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E

Elise Héon

university of toronto

56H-index
271Paper Count
1.2WCitation Count
Published Papers 92
Publication Date
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Gene therapy outcomes in young patients with RPE65-retinal degeneration
errCanadian Journal of Ophthalmology
IF1.8
err2026-02-27
err0
errOAAI
errKirk A.J. Stephenson; Abrar K. Alsalamah; Anupreet Tumber; Gareth D. Mercer; Brian G. Ballios; Rajeev H. Muni; Erika Tavares; Peter J. Kertes; Ajoy Vincent; Elise Héon
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De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa
errNature Genetics
IF29
err2026-01-09
err0
errOAAI
errMathieu Quinodoz; Kim Rodenburg; Zuzana Cvackova; Karolina Kaminska; Suzanne E. de Bruijn; Ana Belén Iglesias-Romero; Erica G. M. Boonen; Mukhtar Ullah; Nick Zomer; Marc Folcher; Jacques Bijon; Lara K. Holtes; Stephen H. Tsang; Zelia Corradi; K. Bailey Freund; Stefanida Shliaga; Daan M. Panneman; Rebekkah J. Hitti-Malin; Manir Ali; Ala’a AlTalbishi; Sten Andréasson; Georg Ansari; Gavin Arno; Galuh D. N. Astuti; Carmen Ayuso; Radha Ayyagari; Sandro Banfi; Eyal Banin; Tahsin Stefan Barakat; Mirella T. S. Barboni; Miriam Bauwens; Tamar Ben-Yosef; Virginie Bernard; David G. Birch; Pooja Biswas; Fiona Blanco-Kelly; Beatrice Bocquet; Camiel J. F. Boon; Kari Branham; Dominique Bremond-Gignac; Alexis Ceecee Britten-Jones; Kinga M. Bujakowska; Cyril Burin des Roziers; Elizabeth L. Cadena; Giacomo Calzetti; Francesca Cancellieri; Luca Cattaneo; Naomi Chadderton; Peter Charbel Issa; Luísa Coutinho-Santos; Stephen P. Daiger; Elfride De Baere; Marieke De Bruyne; Berta de la Cerda; John N. De Roach; Julie De Zaeytijd; Ronny Derks; Claire-Marie Dhaenens; Lubica Dudakova; Jacque L. Duncan; G. Jane Farrar; Nicolas Feltgen; Beau J. Fenner; Lidia Fernández-Caballero; Juliana M. Ferraz Sallum; Simone Gana; Alejandro Garanto; Jessica C. Gardner; Christian Gilissen; Roser Gonzàlez-Duarte; Kensuke Goto; Sam Griffiths-Jones; Tobias B. Haack; Lonneke Haer-Wigman; Alison J. Hardcastle; Takaaki Hayashi; Elise Héon; Lies H. Hoefsloot; Alexander Hoischen; Josephine P. Holtan; Carel B. Hoyng; Manuel Benjamin B. Ibanez; Chris F. Inglehearn; Takeshi Iwata; Brynjar O. Jensson; Kaylie Jones; Vasiliki Kalatzis; Smaragda Kamakari; Marianthi Karali; Ulrich Kellner; Caroline C. W. Klaver; Krisztina Knézy; Robert K. Koenekoop; Susanne Kohl; Taro Kominami; Laura Kühlewein; Tina M. Lamey; Rina Leibu; Bart P. Leroy; Petra Liskova; Irma Lopez; Victor R. de J. López-Rodríguez; Quinten Mahieu; Omar A. Mahroo; Gaël Manes; Luke Mansard; M. Pilar Martín-Gutiérrez; Nelson Martins; Laura Mauring; Martin McKibbin; Terri L. McLaren; Isabelle Meunier; Michel Michaelides; José M. Millán; Kei Mizobuchi; Rajarshi Mukherjee; Zoltán Zsolt Nagy; Kornelia Neveling; Monika Ołdak; Michiel Oorsprong; Yang Pan; Anastasia Papachristou; Antonio Percesepe; Maximilian Pfau; Eric A. Pierce; Emily Place; Raj Ramesar; Francis Ramond; Florence Andrée Rasquin; Gillian I. Rice; Lisa Roberts; María Rodríguez-Hidalgo; Javier Ruiz-Ederra; Ataf H. Sabir; Ai Fujita Sajiki; Ana Isabel Sánchez-Barbero; Asodu Sandeep Sarma; Riccardo Sangermano; Cristina M. Santos; Margherita Scarpato; Hendrik P. N. Scholl; Dror Sharon; Sabrina G. Signorini; Francesca Simonelli; Ana Berta Sousa; Maria Stefaniotou; Kari Stefansson; Katarina Stingl; Akiko Suga; Patrick Sulem; Lori S. Sullivan; Viktória Szabó; Jacek P. Szaflik; Gita Taurina; Alberta A. H. J. Thiadens; Carmel Toomes; Viet H. Tran; Miltiadis K. Tsilimbaris; Pavlina Tsoka; Veronika Vaclavik; Marie Vajter; Sandra Valeina; Enza Maria Valente; Casey Valentine; Rebeca Valero; Sophie Valleix; Joseph van Aerschot; L. Ingeborgh van den Born; Mattias Van Heetvelde; Virginie J. M. Verhoeven; Andrea L. Vincent; Andrew R. Webster; Laura Whelan; Bernd Wissinger; Georgia G. Yioti; Kazutoshi Yoshitake; Juan C. Zenteno; Roberta Zeuli; Theresia Zuleger; Chaim Landau; Allan I. Jacob; Siying Lin; Frans P. M. Cremers; Winston Lee; Jamie M. Ellingford; David Stanek; Susanne Roosing; Carlo Rivolta
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Genetic Spectrum of Negative Electroretinograms in a Predominantly Pediatric Cohort of 177 Patients
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2025-12-01
err0
errOAAI
errZaslavsky, Kirill; Tumber, Anupreet; Millar, Eoghan; Boginskaia, Olga; Macdonald, Heather; Klatt, Regan; Ali, Asim; Heon, Elise; Vincent, Ajoy
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errSave
CEP76 impairment at the centrosome-cilium interface contributes to a spectrum of ciliopathies
errScience Advances
IF12.5
err2025-10-17
err0
PREAI
errKamal Khan; Erika Tavares; Katherine Bishara; Aysegul Ozanturk; Leila Qebibo; Stephan Frangakis; Daniel G. Calame; Isabelle Meunier; Béatrice Bocquet; Rafal Ploski; Mohammad Ayman Al Khateeb; Dana Marafi; Luke Mansard; Lena Damaj; Richard A. Lewis; Farid Ullah; Thomas Arbogast; Jackson P. Ogden; Madeleine Harion; Marjolaine Willems; Maha S. Zaki; Tobias Bartolomaeus; Anne-Françoise Roux; James R. Lupski; Malgorzata Rydzanicz; Rami Abou Jamra; Francis Ramond; Elise Heon; Lydie Burglen; Erica E. Davis
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BASELINE VISUAL FIELD FINDINGS IN THE RUSH2A STUDY: ASSOCIATED FACTORS AND CORRELATION WITH OTHER MEASURES OF DISEASE SEVERITY (vol 219, pg 87, 2020)
errAMERICAN JOURNAL OF OPHTHALMOLOGY
IF4.2
err2025-05-01
err0
PREAI
errDuncan, JL; Liang, WD; Maguire, MG; Audo, I; Ayala, AR; Birch, DG; Carroll, J; Cheetham, JK; Degli Esposti, S; Durham, TA; Erker, L; Farsiu, S; Ferris, FL III; Heon, E; Hufnagel, RB; Iannacconé, A; Jaffe, GJ; Kay, CN; Michaelides, M; Pennesi, ME; Sahel, JA
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errSave
Defective IFT57 underlies a novel cause of Bardet-Biedl syndrome
errHUMAN MOLECULAR GENETICS
IF3.2
err2025-04-24
err0
errOAAI
errNitoiu, Alexandra; Zhang, Qihong; Tavares, Erika; Li, Janice Min; Ahmed, Kashif; Green-Sanderson, Kit; Rashid, Mahnoor; Morcos, Shahir M.; Maynes, Jayson T.; Campos, Eric, I; Sheffield, Val C.; Vincent, Ajoy; Heon, Elise
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errSave
Variants in CFAP410 cause a range of retinal and skeletal phenotypes
errNPJ GENOMIC MEDICINE
IF4.8
err2025-04-17
err0
errOAAI
errSchmidt, Ryan E.; Pohodich, Amy E.; Birch, David; Jones, Kaylie; Lam, Byron L.; Jung, Emily H.; Jain, Nieraj; Georgiou, Michalis; Mahroo, Omar A.; Webster, Andrew R.; Michaelides, Michel; Bakall, Benjamin; Iannaccone, Alessandro; Vincent, Ajoy; Parameswarappa, Deepika C.; Heon, Elise; Scholl, Hendrik P. N.; Janeschitz-Kriegl, Lucas; Traboulsi, Elias I.; Zein, Wadih; Brooks, Brian P.; Cukras, Catherine; Hufnagel, Robert; Aleman, Tomas S.; Sylla, Mohamed M.; Tsang, Stephen H.; Alabek, Michelle; Sahel, Jose; Gorin, Michael B.; van Genderen, Maria M.; Stingl, Katarina; Reith, Milda; Kohl, Susanne; Amaral, Rebeca Azevedo Souza; Sallum, Juliana Maria Ferraz; Vincent, Andrea L.; Hull, Sarah; Duncan, Jacque L.; Hanson, James V. M.; Tedeus, Matthias; Maggi, Jordi; Graf, Urs; Koller, Samuel; Berger, Wolfgang; Gerth-Kahlert, Christina; Marra, Molly; Everett, Lesley A.; Yang, Paul; Pennesi, Mark E.
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errSave
Insights into the effects of subretinal voretigene neparvovec-rzyl in RPE65-associated Leber congenital amaurosis
errCanadian Journal of Ophthalmology
IF0
err2025-02-05
err0
errOAAI
errAlaa Tayyib; Deepika C. Parameswarappa; Peter J. Kertes; Rajeev Muni; Anupreet Tumber; Gregory Costain; Alex Schramm; Heather MacDonald; Regan Klatt; Ajoy Vincent; Elise Héon
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errSave
“Blindness” is not a contraindication for voretigene neparvovec-rzyl treatment: a review of 9 cases
errCanadian Journal of Ophthalmology
IF0
err2025-01-15
err0
errOAAI
errDeepika C. Parameswarappa; Kirk A.J. Stephenson; Mark Seamone; Cynthia X. Qian; Rajeev H. Muni; Peter J. Kertes; Ajoy Vincent; Elise Héon
errShare
errSave
From Cellular to Metabolic: Advances in Imaging of Inherited Retinal Diseases
errDIAGNOSTICS
IF3.3
err2024-12-26
err0
errOAAI
errParameswarappa, Deepika C.; Kulkarni, Ashwini; Sahoo, Niroj Kumar; Padhy, Srikanta Kumar; Singh, Sumit Randhir; Heon, Elise; Chhablani, Jay
errShare
errSave
Autosomal-dominant macular dystrophy linked to a chromosome 17 tandem duplication
errJCI INSIGHT
IF6.1
err2024-12-06
err0
errOAAI
errAdele, Rabiat; Hussein, Rowaida; Tavares, Erika; Ahmed, Kashif; Di Scipio, Matteo; Charish, Jason; Liang, Minggao; Monis, Simon; Tumber, Anupreet; Chen, Xiaoyan; Paton, Tara A.; Roslin, Nicole M.; Eileen, Christabel; Ivakine, Evgueni; Sunny, Nishanth E.; Wilson, Michael D.; Campos, Eric; Rajala, Raju V. S.; Maynes, Jason T.; Monnier, Philippe P.; Paterson, Andrew D.; Heon, Elise; Vincent, Ajoy
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errSave
Therapies for Inherited Retinal Dystrophies: What is Enough?
errDRUG DISCOVERY TODAY
IF7.5
err2024-09-01
err2
PREAI
errLeroy, Bart P.; Daly, Avril; Heon, Elise; Sahel, Jose-Alain; Dollfus, Helene
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errSave
Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study
errBRITISH JOURNAL OF OPHTHALMOLOGY
IF3.5
err2024-07-30
err2
PREAI
errIgelman, Austin D.; White, Elizabeth; Tayyib, Alaa; Everett, Lesley; Vincent, Ajoy; Heon, Elise; Zeitz, Christina; Michaelides, Michel; Mahroo, Omar A.; Katta, Mohamed; Webster, Andrew; Preising, Markus; Lorenz, Birgit; Khateb, Samer; Banin, Eyal; Sharon, Dror; Luski, Shahar; Van Den Broeck, Filip; Leroy, Bart Peter; De Baere, Elfride; Walraedt, Sophie; Stingl, Katarina; Kuehlewein, Laura; Kohl, Susanne; Reith, Milda; Fulton, Anne; Raghuram, Aparna; Meunier, Isabelle; Dollfus, Helene; Aleman, Tomas S.; Bedoukian, Emma C.; O'Neil, Erin C.; Krauss, Emily; Vincent, Andrea; Jordan, Charlotte; Iannaccone, Alessandro; Sen, Parveen; Sundaramurthy, Srilekha; Nagasamy, Soumittra; Balikova, Irina; Casteels, Ingele; Borooah, Shyamanga; Yassin, Shaden; Nagiel, Aaron; Schwartz, Hillary; Zanlonghi, Xavier; Gottlob, Irene; Mclean, Rebecca J.; Munier, Francis L.; Stephenson, Andrew; Sisk, Robert; Koenekoop, Robert; Wilson, Lorri B.; Fredrick, Douglas; Choi, Dongseok; Yang, Paul; Pennesi, Mark Edward
errShare
errSave
Functional Vision in Patients With Biallelic USH2A Variants
errAMERICAN JOURNAL OF OPHTHALMOLOGY
IF4.2
err2024-04-01
err0
PREAI
errHeon, Elise; Melia, Michele; Bocchino, Laura E.; Samarakoon, Lassana; Duncan, Jacque L.; Ayala, Allison R.; Audo, Isabelle; Bradley, Chris; Cheetham, Janet K.; Dagnelie, Gislin; Durham, Todd A.; Hoyng, Carel B.; Jain, Nieraj; Jayasundera, Kanishka T.; Pennesi, Mark E.; Weng, Christina Y.
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errSave
Treatment Strategy With Gene Editing for Late-Onset Retinal Degeneration Caused by a Founder Variant in C1QTNF5
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2023-12-22
err2
errOAAI
errLi, Randa T. H.; Roman, Alejandro J.; Sumaroka, Alexander; Stanton, Chloe M.; Swider, Malgorzata; Garafalo, Alexandra V.; Heon, Elise; Vincent, Ajoy; Wright, Alan F.; Megaw, Roly; Aleman, Tomas S.; Browning, Andrew C.; Dhillon, Baljean; Cideciyan, Artur V.
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errSave
KCNV2-associated retinopathy: genotype-phenotype correlations-KCNV2 study group report 3
errBRITISH JOURNAL OF OPHTHALMOLOGY
IF3.5
err2023-10-18
err1
errOAAI
errde Guimaraes, Thales A. C.; Georgiou, Michalis; Robson, Anthony G.; Fujinami, Kaoru; Vincent, Ajoy; Nasser, Fadi; Khateb, Samer; Mahroo, Omar A.; Pontikos, Nikolas; Vargas, Mauricio E.; Thiadens, Alberta A. H. J.; de Carvalho, Emanuel R.; Nguyen, Xuan-Than-An; Arno, Gavin; Fujinami-Yokokawa, Yu; Liu, Xiao; Tsunoda, Kazushige; Hayashi, Takaaki; Jimenez-Rolando, Belen; Martin-Merida, Maria Inmaculada; Avila-Fernandez, Almudena; Salas, Ester Carreno; Garcia-Sandoval, Blanca; Ayuso, Carmen; Sharon, Dror; Kohl, Susanne; Huckfeldt, Rachel M.; Banin, Eyal; Pennesi, Mark E.; Khan, Arif O.; Wissinger, Bernd; Webster, Andrew R.; Heon, Elise; Boon, Camiel J. F.; Zrenner, Eberhard; Michaelides, Michel
errShare
errSave
Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction
errHUMAN GENETICS AND GENOMICS ADVANCES
IF3.6
err2023-04-01
err14
errOAAI
errReurink, Janine; Weisschuh, Nicole; Garanto, Alejandro; Dockery, Adrian; van den Born, L. Ingeborgh; Fajardy, Isabelle; Haer-Wigman, Lonneke; Kohl, Susanne; Wissinger, Bernd; Farrar, G. Jane; Ben-Yosef, Tamar; Pfiffner, Fatma Kivrak; Berger, Wolfgang; Weener, Marianna E.; Dudakova, Lubica; Liskova, Petra; Sharon, Dror; Salameh, Manar; Offenheim, Ashley; Heon, Elise; Girotto, Giorgia; Gasparini, Paolo; Morgan, Anna; Bergen, Arthur A.; ten Brink, Jacoline B.; Klaver, Caroline C. W.; Tranebjaerg, Lisbeth; Rendtorff, Nanna D.; Vermeer, Sascha; Smits, Jeroen J.; Pennings, Ronald J. E.; Aben, Marco; Oostrik, Jaap; Astuti, Galuh D. N.; Galbany, Jordi Corominas; Kroes, Hester Y.; Phan, Milan; Zelst-Stams, Wendy A. G. van; Thiadens, Alberta A. H. J.; Verheij, Joke B. G. M.; Schooneveld, Mary J. van; Bruijn, Suzanne E. de; Li, Catherina H. Z.; Hoyng, Carel B.; Gilissen, Christian; Vissers, Lisenka E. L. M.; Cremers, Frans P. M.; Kremer, Hannie; van Wijk, Erwin; Roosing, Susanne
errShare
errSave
Shedding light on myopia by studying complete congenital stationary night blindness
errPROGRESS IN RETINAL AND EYE RESEARCH
IF14.7
err2023-03-01
err12
errOAAI
errZeitz, Christina; Roger, Jerome E.; Audo, Isabelle; Michiels, Christelle; Sanchez-Farias, Nuria; Varin, Juliette; Frederiksen, Helen; Wilmet, Baptiste; Callebert, Jacques; Gimenez, Marie-Laure; Bouzidi, Nassima; Blond, Frederic; Guilllonneau, Xavier; Fouquet, Stephane; Leveillard, Thierry; Smirnov, Vasily; Vincent, Ajoy; Heon, Elise; Sahela, Jose-Alain; Kloeckener-Gruissemi, Barbara; Sennlaub, Florian; Morgansj, Catherine W.; Duvoisinj, Robert M.; V. Tkatchenko, Andrei; Picaud, Serge
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errSave
Photoreceptor Function and Structure in Autosomal Dominant Vitelliform Macular Dystrophy Caused by BEST1 Mutations
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2022-12-13
err1
errOAAI
errCideciyan, Artur V.; Jacobson, Samuel G.; Swider, Malgorzata; Sumaroka, Alexander; Sheplock, Rebecca; Krishnan, Arun K.; Garafalo, Alexandra V.; Guziewicz, Karina E.; Aguirre, Gustavo D.; Beltran, William A.; Heon, Elise
errShare
errSave
Baseline Microperimetry and OCT in the RUSH2A Study: Structure -Function Association and Correlation With Disease Severity
errAMERICAN JOURNAL OF OPHTHALMOLOGY
IF4.2
err2022-12-01
err21
errOAAI
errLad, Eleonora M.; Duncan, Jacque L.; Liang, Wendi; Maguire, Maureen G.; Ayala, Allison R.; Audo, Isabelle; Birch, David G.; Carroll, Joseph; Cheetham, Janet K.; Durham, Todd A.; Fahim, Abigail T.; Loo, Jessica; Deng, Zengtian; Mukherjee, Dibyendu; Heon, Elise; Hufnagel, Robert B.; Guan, Bin; Iannaccone, Alessandro; Jaffe, Glenn J.; Kay, Christine N.; Michaelides, Michel; Pennesi, Mark E.; Vincent, Ajoy; Weng, Christina Y.; Farsiu, Sina
errShare
errSave

Research Directions

No research directions
Co-authors
Cooperation Journals
T
Tien Yin Wong
H-index: 208 · Papers: 3.1K
S
Stephen W. Scherer
H-index: 161 · Papers: 1.1K
J
James M. Wilson
H-index: 155 · Papers: 1.4K
J
James R. Lupski
H-index: 144 · Papers: 1.1K
M
Mark A. Tarnopolsky
H-index: 129 · Papers: 889
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