Alice Goldenberg

7.2k citations
49 papers · 1.3k · h-index 20

Impact in

  • Genetics top 5%
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Connective tissue disorders research
  • Developmental Biology top 10%

Papers in

  • Molecular Biology 27
    • Congenital heart defects research 4
    • RNA modifications and cancer 4
    • Epigenetics and DNA Methylation 3
  • Genetics 21
    • Genomic variations and chromosomal abnormalities 9
    • Genetics and Neurodevelopmental Disorders 6
Co-authors
Valérie Cormier‐Daire (9 shared papers)Pascale Saugier-Véber (11 shared papers)Arnold Münnich (6 shared papers)Caroline Michot (4 shared papers)Thierry Frébourg (10 shared papers)Marlène Rio (2 shared papers)Muriel Holder‐Espinasse (4 shared papers)Geneviève Baujat (4 shared papers)
Journals
European Journal of Human Genetics (5 papers)Human Mutation (4 papers)Journal of Medical Genetics (3 papers)European Journal of Medical Genetics (2 papers)Pediatric Nephrology (2 papers)
Partner nations
FranceSwitzerlandUnited States

In The Last Decade

Alice Goldenberg

48 papers receiving 1.3k citations

Peers

Alice Goldenberg
Comparison fields: 5 of 79
  • Genetics 526
  • Developmental Biology 34
  • Molecular Biology 744
  • Cellular and Molecular Neuroscience 120
  • Clinical Biochemistry 43
Replace Tommaso Pippucci with:
Tommaso Pippucci Italy
Victoria Mok Siu Canada
Boris Keren France
Holger Tönnies Germany
Delphine Héron France
Sibel Kantarci United States
Ghada M. H. Abdel‐Salam Egypt
Elizabeth Roeder United States
Ewa Obersztyn Poland
David Geneviève France
Alice Goldenberg relative to Tommaso Pippucci Italy Tommaso Pippucci's profile →
Citations per field
00.5×1.7×
Tommaso Pippucci · 1×
Citations per year

Countries citing papers authored by Alice Goldenberg

Since Specialization
Citations

This map shows the geographic impact of Alice Goldenberg'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 Alice Goldenberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alice Goldenberg more than expected).

Fields of papers citing papers by Alice Goldenberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alice Goldenberg. 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 Alice Goldenberg. The network helps show where Alice Goldenberg may publish in the future.

Co-authors

The 25 scholars most cited alongside Alice Goldenberg, 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 Alice Goldenberg Line = papers co-authored together Alice Goldenberg links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 49 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Cardio-facio-cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling pathway: genotype–phenotype relationships and overlap with Costello syndrome
Journal of Medical Genetics ·Caroline Nava, Nadine Hanna, Caroline Michot, (unknown), Nathalie Pouvreau, Tetsuya Niihori, (unknown), Yoichi Matsubara, Benoı̂t Arveiler, Didier Lacombe, Éric Pasmant, B. Parfait, Clarisse Baumann, Delphine Héron, S. Sigaudy, Annick Toutain, Marlène Rio, Alice Goldenberg, Bruno Leheup, Alain Verloès, Hélène Cavé
2007173
2
MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations
Journal of Medical Genetics ·Nathalie Le Meur, Muriel Holder‐Espinasse, Sylvie Jaillard, Alice Goldenberg, Sylvie Joriot, Patrizia Amati‐Bonneau, Agnès Guichet, M. Barth, Aude Charollais, Hubert Journel, Stéphane Auvin, Cécile Boucher, (unknown), Véronique David, Sylvie Manouvrier‐Hanu, Pascale Saugier-Véber, Thierry Frébourg, Christèle Dubourg, Joris Andrieux, Dominique Bonneau
2009154
3
Natural history of Barth syndrome: a national cohort study of 22 patients
Orphanet Journal of Rare Diseases ·Charlotte Rigaud, Anne-Sophie Lèbre, Renaud Touraine, Blandine Beaupain, Chris Ottolenghi, A. Chabli, Hélène Ansquer, (unknown), Sylvie Di Filippo, Pascale de Lonlay, Betina Borm, François Rivier, Marie-Catherine Vaillant, Michèle Mathieu‐Dramard, Alice Goldenberg, Géraldine Viot, Philippe Charron, Marlène Rio, Damien Bonnet, Jean Donadieu
201398
4
Exome Sequencing Identifies PDE4D Mutations as Another Cause of Acrodysostosis
The American Journal of Human Genetics ·Caroline Michot, Carine Le Goff, Alice Goldenberg, Avinash Abhyankar, Céline Klein, Esther Kinning, Anne‐Marie Guerrot, Philippe Flahaut, A. Duncombe, Geneviève Baujat, Stanislas Lyonnet, Caroline Thalassinos, Patrick Nitschké, Jean‐Laurent Casanova, Martine Le Merrer, Arnold Münnich, Valérie Cormier‐Daire
201286
5
Mutational spectrum of CDKL5 in early‐onset encephalopathies: a study of a large collection of French patients and review of the literature
Clinical Genetics ·Christophe Némos, Laëtitia Lambert, Fabienne Giuliano, Bérénice Doray, A. Roubertie, Alice Goldenberg, B Delobel, Valérie Layet, M Ange N'guyen, Aline Saunier, F. Verneau, Philippe Jonveaux, Christophe Philippe
200984
6
Identification of Novel Craniofacial Regulatory Domains Located far Upstream ofSOX9and Disrupted in Pierre Robin Sequence
Human Mutation ·Christopher T. Gordon, Catia Attanasio, Shipra Bhatia, Sabina Benko, Morad Ansari, Tiong Yang Tan, Arnold Münnich, L Pennacchio, Véronique Abadie, I. Karen Temple, Alice Goldenberg, Veronica van Heyningen, Jeanne Amiel, David Fitzpatrick, Dirk A. Kleinjan, Axel Visel, Stanislas Lyonnet
201467
7
FAM46A mutations are responsible for autosomal recessive osteogenesis imperfecta
Journal of Medical Genetics ·Mathilde Doyard, Séverine Bacrot, Céline Huber, Maja Di Rocco, Alice Goldenberg, Mona Aglan, Perrine Brunelle, Samia A. Temtamy, Caroline Michot, Ghada A. Otaify, Coralie Haudry, Mireille Castanet, J. Leroux, Jean‐Paul Bonnefont, Arnold Münnich, Geneviève Baujat, Pablo Lapunzina, Sophie Monnot, Víctor L. Ruiz‐Pérez, Valérie Cormier‐Daire
201855
8
Juvenile Huntington disease in an 18-month-old boy revealed by global developmental delay and reduced cerebellar volume
American Journal of Medical Genetics Part A ·Gaël Nicolas, Didier Devys, Alice Goldenberg, David Maltête, Catherine Hervé, Didier Hannequin, Lucie Guyant‐Maréchal
201143
9
Human lissencephaly with cerebellar hypoplasia due to mutations in TUBA1A: expansion of the foetal neuropathological phenotype
Acta Neuropathologica ·Magalie Lecourtois, Karine Poirier, Gaëlle Friocourt, Xavier H. Jaglin, Alice Goldenberg, Pascale Saugier-Véber, Jamel Chelly, Annie Laquerrière
201039
10
Implication of non-coding PAX6 mutations in aniridia
Human Genetics ·Julie Plaisancié, M. Tarilonte, Patrícia Locosque Ramos, Claire Jeanton-Scaramouche, Véronique Gaston, Hélène Dollfus, Dora Aguilera, J.‐C. Kaplan, Lucas Fares‐Taie, Fiona Blanco‐Kelly, Cristina Villaverde, Christine Francannet, Alice Goldenberg, Ignacio Arroyo, Jean‐Michel Rozet, Carmen Ayuso, Nicolas Chassaing, Patrick Calvas, Marta Cortón
201834
11
Antenatal manifestations of Smith‐Lemli‐Opitz (RSH) syndrome: A retrospective survey of 30 cases
American Journal of Medical Genetics Part A ·Alice Goldenberg, Claude Wolf, Françoise Chevy, Alexandra Benachi, Yves Dumez, Arnold Münnich, Valérie Cormier‐Daire
200332
12
Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia
Molecular Psychiatry ·Boris Chaumette, Vladimir Ferrafiat, Amirthagowri Ambalavanan, Alice Goldenberg, Alexandre Dionne‐Laporte, Dan Spiegelman, Patrick A. Dion, Priscille Gérardin, Claudine Laurent, Doron Cohen, Judith L. Rapoport, Guy A. Rouleau
201829
13
Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes
European Journal of Human Genetics ·Sandy Léger, X. Balguérie, Alice Goldenberg, Valérie Drouin‐Garraud, Annick Cabot, Isabelle Amstutz-Montadert, Paul Young, P. Joly, Virginie Bodereau, Muriel Holder‐Espinasse, Robyn V. Jamieson, Amanda Krause, Hongsheng Chen, Clarisse Baumann, Luís Nunes, Hélène Dollfus, Michel Goossens, Véronique Pingault
201228
14
Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation
European Journal of Human Genetics ·Pascale Saugier-Véber, Alice Goldenberg, Valérie Drouin‐Garraud, Céline de La Rochebrochard, Valérie Layet, Nathalie Drouot, Nathalie Le Meur, Brigitte Gilbert‐Dussardier, Géraldine Joly‐Hélas, Hélène Moirot, Annick Rossi, Mario Tosi, Thierry Frébourg
200628
15
IL11RA‐related Crouzon‐like autosomal recessive craniosynostosis in 10 new patients: Resemblances and differences
Clinical Genetics ·Elise Brischoux‐Boucher, Aurélien Trimouille, Geneviève Baujat, Alice Goldenberg, Élise Schaefer, B. Guichard, P. Hannequin, Giovanna Paternoster, Sarah Baer, Christelle Cabrol, E. Weber, G. Godfrin, Marion Lenoir, Didier Lacombe, Corinne Collet, Lionel Van Maldergem
201826
16
Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene
Acta Neuropathologica Communications ·Pascale Saugier-Véber, Florent Marguet, François Lecoquierre, Homa Adle‐Biassette, Fabien Guimiot, Sara Cipriani, Sophie Patrier, M. Brasseur‐Daudruy, Alice Goldenberg, Valérie Layet, Yline Capri, Marion Gérard, Thierry Frébourg, Annie Laquerrière
201725
17
Protein-altering MYH3 variants are associated with a spectrum of phenotypes extending to spondylocarpotarsal synostosis syndrome
European Journal of Human Genetics ·Raphaël Carapito, Alice Goldenberg, Nicodème Paul, Angélique Pichot, Albert David, Antoine Hamel, Clémentine Dumant‐Forest, J. Leroux, Benjamin Ory, Bertrand Isidor, Seiamak Bahram
201624
18
Deletion 18q21.2q21.32 involving TCF4 in a boy diagnosed by CGH-array
European Journal of Medical Genetics ·Joris Andrieux, Frédéric Leprêtre, Jean‐Marie Cuisset, Alice Goldenberg, Bruno Delobel, Sylvie Manouvrier‐Hanu, Muriel Holder‐Espinasse
200822
19
Not All Floating-Harbor Syndrome Cases are Due to Mutations in Exon 34 ofSRCAP
Human Mutation ·Carine Le Goff, Clémentine Mahaut, Armand Bottani, Bérénice Doray, Alice Goldenberg, Anne Moncla, Sylvie Odent, Patrick Nitschké, Arnold Münnich, Laurence Faivre, Valérie Cormier‐Daire
201222
20
Dissecting the molecular mechanisms in craniofrontonasal syndrome: differential mRNA expression of mutant EFNB1 and the cellular mosaic
European Journal of Human Genetics ·Ilse Wieland, Román Makarov, William Reardon, Sigrid Tinschert, Alice Goldenberg, Patrick Thierry, Peter Wieacker
200720

About Alice Goldenberg

Alice Goldenberg is a scholar working on Molecular Biology, Genetics, Surgery, Pediatrics, Perinatology and Child Health and Cellular and Molecular Neuroscience, having authored 49 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (6 papers), Congenital heart defects research (4 papers), RNA modifications and cancer (4 papers), Cholesterol and Lipid Metabolism (3 papers), Epigenetics and DNA Methylation (3 papers), Prenatal Screening and Diagnostics (3 papers) and Congenital limb and hand anomalies (3 papers). The work is most often cited by research in Genetics (526 citations), Developmental Biology (34 citations), Molecular Biology (744 citations), Cellular and Molecular Neuroscience (120 citations) and Clinical Biochemistry (43 citations). Alice Goldenberg has collaborated with scholars based in France, Switzerland and United States. Frequent co-authors include Valérie Cormier‐Daire, Pascale Saugier-Véber, Arnold Münnich, Caroline Michot, Thierry Frébourg, Marlène Rio, Muriel Holder‐Espinasse, Geneviève Baujat, Joris Andrieux and Nathalie Le Meur. Their work appears in journals such as European Journal of Human Genetics, Human Mutation, Journal of Medical Genetics, European Journal of Medical Genetics and Pediatric Nephrology.

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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