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Ian A. Glass

university of washington

61H-index
294Paper Count
2.2WCitation Count
Published Papers 103
Publication Date
Mapping mesenchymal diversity in the human small intestine and organoids
err2026-07-22
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errOAAI
errKelli F. Johnson; Xiangning Dong; Yu-Hwai Tsai; Angeline Wu; Sydney G. Clark; Abigail Vallie; Sha Huang; Charlie J. Childs; Rachel K. Zwick; Ian Glass; Katherine D. Walton; Ophir D. Klein; Jason R. Spence
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Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes
err2026-05-18
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errOAAI
errRocio Rius; Alexander J. M. Blakes; Yuyang Chen; Joachim De Jonghe; François Lecoquierre; Ruebena Dawes; Benjamin Cogne; Hyung Chul Kim; Javeria R. Alvi; Florence Amblard; Morad Ansari; Annabelle Arlt; Christina Austin-Tse; Sarah Baer; Meena Balasubramanian; Elsa V. Balton; Giulia Barcia; Ana Beleza-Meireles; Jonathan A. Bernstein; Jasmin Beygo; Pierre Blanc; Nuria C. Bramswig; Frederik Braun; Daniel Buchzik; Daniel G. Calame; Jamie Campbell; Charles Coutton; Chloe A. Cunningham; Nitsuh Dargie; Christel Depienne; Katrina M. Dipple; Anne Dieux; Abhijit Dixit; Lauren Dreyer; Haowei Du; Salima El Chehadeh; Michael Field; Lisa J. Ewans; Vanessa Geiger; Richard A. Gibbs; Ian Glass; Olivier Grunewald; Paul Gueguen; Tobias B. Haack; Hamza Hadj Abdallah; Radu Harbuz; Ingo Helbig; Judit Horvath; Alexander Hustinx; Bertrand Isidor; Marie-Line Jacquemont; Fraser Jamie; Médéric Jeanne; Riley Kessler; Hannah Klinkhammer; G. Christoph Korenke; Urania Kotzaeridou; Peter Krawitz; Steven Laurie; Richard J. Leventer; Rebecca J. Levy; James R. Lupski; Pierre Marijon; Kaitlin E. McGinnis; Rodrigo Mendez; Olfa Messaoud; Caroline Nava; Mevyn Nizard; Anne O’Donnell-Luria; Melanie C. O’Leary; Simone Olivieri; Amitav Parida; Davut Pehlivan; Anna Jenne Prentice; Jennifer E. Posey; Chloe M. Reuter; Véronique Satre; Caroline Schluth-Bolard; Thomas Smol; Tipu Sultan; John Taylor; Christel Thauvin-Robinet; Julien Thevenon; Eloise Uebergang; Sandra Ueberberg; Catherine Vincent-Delorme; Evangeline Wassmer; Emma Westwood; Matthew T. Wheeler; Elif Yilmaz Gulec; Adeline Vanderver; Arastoo Vossough; Stephan J. Sanders; Siddharth Banka; Gregory M. Findlay; Daniel G. MacArthur; Cas Simons; Nicola Whiffin
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Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes
err2026-04-08
err0
errOAAI
errRocio Rius; Alexander J. M. Blakes; Yuyang Chen; Joachim De Jonghe; François Lecoquierre; Ruebena Dawes; Benjamin Cogne; Hyung Chul Kim; Javeria R. Alvi; Florence Amblard; Morad Ansari; Annabelle Arlt; Christina Austin-Tse; Sarah Baer; Meena Balasubramanian; Elsa V. Balton; Giulia Barcia; Ana Beleza-Meireles; Jonathan A. Bernstein; Jasmin Beygo; Pierre Blanc; Nuria C. Bramswig; Frederik Braun; Daniel Buchzik; Daniel G. Calame; Jamie Campbell; Charles Coutton; Chloe A. Cunningham; Nitsuh Dargie; Christel Depienne; Katrina M. Dipple; Anne Dieux; Abhijit Dixit; Lauren Dreyer; Haowei Du; Salima El Chehadeh; Michael Field; Lisa J. Ewans; Vanessa Geiger; Richard A. Gibbs; Ian Glass; Olivier Grunewald; Paul Gueguen; Tobias B. Haack; Hamza Hadj Abdallah; Radu Harbuz; Ingo Helbig; Judit Horvath; Alexander Hustinx; Bertrand Isidor; Marie-Line Jacquemont; Fraser Jamie; Médéric Jeanne; Riley Kessler; Hannah Klinkhammer; G. Christoph Korenke; Urania Kotzaeridou; Peter Krawitz; Steven Laurie; Richard J. Leventer; Rebecca J. Levy; James R. Lupski; Pierre Marijon; Kaitlin E. McGinnis; Rodrigo Mendez; Olfa Messaoud; Caroline Nava; Mevyn Nizard; Anne O’Donnell-Luria; Melanie C. O’Leary; Simone Olivieri; Amitav Parida; Davut Pehlivan; Anna Jenne Prentice; Jennifer E. Posey; Chloe M. Reuter; Véronique Satre; Caroline Schluth-Bolard; Thomas Smol; Tipu Sultan; John Taylor; Christel Thauvin-Robinetvin; Julien Thevenon; Eloise Uebergang; Sandra Ueberberg; Catherine Vincent-Delorme; Evangeline Wassmer; Emma Westwood; Matthew T. Wheeler; Elif Yilmaz Gulec; Adeline Vanderver; Arastoo Vossough; Stephan J. Sanders; Siddharth Banka; Gregory M. Findlay; Daniel G. MacArthur; Cas Simons; Nicola Whiffin
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Saturation editing of RNU4-2 reveals distinct dominant and recessive disorders
errNature
IF48.5
err2026-04-08
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errOAAI
errJoachim De Jonghe; Hyung Chul Kim; Ayanfeoluwa Adedeji; Elsa Leitão; Ruebena Dawes; Christina M. Kajba; Benjamin Cogné; Yuyang Chen; Alexander J. M. Blakes; Cas Simons; Rocio Rius; Javeria R. Alvi; Florence Amblard; Christina Austin-Tse; Sarah Baer; Elsa V. Balton; Pierre Blanc; Daniel G. Calame; Charles Coutton; Chloe A. Cunningham; Nitsuh Dargie; Katrina M. Dipple; Haowei Du; Salima El Chehadeh; Ian Glass; Joseph G. Gleeson; Olivier Grunewald; Paul Gueguen; Radu Harbuz; Marie-Line Jacquemont; Richard J. Leventer; Pierre Marijon; Olfa Messaoud; Tipu Sultan; Christel Thauvin; Catherine Vincent-Delorme; Elif Yilmaz Gulec; Julien Thevenon; Rodrigo Mendez; Daniel G. MacArthur; Christel Depienne; Caroline Nava; Nicola Whiffin; Gregory M. Findlay
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Rete ridges form via evolutionarily distinct mechanisms in mammalian skin
errNature
IF48.5
err2026-02-04
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errOAAI
errSean M. Thompson; Violet S. Yaple; Gabriella H. Searle; Quan M. Phan; Jasson Makkar; Xiangzheng Cheng; Ruiqi Liu; Anna Pulawska-Czub; Corin Yanke; Natalie M. Williams; Isabelle V. Busch; Tommy T. Duong; Matteo V. Corneto; Zachary S. Jordan; Debarun Roy; Adam B. Salmon; Ov D. Slayden; Brian P. Hermann; David A. Stoltz; Michael J. Welsh; Ian A. Glass; Krzysztof Kobielak; Qing Nie; Suoqin Jin; Heiko T. Jansen; Michela Ciccarelli; Maksim V. Plikus; Iwona M. Driskell; Ryan R. Driskell
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De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disorders
err2026-01-23
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errOAAI
errKevin Uguen; Tiffany Bergot; Marie-Pier Scott-Boyer; Solène Chapalain; Camille Desdouets; Séverine Commet; Changlian Zhu; Yiran Xu; Yangong Wang; Tony Roscioli; Frederic Tran-Mau-Them; Laurence Faivre; Julien Maraval; Julian Delanne; Anne-Sophie Denommé-Pichon; Antonio Vitobello; Céline Jost; Marc Planes; Susan Hiatt; Patricia Wheeler; Claudia Gonzaga-Jauregui; Heng Wang; Baozhong Xin; Valerie Sency; Michael C. Kruer; Somayeh Bakhtiari; Patrick Sulem; Cynthia Curry; Trine Prescott; Gertrud Strobl-Wildemann; Theresa Brunet; Martine Doco Fenzy; Thomas Courtin; Céline Poirsier; Trine Bjørg Hammer; Christina D. Fenger; Melissa MacPherson; Kosuke Izumi; Jacqueline Leonard; Dong Li; Elaine H. Zackai; Ian A. Glass; Scott Ward; Philippe M. Campeau; Maria Carla Hermida Borroto; Laurence Le Moigno; Hilde Van Esch; Liesbeth De Waele; Daniel G. Calame; James R. Lupski; Giulia Barcia; Cristina Peduto; Pauline Planté-Bordeneuve; Lucie Dupuis; Roberto Mendoza-Londono; Dimitri J. Stavropoulos; Jennifer Gillibert-Duplantier; Thomas Besnard; Laura Do Souto Ferreira; Benjamin Cogné; Stéphane Bézieau; Arnaud Droit; Laurent Corcos; Eric Lippert; Claude Férec; Sebastien Küry; Delphine G. Bernard
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DIO3 coordinates photoreceptor development timing and fate stability in human retinal organoids
err2026-01-01
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PREAI
errMcnerney, Christina; Santiago, Clayton P.; Eldred, Kiara C.; Glass, Ian; Reh, Tom A.; Hernandez, Arturo; Blackshaw, Seth; Lord, Nathan D.; Johnston Jr, Robert J.
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Alterations in Resident Immune Cells in Prenatal Trisomy 21 Lungs
err2025-11-26
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errOAAI
errAndrew Frauenpreis; Soumyaroop Bhattacharya; Randa Belgacemi; Pauline Sokolskiy; Gail Deutsch; Nicholas Jendzjowsky; Ian A. Glass; Thomas J. Mariani; Denise Al Alam; Soula Danopoulos
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Missense variants in DPYSL5 associated with neurodevelopmental disorders and brain malformations cause impaired neuronal maturation in vitro
err2025-11-24
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errOAAI
errFlorence Desprez; Solène Remize; Liberty François-Moutal; Dévina C. Ung; Audrey Dangoumau; Sylviane Marouillat; Joanna Kennedy; Karen J. Low; Camille Kumps; Sheila Unger; Boris Keren; Jean-Madeleine de Sainte Agathe; Céline Poirsier; Ghayda M. Mirzaa; Kimberly A. Aldinger; Gaetan Lesca; Valentin Ruault; Candice R. Finnila; Whitley V. Kelley; Donald R. Latner; Sushma N. Guptha; Annabelle Tuttle; Ian Glass; Wendy K. Chung; Jennifer Cassady Hayek; Odile Boute; Aubin Moutal; Médéric Jeanne; Frédéric Laumonnier
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Case Report: An atypical case of ARPKD highlights the utility and challenges of implementing genetic testing in cystic kidney disease
err2025-11-03
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errOAAI
errMarquez, Jonathan; Hawkins, Lauren M.; Beck, Anita E.; Dipple, Katrina M.; Glass, Ian A.; Keefe, Alexandra C.; Nguyen, Elizabeth D.
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The mGluR5 agonist CHPG enhances human oligodendrocyte differentiation
err2025-10-04
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errOAAI
errYangyang Huang; Celine Geywitz; Anjalika Bandaru; Ian A Glass; Lucas Schirmer; Hiroko Nobuta; Cheryl F Dreyfus
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The evolution of hominin bipedalism in two steps
errNature
IF48.5
err2025-08-27
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errOAAI
errGayani Senevirathne; Serena C. Fernandopulle; Daniel Richard; Stephanie L. Baumgart; Anika Liv Christensen; Matteo Fabbri; Jakob Höppner; Harald Jüppner; Peishu Li; Vivien Bothe; Nadia Fröbisch; Ian Simcock; Owen J. Arthurs; Alistair Calder; Naomi Freilich; Niamh C. Nowlan; Ian A. Glass; April Craft; Terence D. Capellini
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The human neural cell atlas of Zika virus infection in developing brain tissue
err2025-06-17
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errOAAI
errCaleb Stokes; Leanne S. Whitmore; Dante Moreno; Karan Malhotra; Jennifer Tisoncik-Go; Emily Tran; Nick Wren; Ian A. Glass; Jessica E. Young; Michael Gale
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Chromosomal instability in human trophoblast stem cells and placentas
err2025-04-25
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errOAAI
errWang, Danyang; Cearlock, Andrew; Lane, Katherine; Xu, Chongchong; Jan, Ian; McCartney, Stephen; Glass, Ian; McCoy, Rajiv
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Ciliary marginal zone of the developing human retina maintains retinal progenitor cells until late gestational stages
err2025-04-01
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errOAAI
errEldred, Kiara C.; Edgerton, Sierra J.; Ortuno-Lizaran, Isabel; Wohlschlegel, Juliette; Sherman, Stephanie M.; Petter, Sidnee; Wyatt-Draher, Gracious; Hoffer, Dawn; Glass, Ian; Reh, Thomas A.
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Developmental control of rod number via a light-dependent retrograde pathway from intrinsically photosensitive retinal ganglion cells
err2024-11-01
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PREAI
errD'Souza, Shane P.; Upton, Brian A.; Eldred, Kiara C.; Glass, Ian; Nayak, Gowri; Grover, Kassidy; Ahmed, Abdulla; Nguyen, Minh-Thanh; Hu, Yueh-Chiang; Gamlin, Paul; Lang, Richard A.
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APOE-NOTCH axis governs elastogenesis during human cardiac valve remodeling
err2024-07-24
err3
PREAI
errLiu, Ziyi; Liu, Yu; Yu, Zhiyun; Tan, Cheng; Pek, Nicole; O'Donnell, Anna; Wu, Angeline; Glass, Ian; Winlaw, David S.; Guo, Minzhe; Spence, Jason R.; Chen, Ya-Wen; Yutzey, Katherine E.; Miao, Yifei; Gu, Mingxia
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De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (vol 111, pg 778, 2024)
err2024-06-01
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errOAAI
errMullegama, Sureni V.; Kiernan, Kaitlyn A.; Torti, Erin; Pavlovsky, Ethan; Tilton, Nicholas; Sekula, Austin; Gao, Hua; Alaimo, Joseph T.; Engleman, Kendra; Rush, Eric T.; Blocker, Karli; Dipple, Katrina M.; Fettig, Veronica M.; Hare, Heather; Glass, Ian; Grange, Dorothy K.; Griffin, Michael; Phornphutkul, Chanika; Massingham, Lauren; Mehta, Lakshmi; Miller, Danny E.; Thies, Jenny; Merritt, J. Lawrence; Muller, Eric; Osmond, Matthew; Sawyer, Sarah L.; Slaugh, Rachel; Hickey, Rachel E.; Wolf, Barry; Choudhary, Sanjeev; Simonovic, Miljan; Zhang, Yueqing; Palculict, Timothy Blake; Telegrafi, Aida; Carere, Deanna Alexis; Wentzensen, Ingrid M.; Morrow, Michelle M.; Monaghan, Kristin G.; Juusola, Jane; Yang, Jun
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De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features
err2024-04-01
err2
errOAAI
errMullegama, Sureni V.; Kiernan, Kaitlyn A.; Torti, Erin; Pavlovsky, Ethan; Tilton, Nicholas; Sekula, Austin; Gao, Hua; Alaimo, Joseph T.; Engleman, Kendra; Rush, Eric T.; Blocker, Karli; Dipple, Katrina M.; Fettig, Veronica M.; Hare, Heather; Glass, Ian; Grange, Dorothy K.; Griffin, Michael; Phornphutkul, Chanika; Massingham, Lauren; Mehta, Lakshmi; Miller, Danny E.; Thies, Jenny; Merritt II, J. Lawrence; Muller II, Eric; Osmond, Matthew; Sawyer, Sarah L.; Slaugh, Rachel; Hickey, Rachel E.; Wolf, Barry; Choudhary, Sanjeev; Simonovic, Miljan; Zhang, Yueqing; Palculict, Timothy Blake; Telegrafi, Aida; Carere, Deanna Alexis; Wentzensen, Ingrid M.; Morrow, Michelle M.; Monaghan, Kristin G.; Yang, Jun; Juusola, Jane
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Sweat gland development requires an eccrine dermal niche and couples two epidermal programs
err2024-01-01
err3
errOAAI
errDingwall, Heather L.; Tomizawa, Reiko R.; Aharoni, Adam; Hu, Peng; Qiu, Qi; Kokalari, Blerina; Martinez, Serenity M.; Donahue, Joan C.; Aldea, Daniel; Mendoza, Meryl; Glass, Ian A.; Wu, Hao; Kamberov, Yana G.
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