Nada Houcinat

632 total citations
6 papers, 96 citations indexed

About

Nada Houcinat is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Nada Houcinat has authored 6 papers receiving a total of 96 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Nada Houcinat's work include Genetics and Neurodevelopmental Disorders (3 papers), Connective tissue disorders research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Nada Houcinat is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Connective tissue disorders research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Nada Houcinat collaborates with scholars based in France, Martinique and United States. Nada Houcinat's co-authors include Sébastien Moutton, Laurence Faivre, Dorothée Cailley, Antonio Vitobello, Christophe Philippe, Yannis Duffourd, Mirna Assoum, Benoı̂t Arveiler, Martin Chevarin and Didier Lacombe and has published in prestigious journals such as Human Mutation, European Journal of Human Genetics and Journal of Inherited Metabolic Disease.

In The Last Decade

Nada Houcinat

6 papers receiving 85 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Nada Houcinat France	5	70	39	16	16	10	6	96
Fathiya Al Murshedi Oman	6	56 0.8×	45 1.2×	8 0.5×	12 0.8×	16 1.6×	14	114
Alicia B. Byrne Australia	6	35 0.5×	46 1.2×	8 0.5×	9 0.6×	11 1.1×	8	91
Ilya Kanivets Russia	7	61 0.9×	91 2.3×	26 1.6×	29 1.8×	4 0.4×	39	162
Daisuke Ieda Japan	8	101 1.4×	103 2.6×	16 1.0×	9 0.6×	4 0.4×	16	164
Emanuela Ponzi Italy	7	93 1.3×	87 2.2×	22 1.4×	49 3.1×	5 0.5×	14	182
Lynette Rives United States	4	52 0.7×	33 0.8×	10 0.6×	5 0.3×	9 0.9×	7	97
Mihaela Pupavac Canada	8	44 0.6×	112 2.9×	13 0.8×	72 4.5×	10 1.0×	9	166
Nurit Assia Batzir Israel	5	43 0.6×	58 1.5×	11 0.7×	12 0.8×	4 0.4×	9	92
Thibaud Jouan France	5	57 0.8×	66 1.7×	9 0.6×	5 0.3×	11 1.1×	7	111
Özkan Özdemir Türkiye	7	47 0.7×	100 2.6×	9 0.6×	24 1.5×	8 0.8×	22	173

Countries citing papers authored by Nada Houcinat

Since Specialization

Citations

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

Fields of papers citing papers by Nada Houcinat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nada Houcinat

This figure shows the co-authorship network connecting the top 25 collaborators of Nada Houcinat. A scholar is included among the top collaborators of Nada Houcinat based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Nada Houcinat. Nada Houcinat is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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6 of 6 papers shown

1.

Bris, Céline, Vincent Procaccio, Patrizia Amati‐Bonneau, et al.. (2019). Deciphering exome sequencing data: Bringing mitochondrial DNA variants to light. Human Mutation. 40(12). 2430–2443. 7 indexed citations

2.

Bruel, Ange‐Line, Sophie Nambot, Antonio Vitobello, et al.. (2019). Increased diagnostic and new genes identification outcome using research reanalysis of singleton exome sequencing. European Journal of Human Genetics. 27(10). 1519–1531. 39 indexed citations

3.

Moutton, Sébastien, Ange‐Line Bruel, Mirna Assoum, et al.. (2018). Truncating variants of the DLG4 gene are responsible for intellectual disability with marfanoid features. Clinical Genetics. 93(6). 1172–1178. 17 indexed citations

4.

Kuster, Alice, Jean‐Baptiste Arnoux, Magalie Barth, et al.. (2017). Diagnostic approach to neurotransmitter monoamine disorders: experience from clinical, biochemical, and genetic profiles. Journal of Inherited Metabolic Disease. 41(1). 129–139. 11 indexed citations

5.

Vuillaume, Marie‐Laure, Nada Houcinat, Julie Bouron, et al.. (2017). First female prenatal case of osteopathia striata with cranial sclerosis in a fetus carrying a de-novo 1.9 Mbp interstitial deletion at Xq11.1q11.2. Clinical Dysmorphology. 26(4). 231–234. 1 indexed citations

6.

Houcinat, Nada, Brigitte Llanas, Sébastien Moutton, et al.. (2015). Homozygous 16p13.11 duplication associated with mild intellectual disability and urinary tract malformations in two siblings born from consanguineous parents. American Journal of Medical Genetics Part A. 167(11). 2714–2719. 21 indexed citations

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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