Sarah Vergult

ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 19

Top Venues

Nature communications

Genome biology

Nature genetics

medRxiv : the preprint server for health sciences

Ghent University

Ghent University (MSC)

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

Affiliation History

Ghent University Oct 01 2019

Belgium

Assistant professor :: GE31 - Department of Biomolecular Medicine

Ghent University Oct 01 2016 - Sep 30 2019

Belgium

FWO Postdoctoral fellow :: GE31 BioMolecular Medicine

Ghent University Oct 01 2013 - Sep 30 2016

Belgium

BOF Postdoctoral fellow :: GE02 - Department of Pediatrics and Genetics

Ghent University Oct 01 2012 - Sep 30 2013

Belgium

Scientific Collaborator :: GE02

Ghent University Oct 01 2008 - Sep 30 2012

Belgium

FWO PhD fellow :: GE02

Education History

Ghent University Oct 01 2003 - Jul 05 2008

Belgium

MSC :: Faculty of Bio-engineering

Publications

Andrea Wilderman, Eva D'haene, Machteld Baetens, Tara N Yankee, Emma Wentworth Winchester, Nicole Glidden, Ellen Roets, Jo Van Dorpe, Sandra Janssens, Danny E Miller, Miranda Perez-Galey Zalusky, Kari M Brown, Rolf W Stottmann, Sarah Vergult, K Nicole Weaver, Samantha A Brugmann, Timothy C Cox, Justin L Cotney
A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development. Nature communications 15 (1) (2024)
Andrea Wilderman, Eva D'haene, Machteld Baetens, Tara N Yankee, Emma Wentworth Winchester, Nicole Glidden, Ellen Roets, Jo Van Dorpe, Sandra Janssens, Danny E Miller, Miranda Perez-Galey Zalusky, Kari M Brown, Rolf W Stottmann, Sarah Vergult, K Nicole Weaver, Samantha A Brugmann, Timothy C Cox, Justin L Cotney
A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development. Nature communications 15 (1) (2024)
Eva D'haene, Víctor López-Soriano, Pedro Manuel Martínez-García, Soraya Kalayanamontri, Alfredo Dueñas Rey, Ana Sousa-Ortega, Silvia Naranjo, Stijn Van de Sompele, Lies Vantomme, Quinten Mahieu, Sarah Vergult, Ana Neto, José Luis Gómez-Skarmeta, Juan Ramón Martinez-Morales, Miriam Bauwens, Juan Jesús Tena, Elfriede De Baere
Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci. Genome biology 25 (1) (2024)
Eva D'haene, Víctor López-Soriano, Pedro Manuel Martínez-García, Soraya Kalayanamontri, Alfredo Dueñas Rey, Ana Sousa-Ortega, Silvia Naranjo, Stijn Van de Sompele, Lies Vantomme, Quinten Mahieu, Sarah Vergult, Ana Neto, José Luis Gómez-Skarmeta, Juan Ramón Martinez-Morales, Miriam Bauwens, Juan Jesús Tena, Elfriede De Baere
Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci. Genome biology 25 (1) (2024)
María Del Rocío Pérez Baca, Maria Palomares-Bralo, Michiel Vanhooydonck, Lisa Hamerlinck, Eva D'haene, Sebastian Leimbacher, Eva Z Jacobs, Laurenz De Cock, Erika D'haenens, Annelies Dheedene, Zoë Malfait, Lies Vantomme, Ananilia Silva, Kathleen Rooney, Fernando Santos-Simarro, Roser Lleuger-Pujol, Sixto García-Miñaúr, Itsaso Losantos-García, Björn Menten, Gaia Gestri, Nicola Ragge, null null, Bekim Sadikovic, Elke Bogaert, Delfien Syx, Bert Callewaert, Sarah Vergult
Loss-of-function of the Zinc Finger Homeobox 4 ( ZFHX4 ) gene underlies a neurodevelopmental disorder. medRxiv : the preprint server for health sciences (2024)
María Del Rocío Pérez Baca, Maria Palomares-Bralo, Michiel Vanhooydonck, Lisa Hamerlinck, Eva D'haene, Sebastian Leimbacher, Eva Z Jacobs, Laurenz De Cock, Erika D'haenens, Annelies Dheedene, Zoë Malfait, Lies Vantomme, Ananilia Silva, Kathleen Rooney, Fernando Santos-Simarro, Roser Lleuger-Pujol, Sixto García-Miñaúr, Itsaso Losantos-García, Björn Menten, Gaia Gestri, Nicola Ragge, null null, Bekim Sadikovic, Elke Bogaert, Delfien Syx, Bert Callewaert, Sarah Vergult
Loss-of-function of the Zinc Finger Homeobox 4 ( ZFHX4 ) gene underlies a neurodevelopmental disorder. medRxiv : the preprint server for health sciences (2024)
Andrea Wilderman, Eva D'haene, Machteld Baetens, Tara N Yankee, Emma Wentworth Winchester, Nicole Glidden, Ellen Roets, Jo Van Dorpe, Sandra Janssens, Danny E Miller, Miranda Perez-Galey Zalusky, Kari M Brown, Rolf W Stottmann, Sarah Vergult, K Nicole Weaver, Samantha A Brugmann, Timothy C Cox, Justin L Cotney
A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development. Nature communications 15 (1) (2024)
Andrea Wilderman, Eva D'haene, Machteld Baetens, Tara N Yankee, Emma Wentworth Winchester, Nicole Glidden, Ellen Roets, Jo Van Dorpe, Sandra Janssens, Danny E Miller, Miranda Perez-Galey Zalusky, Kari M Brown, Rolf W Stottmann, Sarah Vergult, K Nicole Weaver, Samantha A Brugmann, Timothy C Cox, Justin L Cotney
A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development. Nature communications 15 (1) (2024)
Eva D'haene, Víctor López-Soriano, Pedro Manuel Martínez-García, Soraya Kalayanamontri, Alfredo Dueñas Rey, Ana Sousa-Ortega, Silvia Naranjo, Stijn Van de Sompele, Lies Vantomme, Quinten Mahieu, Sarah Vergult, Ana Neto, José Luis Gómez-Skarmeta, Juan Ramón Martinez-Morales, Miriam Bauwens, Juan Jesús Tena, Elfriede De Baere
Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci. Genome biology 25 (1) (2024)
Andrea Wilderman, Eva D'haene, Machteld Baetens, Tara N Yankee, Emma Wentworth Winchester, Nicole Glidden, Ellen Roets, Jo Van Dorpe, Sandra Janssens, Danny E Miller, Miranda Perez-Galey Zalusky, Kari M Brown, Rolf W Stottmann, Sarah Vergult, K Nicole Weaver, Samantha A Brugmann, Timothy C Cox, Justin L Cotney
A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development. Nature communications 15 (1) (2024)
Andrea Wilderman, Eva D'haene, Machteld Baetens, Tara N Yankee, Emma Wentworth Winchester, Nicole Glidden, Ellen Roets, Jo Van Dorpe, Sandra Janssens, Danny E Miller, Miranda Perez-Galey Zalusky, Kari M Brown, Rolf W Stottmann, Sarah Vergult, K Nicole Weaver, Samantha A Brugmann, Timothy C Cox, Justin L Cotney
A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development. Nature communications 15 (1) (2024)
María Del Rocío Pérez Baca, Eva Z Jacobs, Lies Vantomme, Pontus Leblanc, Elke Bogaert, Annelies Dheedene, Laurenz De Cock, Sadegheh Haghshenas, Aidin Foroutan, Michael A Levy, Jennifer Kerkhof, Haley McConkey, Chun-An Chen, Nurit Assia Batzir, Xia Wang, Maria Palomares, Marieke Carels, null null, Bart Demaut, Bekim Sadikovic, Björn Menten, Bo Yuan, Sarah Vergult, Bert Callewaert
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene. medRxiv : the preprint server for health sciences (2023)
Ilse Meerschaut, Sarah Vergult, Annelies Dheedene, Björn Menten, Katya De Groote, Hans De Wilde, Laura Muiño Mosquera, Joseph Panzer, Kristof Vandekerckhove, Paul J Coucke, Daniël De Wolf, Bert Callewaert
A Reassessment of Copy Number Variations in Congenital Heart Defects: Picturing the Whole Genome. Genes 12 (7) (2021)
Candy Kumps, Erika D'haenens, Sarah Vergult, Jasmine Leus, Rudy van Coster, Anna Jansen, Koen Devriendt, Anna Oostra, Olivier M Vanakker
Phenotypic spectrum of the RBM10-mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome features. Clinical genetics 99 (3) (2021)
Eva Z Jacobs, Kathleen Brown, Melissa C Byler, Erika D'haenens, Annelies Dheedene, Lindsay B Henderson, Jennifer B Humberson, Richard H van Jaarsveld, Farah Kanani, Robert Roger Lebel, Francisca Millan, Renske Oegema, Ann Oostra, Michael J Parker, Lindsay Rhodes, Margarita Saenz, Laurie H Seaver, Yue Si, Arnaud Vanlander, Sarah Vergult, Bert Callewaert
Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variants. Clinical genetics 99 (2) (2020)
Maria Felicia Basilicata, Ange-Line Bruel, Giuseppe Semplicio, Claudia Isabelle Keller Valsecchi, Tuğçe Aktaş, Yannis Duffourd, Tobias Rumpf, Jenny Morton, Iben Bache, Witold G Szymanski, Christian Gilissen, Olivier Vanakker, Katrin Õunap, Gerhard Mittler, Ineke van der Burgt, Salima El Chehadeh, Megan T Cho, Rolph Pfundt, Tiong Yang Tan, Maria Kirchhoff, Björn Menten, Sarah Vergult, Kristin Lindstrom, André Reis, Diana S Johnson, Alan Fryer, Victoria McKay, null null, Richard B Fisher, Christel Thauvin-Robinet, David Francis, Tony Roscioli, Sander Pajusalu, Kelly Radtke, Jaya Ganesh, Han G Brunner, Meredith Wilson, Laurence Faivre, Vera M Kalscheuer, Julien Thevenon, Asifa Akhtar
De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation. Nature genetics 50 (10) (2018)
Eva Z Jacobs, Sharat Warrier, Pieter-Jan Volders, Eva D'haene, Eva Van Lombergen, Lies Vantomme, Margot Van der Jeught, Björn Heindryckx, Björn Menten, Sarah Vergult
CRISPR/Cas9-mediated genome editing in naïve human embryonic stem cells. Scientific reports 7 (1) (2017)
Daniela A Braun, Jia Rao, Geraldine Mollet, David Schapiro, Marie-Claire Daugeron, Weizhen Tan, Olivier Gribouval, Olivia Boyer, Patrick Revy, Tilman Jobst-Schwan, Johanna Magdalena Schmidt, Jennifer A Lawson, Denny Schanze, Shazia Ashraf, Jeremy F P Ullmann, Charlotte A Hoogstraten, Nathalie Boddaert, Bruno Collinet, Gaëlle Martin, Dominique Liger, Svjetlana Lovric, Monica Furlano, I Chiara Guerrera, Oraly Sanchez-Ferras, Jennifer F Hu, Anne-Claire Boschat, Sylvia Sanquer, Björn Menten, Sarah Vergult, Nina De Rocker, Merlin Airik, Tobias Hermle, Shirlee Shril, Eugen Widmeier, Heon Yung Gee, Won-Il Choi, Carolin E Sadowski, Werner L Pabst, Jillian K Warejko, Ankana Daga, Tamara Basta, Verena Matejas, Karin Scharmann, Sandra D Kienast, Babak Behnam, Brendan Beeson, Amber Begtrup, Malcolm Bruce, Gaik-Siew Ch'ng, Shuan-Pei Lin, Jui-Hsing Chang, Chao-Huei Chen, Megan T Cho, Patrick M Gaffney, Patrick E Gipson, Chyong-Hsin Hsu, Jameela A Kari, Yu-Yuan Ke, Cathy Kiraly-Borri, Wai-Ming Lai, Emmanuelle Lemyre, Rebecca Okashah Littlejohn, Amira Masri, Mastaneh Moghtaderi, Kazuyuki Nakamura, Fatih Ozaltin, Marleen Praet, Chitra Prasad, Agnieszka Prytuła, Elizabeth R Roeder, Patrick Rump, Rhonda E Schnur, Takashi Shiihara, Manish D Sinha, Neveen A Soliman, Kenza Soulami, David A Sweetser, Wen-Hui Tsai, Jeng-Daw Tsai, Rezan Topaloglu, Udo Vester, David H Viskochil, Nithiwat Vatanavicharn, Jessica L Waxler, Klaas J Wierenga, Matthias T F Wolf, Sik-Nin Wong, Sebastian A Leidel, Gessica Truglio, Peter C Dedon, Annapurna Poduri, Shrikant Mane, Richard P Lifton, Maxime Bouchard, Peter Kannu, David Chitayat, Daniella Magen, Bert Callewaert, Herman van Tilbeurgh, Martin Zenker, Corinne Antignac, Friedhelm Hildebrandt
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly. Nature genetics 49 (10) (2017)
Claire Redin, Harrison Brand, Ryan L Collins, Tammy Kammin, Elyse Mitchell, Jennelle C Hodge, Carrie Hanscom, Vamsee Pillalamarri, Catarina M Seabra, Mary-Alice Abbott, Omar A Abdul-Rahman, Erika Aberg, Rhett Adley, Sofia L Alcaraz-Estrada, Fowzan Sami Alkuraya, Yu An, Mary-Anne Anderson, Caroline Antolik, Kwame Anyane-Yeboa, Joan F Atkin, Tina Bartell, Jonathan A Bernstein, Elizabeth Beyer, Ian Blumenthal, Ernie M H F Bongers, Eva H Brilstra, Chester W Brown, Hennie T Brüggenwirth, Bert Callewaert, Colby Chiang, Ken Corning, Helen Cox, Edwin Cuppen, Benjamin B Currall, Tom Cushing, Dezso David, Matthew A Deardorff, Annelies Dheedene, Marc D'Hooghe, Bert B A de Vries, Dawn L Earl, Heather L Ferguson, Heather Fisher, David R FitzPatrick, Pamela Gerrol, Daniela Giachino, Joseph T Glessner, Troy Gliem, Margo Grady, Brett H Graham, Cristin Griffis, Karen W Gripp, Andrea L Gropman, Andrea Hanson-Kahn, David J Harris, Mark A Hayden, Rosamund Hill, Ron Hochstenbach, Jodi D Hoffman, Robert J Hopkin, Monika W Hubshman, A Micheil Innes, Mira Irons, Melita Irving, Jessie C Jacobsen, Sandra Janssens, Tamison Jewett, John P Johnson, Marjolijn C Jongmans, Stephen G Kahler, David A Koolen, Jerome Korzelius, Peter M Kroisel, Yves Lacassie, William Lawless, Emmanuelle Lemyre, Kathleen Leppig, Alex V Levin, Haibo Li, Hong Li, Eric C Liao, Cynthia Lim, Edward J Lose, Diane Lucente, Michael J Macera, Poornima Manavalan, Giorgia Mandrile, Carlo L Marcelis, Lauren Margolin, Tamara Mason, Diane Masser-Frye, Michael W McClellan, Cinthya J Zepeda Mendoza, Björn Menten, Sjors Middelkamp, Liya R Mikami, Emily Moe, Shehla Mohammed, Tarja Mononen, Megan E Mortenson, Graciela Moya, Aggie W Nieuwint, Zehra Ordulu, Sandhya Parkash, Susan P Pauker, Shahrin Pereira, Danielle Perrin, Katy Phelan, Raul E Piña Aguilar, Pino J Poddighe, Giulia Pregno, Salmo Raskin, Linda Reis, William Rhead, Debra Rita, Ivo Renkens, Filip Roelens, Jayla Ruliera, Patrick Rump, Samantha L P Schilit, Ranad Shaheen, Rebecca Sparkes, Erica Spiegel, Blair Stevens, Matthew R Stone, Julia Tagoe, Joseph V Thakuria, Bregje W van Bon, Jiddeke van de Kamp, Ineke van Der Burgt, Ton van Essen, Conny M van Ravenswaaij-Arts, Markus J van Roosmalen, Sarah Vergult, Catharina M L Volker-Touw, Dorothy P Warburton, Matthew J Waterman, Susan Wiley, Anna Wilson, Maria de la Concepcion A Yerena-de Vega, Roberto T Zori, Brynn Levy, Han G Brunner, Nicole de Leeuw, Wigard P Kloosterman, Erik C Thorland, Cynthia C Morton, James F Gusella, Michael E Talkowski
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. Nature genetics 49 (1) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Sarah Vergult