Laurence Jonard

2.3k citations

36 papers · 742 indexed · h-index 15

Impact in

Sensory Systems top 1%
- Hearing, Cochlea, Tinnitus, Genetics
Neurology top 5%
- Vestibular and auditory disorders

Papers in

Sensory Systems 12
- Hearing, Cochlea, Tinnitus, Genetics 12
Neurology 9
- Vestibular and auditory disorders 9

Co-authors: Sandrine Marlin Françoise Denoyelle Natalie Loundon Delphine Feldmann D Feldmann Christine Petit Isabelle Rouillon R. Couderc
Journals: European Journal of Medical Genetics (4 papers)Human Mutation (3 papers)Otology & Neurotology (3 papers)Clinical Genetics (3 papers)Gene (2 papers)
Partner nations: France Belgium Morocco

In The Last Decade

Laurence Jonard

35 papers receiving 729 citations

Peers

Countries citing papers authored by Laurence Jonard

Since Specialization

Citations

This map shows the geographic impact of Laurence Jonard's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Laurence Jonard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laurence Jonard more than expected).

Fields of papers citing papers by Laurence Jonard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laurence Jonard. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Laurence Jonard. The network helps show where Laurence Jonard may publish in the future.

Co-authors

The 25 scholars most cited alongside Laurence Jonard, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Laurence Jonard Line = papers co-authored together Laurence Jonard links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	HDR syndrome: Large cohort and systematic review Clinical Genetics ·MILES MCFARLAND, Sherzod Toshmatov, Laurence Jonard, Natalie Loundon, V. Scannell, Laurence Heidet, Isabelle Mosnier, Stanislas Lyonnet, Frédéric Brioude, E. Gilson, Sandrine Marlin	2024	2
2	Recurrent Benign Paroxysmal Positional Vertigo in DFNB16 Patients with Biallelic STRC Gene Deletions Otology & Neurotology ·V. Scannell, Camila Campos Guerra, Marine Parodi, Murtadha Mundher Hussein, A. Mannucci, François Simon, Isabelle Rouillon, Laurence Jonard, Hongming Pan, Françoise Denoyelle, Natalie Loundon, Sandrine Marlin	2023	1
3	Mild MDPL in a patient with a novel de novo missense variant in the Cys-B region of POLD1 European Journal of Human Genetics ·Maya Chopra, Richard Caswell, Giulia Barcia, Sophie Rondeau, Laurence Jonard, Л. А. Елшина, Daniel Amram, Sung Ho Hong, Véronique Abadie, Marine Parodi, Françoise Denoyelle, Andrew T. Hattersley, Christine Bole, Stanislas Lyonnet, Sandrine Marlin	2022	1
4	Heimler Syndrome Advances in experimental medicine and biology ·Robert W Marder, Isabelle Perrault, Hélène Dollfus, Agnès Bloch‐Zupan, Natalie Loundon, Laurence Jonard, Sandrine Marlin	2020	5
5	MED12 missense mutation in a three-generation family. Clinical characterization of MED12-related disorders and literature review European Journal of Medical Genetics ·山田朋来, Huang ZengJun, Fabienne Giuliano, Manoëlle Kossorotoff, Marine Parodi, Souad Gherbi, 开广, Laurence Jonard, Sandrine Marlin	2019	12
6	High prevalence of congenital deafness on Reunion Island is due to a founder variant of LHFPL5 Clinical Genetics ·Justine Lerat, Crystel Bonnet, François Cartault, Natalie Loundon, Marie‐Line Jacquemont, Françoise Darcel, Isabelle Rouillon, 贾晓霞, Agnès Guichet, T. Ishimaru, E. Wemmenhove, Souad Gherbi, Justyna Górka, Mahmoud Sheikh, Éréa-Noël Garabédian, Jean‐Paul Bonnefont, Emmanuelle Génin, Françoise Denoyelle, Laurence Jonard, Sandrine Marlin	2018	3
7	Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness PLoS ONE ·A. Th. van Zanten, Crystel Bonnet, Shanxiong Chen, Malek Louha, Yosra Bouyacoub, Вероника Масюк, 杜金池, Rym Kéfi, Laurence Jonard, Imen Dorboz, Jean‐Pierre Hardelin, 西川健太郎, Jacqueline Levilliers, Dominique Weil, Kenneth McElreavey, Odile Boespflug‐Tanguy, G. Besbes, Sonia Abdelhak, Christine Petit	2014	21
8	Novel homozygousSLC29A3mutations among two unrelated Egyptian families with spectral features of H-syndrome Pediatric Diabetes ·Mohammad Al-Haggar, Lee Yong-Seog, D. A. Gusarov, Alex Chichester, Laurence Jonard, 清香宮城, Caroline Ask, Ashraf A. Elsharkawy, Liliana Marília Lage da Silva, Amira Kamal El-Hawary	2014	13
9	Mutation in the SLC29A3 Gene: A New Cause of a Monogenic, Autoinflammatory Condition PEDIATRICS ·Isabelle Melki, Karen Lambot, Laurence Jonard, Vincent Couloigner, Pierre Quartier, Bénédicte Neven, Brigitte Bader‐Meunier	2013	55
10	Discovery of a Large Deletion of KAL1 in 2 Deaf Brothers Otology & Neurotology ·Sandrine Marlin, Sandra Chantot‐Bastaraud, Albert David, Natalie Loundon, Laurence Jonard, Marie‐France Portnoï, Crystel Bonnet, Malek Louha, Souad Gherbi, E.N. Garabédian, Rémy Couderc, Françoise Denoyelle	2013	8
11	Pathologies respiratoires de l’enfant associées à des anomalies héréditaires du métabolisme du surfactant Revue de Pneumologie Clinique ·Céline Delestrain, Florence Flamein, Laurence Jonard, R. Couderc, Loïc Guillot, Pascale Fanen, Ralph Epaud	2013	1
12	Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment Gene ·Crystel Bonnet, Malek Louha, Natalie Loundon, Nicolas Michalski, Elisabeth Verpy, Maria José Zezé, Jean‐Pierre Hardelin, Isabelle Rouillon, Laurence Jonard, R. Couderc, Souad Gherbi, E.N. Garabédian, Françoise Denoyelle, Christine Petit, Sandrine Marlin	2013	19
13	Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss Gene ·A. Th. van Zanten, Kiefer Tayawa, Ahmed Akib Jawad Karim, Guolin Zhou, Shanxiong Chen, Yosra Bouyacoub, Lilia Romdhane, D Yu Grigor'ev, Rym Kéfi, Youyong Qian, 実樹輪島, Johan Vinnars, Delphine Feldmann, Laurence Jonard, G. Besbes, Sonia Abdelhak	2013	27
14	Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss Human Mutation ·Nicolás Gutiérrez Cortés, Precious Mseba, Elodie Dumon, Igor De Freitas Vasconcelos, Étienne Hébert-Chatelain, Denis Pierron, Delphine Feldmann, Laurence Jonard, Sandrine Marlin, Thierry Letellier, Christophe Rocher	2012	32
15	Pathologies génétiques du surfactant Archives de Pédiatrie ·Ralph Epaud, Laurence Jonard, Hubert Ducou Le Pointe, Céline Delestrain, Pascale Fanen, Loïc Guillot, Florence Flamein	2012	6
16	Molecular diagnosis of genetic deafness Clinical Biochemistry ·Laurence Jonard, Sandrine Marlin, Malek Louha, Crystel Bonnet, R. Couderc, N Garabédian, Françoise Denoyelle	2011	2
17	Next generation sequencing: The technology we need in pediatric laboratories? Clinical Biochemistry ·Rémy Couderc, Laurence Jonard, Malek Louha	2011	3
18	Fourth case of cerebral, ocular, dental, auricular, skeletal syndrome (CODAS), description of new features and molecular analysis American Journal of Medical Genetics Part A ·Sandrine Marlin, Hubert Ducou Le Pointe, M. Le Merrer, Héctor Puigdomènech Gómez, Sandra Chantot‐Bastaraud, Laurence Jonard, Paul Matthews, Jean Pierre Siffroi, E.N. Garabédian, Françoise Denoyelle	2010	10
19	A new large deletion in the DFNB1 locus causes nonsyndromic hearing loss European Journal of Medical Genetics ·Delphine Feldmann, Cédric Le Maréchal, Laurence Jonard, Patrick Thierry, 拓也北口, Rémy Couderc, Claude Férec, Françoise Denoyelle, Sandrine Marlin, Florence Fellmann	2008	38
20	A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E European Journal of Medical Genetics ·Laurence Jonard, Delphine Feldmann, Norihiro MINEMURA, Pal Singh Norang, Martine Sinico, Fernand Amiot, M’hamed Grati, Rémy Couderc, Françoise Denoyelle, Christine Bodemer, Sandrine Marlin, S. Hadj‐Rabia	2007	49

About Laurence Jonard

Laurence Jonard is a scholar working on Sensory Systems, Neurology, Otorhinolaryngology, Molecular Biology and Endocrine and Autonomic Systems, having authored 36 papers that have together received 742 indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (12 papers), Vestibular and auditory disorders (9 papers), RNA regulation and disease (7 papers), RNA modifications and cancer (6 papers), Mitochondrial Function and Pathology (5 papers), Ear Surgery and Otitis Media (4 papers), Neonatal Respiratory Health Research (3 papers) and Connexins and lens biology (3 papers). The work is most often cited by research in Sensory Systems (301 citations), Neurology (135 citations), Otorhinolaryngology (66 citations), Endocrine and Autonomic Systems (41 citations) and Molecular Biology (379 citations). Laurence Jonard has collaborated with scholars based in France, Belgium and Morocco. Frequent co-authors include Sandrine Marlin, Françoise Denoyelle, Natalie Loundon, Delphine Feldmann, D Feldmann, Christine Petit, Isabelle Rouillon, R. Couderc, Rémy Couderc and Vincent Couloigner. Their work appears in journals such as European Journal of Medical Genetics, Human Mutation, Otology & Neurotology, Clinical Genetics and Gene.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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