry Houlden, Joseph G Gleeson, Reza Maroofian
Pathogenic variants in PIDD1 lead to an autosomal recessive neurodevelopmental disorder with pachygyria and psychiatric features. European journal of human genetics : EJHG 29 (8) (2021)
Shereen G Ghosh, Martin W Breuss, Zinayida Schlachetzki, Guoliang Chai, Danica Ross, Valentina Stanley, F Mujgan Sonmez, Haluk Topaloglu, Maha Saad Zaki, Heba Hosny, Shaimaa Gad, Joseph G Gleeson
Biallelic hypomorphic mutations in HEATR5B, encoding HEAT repeat-containing protein 5B, in a neurological syndrome with pontocerebellar hypoplasia. European journal of human genetics : EJHG 29 (6) (2021)
Shereen G Ghosh, Marcello Scala, Christian Beetz, Guy Helman, Valentina Stanley, Xiaoxu Yang, Martin W Breuss, Neda Mazaheri, Laila Selim, Fatemeh Hadipour, Lynn Pais, Chloe A Stutterd, Vasiliki Karageorgou, Amber Begtrup, Amy Crunk, Jane Juusola, Rebecca Willaert, Leigh A Flore, Kelly Kennelly, Christopher Spencer, Martha Brown, Pamela Trapane, Anna C E Hurst, S Lane Rutledge, Dana H Goodloe, Marie T McDonald, Vandana Shashi, Kelly Schoch, null null, Hoda Tomoum, Raghda Zaitoun, Zahra Hadipour, Hamid Galehdari, Alistair T Pagnamenta, Majid Mojarrad, Alireza Sedaghat, Patrícia Dias, Sofia Quintas, Atiyeh Eslahi, Gholamreza Shariati, Peter Bauer, Cas Simons, Henry Houlden, Mahmoud Y Issa, Maha Saad Zaki, Reza Maroofian, Joseph G Gleeson
A relatively common homozygous TRAPPC4 splicing variant is associated with an early-infantile neurodegenerative syndrome. European journal of human genetics : EJHG 29 (2) (2020)
Ashleigh E Schaffer, Martin W Breuss, Ahmet Okay Caglayan, Nouriya Al-Sanaa, Hind Y Al-Abdulwahed, Hande Kaymakçalan, Cahide Yılmaz, Maha S Zaki, Rasim O Rosti, Brett Copeland, Seung Tae Baek, Damir Musaev, Eric C Scott, Tawfeg Ben-Omran, Ariana Kariminejad, Hulya Kayserili, Faezeh Mojahedi, Majdi Kara, Na Cai, Jennifer L Silhavy, Seham Elsharif, Elif Fenercioglu, Bruce A Barshop, Bulent Kara, Rengang Wang, Valentina Stanley, Kiely N James, Rahul Nachnani, Aneesha Kalur, Hisham Megahed, Faruk Incecik, Sumita Danda, Yasemin Alanay, Eissa Faqeih, Gia Melikishvili, Lobna Mansour, Ian Miller, Biayna Sukhudyan, Jamel Chelly, William B Dobyns, Kaya Bilguvar, Rami Abou Jamra, Murat Gunel, Joseph G Gleeson
Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration. Nature genetics 50 (8) (2018)

Joseph G Gleeson.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

Joseph G Gleeson