A.L. Mosca

636 total citations
8 papers, 69 citations indexed

About

A.L. Mosca is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, A.L. Mosca has authored 8 papers receiving a total of 69 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in A.L. Mosca's work include Genomic variations and chromosomal abnormalities (6 papers), Genetic Syndromes and Imprinting (2 papers) and Congenital heart defects research (2 papers). A.L. Mosca is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genetic Syndromes and Imprinting (2 papers) and Congenital heart defects research (2 papers). A.L. Mosca collaborates with scholars based in France. A.L. Mosca's co-authors include Patrick Callier, Francine Mugneret, Laurence Faivre, Frédéric Huet, Nathalie Marle, Alice Masurel‐Paulet, Christel Thauvin‐Robinet, J. Teyssier, Simon Guiraud and Louise Joly and has published in prestigious journals such as American Journal of Medical Genetics Part A and European Journal of Medical Genetics.

In The Last Decade

A.L. Mosca

8 papers receiving 68 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A.L. Mosca France	6	61	30	18	12	8	8	69
Simon Zwolinski United Kingdom	4	70 1.1×	27 0.9×	12 0.7×	14 1.2×	9 1.1×	5	91
C Schluth France	7	79 1.3×	48 1.6×	38 2.1×	7 0.6×	6 0.8×	8	104
Debra Rita United States	4	50 0.8×	32 1.1×	32 1.8×	6 0.5×	3 0.4×	5	78
Anna Wilsdon United Kingdom	3	40 0.7×	42 1.4×	10 0.6×	10 0.8×	5 0.6×	6	76
Marine Lebrun France	5	46 0.8×	39 1.3×	14 0.8×	12 1.0×	3 0.4×	9	78
Valerie Banks United States	3	56 0.9×	56 1.9×	10 0.6×	9 0.8×	6 0.8×	3	77
Jayson Rodriguez United States	3	39 0.6×	25 0.8×	10 0.6×	7 0.6×	5 0.6×	4	52
Rosa Baldinger Switzerland	5	54 0.9×	41 1.4×	36 2.0×	4 0.3×	5 0.6×	5	90
Ikeoluwa Osei‐Owusu United States	2	32 0.5×	28 0.9×	11 0.6×	5 0.4×	5 0.6×	4	57
Isolde Schreyer Germany	5	69 1.1×	30 1.0×	32 1.8×	28 2.3×	2 0.3×	10	87

Countries citing papers authored by A.L. Mosca

Since Specialization

Citations

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

Fields of papers citing papers by A.L. Mosca

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A.L. Mosca. 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 A.L. Mosca. The network helps show where A.L. Mosca may publish in the future.

Co-authorship network of co-authors of A.L. Mosca

This figure shows the co-authorship network connecting the top 25 collaborators of A.L. Mosca. A scholar is included among the top collaborators of A.L. Mosca 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 A.L. Mosca. A.L. Mosca is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

Mosca, A.L., Patrick Callier, Laurence Faivre, et al.. (2011). A prenatal case of inverted duplication with terminal deletion of 5p not including the cat‐like cry critical region. American Journal of Medical Genetics Part A. 155(8). 2031–2034. 2 indexed citations

Mosca, A.L., Patrick Callier, Alice Masurel‐Paulet, et al.. (2010). Cytogenetic and array‐CGH characterization of a 6q27 deletion in a patient with developmental delay and features of Ehlers–Danlos syndrome. American Journal of Medical Genetics Part A. 152A(5). 1314–1317. 7 indexed citations

Mosca, A.L., Patrick Callier, Laurence Faivre, et al.. (2009). Polymicrogyria in a child with inv dup del(9p) and 22q11.2 microduplication. American Journal of Medical Genetics Part A. 149A(3). 475–481. 13 indexed citations

Callier, Patrick, Laurence Faivre, Nathalie Marle, et al.. (2009). Detection of an interstitial 3q21.1‐q21.3 deletion in a child with multiple congenital abnormalities, mental retardation, pancytopenia, and myelodysplasia. American Journal of Medical Genetics Part A. 149A(6). 1323–1326. 8 indexed citations

Callier, Patrick, Laurence Faivre, Christel Thauvin‐Robinet, et al.. (2008). Array‐CGH in a series of 30 patients with mental retardation, dysmorphic features, and congenital malformations detected an interstitial 1p22.2‐p31.1 deletion in a patient with features overlapping the Goldenhar syndrome. American Journal of Medical Genetics Part A. 146A(16). 2109–2115. 20 indexed citations

Mosca, A.L., Patrick Callier, Bruno Leheup, et al.. (2007). Fortuitous FISH diagnosis of an interstitial microdeletion (5)(q31.1q31.2) in a girl suspected to present a cri‐du‐chat syndrome. American Journal of Medical Genetics Part A. 143A(12). 1342–1347. 7 indexed citations

Callier, Patrick, Laurence Faivre, Nathalie Marle, et al.. (2007). Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip–palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24). European Journal of Medical Genetics. 50(6). 455–464. 9 indexed citations

Mosca, A.L., Nicole Laurent, Laurent Guibaud, et al.. (2006). Polymicrogyria, cerebellar vermis hypoplasia, severe facial dysmorphism and cleft palate: a new syndrome?. European Journal of Medical Genetics. 50(1). 48–53. 3 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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