Annie Olry

4.6k total citations · 1 hit paper
8 papers, 1.1k citations indexed

About

Annie Olry is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Annie Olry has authored 8 papers receiving a total of 1.1k 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 Pulmonary and Respiratory Medicine. Recurrent topics in Annie Olry's work include Genomics and Rare Diseases (8 papers), Biomedical Text Mining and Ontologies (3 papers) and Cystic Fibrosis Research Advances (2 papers). Annie Olry is often cited by papers focused on Genomics and Rare Diseases (8 papers), Biomedical Text Mining and Ontologies (3 papers) and Cystic Fibrosis Research Advances (2 papers). Annie Olry collaborates with scholars based in France, United States and Germany. Annie Olry's co-authors include Ana Rath, Valérie Serrière-Lanneau, Charlotte Rodwell, Daniel N. Murphy, Stéphanie Nguengang Wakap, Deborah M. Lambert, Yann Le Cam, Ferdinand Dhombres, Bruno Urbero and Ségolène Aymé and has published in prestigious journals such as Human Mutation, Genetics in Medicine and European Journal of Human Genetics.

In The Last Decade

Annie Olry

7 papers receiving 1.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database

2019 833 citations Stéphanie Nguengang Wakap, Deborah M. Lambert et al. European Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Annie Olry France	4	633	438	107	86	80	8	1.1k
Daniel N. Murphy Ireland	7	573 0.9×	496 1.1×	103 1.0×	80 0.9×	73 0.9×	8	1.1k
Charlotte Rodwell France	5	551 0.9×	302 0.7×	115 1.1×	80 0.9×	78 1.0×	7	920
Valérie Serrière-Lanneau France	7	589 0.9×	484 1.1×	111 1.0×	91 1.1×	78 1.0×	11	1.6k
Stéphanie Nguengang Wakap France	4	494 0.8×	275 0.6×	101 0.9×	72 0.8×	70 0.9×	7	854
Yann Le Cam France	12	729 1.2×	400 0.9×	265 2.5×	119 1.4×	120 1.5×	25	1.4k
Mindy Clyne United States	17	526 0.8×	433 1.0×	55 0.5×	52 0.6×	17 0.2×	26	1.2k
Anne Pariser United States	17	229 0.4×	215 0.5×	137 1.3×	56 0.7×	60 0.8×	35	782
Gregory F. Guzauskas United States	16	223 0.4×	157 0.4×	103 1.0×	74 0.9×	75 0.9×	55	838
Saumya Shekhar Jamuar Singapore	15	335 0.5×	325 0.7×	16 0.1×	48 0.6×	69 0.9×	59	922
Anneliene Hechtelt Jonker France	13	256 0.4×	184 0.4×	83 0.8×	57 0.7×	41 0.5×	28	515

Countries citing papers authored by Annie Olry

Since Specialization

Citations

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

Fields of papers citing papers by Annie Olry

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annie Olry

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

1.

Weber, Stefanie, et al.. (2024). Coding undiagnosed rare disease patients in health information systems: recommendations from the RD-CODE project. Orphanet Journal of Rare Diseases. 19(1). 28–28. 3 indexed citations

2.

Chang, Willie, Pouria Mashouri, Alexander X. Lozano, et al.. (2020). Phenotate: crowdsourcing phenotype annotations as exercises in undergraduate classes. Genetics in Medicine. 22(8). 1391–1400.

3.

Wakap, Stéphanie Nguengang, Deborah M. Lambert, Annie Olry, et al.. (2019). Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database. European Journal of Human Genetics. 28(2). 165–173. 833 indexed citations breakdown →

4.

Olry, Annie, Marc Hanauer, Valérie Serrière-Lanneau, et al.. (2018). Harmonising phenomics information for a better interoperability in the rare disease field. European Journal of Medical Genetics. 61(11). 706–714. 16 indexed citations

5.

Rath, Ana, et al.. (2014). How to code rare diseases with international terminologies?. Orphanet Journal of Rare Diseases. 9(Suppl 1). O11–O11. 3 indexed citations

6.

Daniel, Marie Thérèse, et al.. (2014). Rare diseases and disabilities: improving the information available with three Orphanet projects. Orphanet Journal of Rare Diseases. 9(Suppl 1). O31–O31. 6 indexed citations

7.

Rath, Ana, et al.. (2012). Representation of rare diseases in health information systems: The orphanet approach to serve a wide range of end users. Human Mutation. 33(5). 803–808. 223 indexed citations

8.

Dhombres, Ferdinand, Pierre-Yves Vandenbussche, Ana Rath, et al.. (2011). OntoOrpha: An Ontology to Support Edition and Audit of Knowledge of Rare Diseases in ORPHANET.. 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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