François Schiettecatte

5.1k total citations · 2 hit papers
10 papers, 2.3k citations indexed

About

François Schiettecatte is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, François Schiettecatte has authored 10 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Cancer Research. Recurrent topics in François Schiettecatte's work include Genomics and Rare Diseases (8 papers), Cancer Genomics and Diagnostics (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). François Schiettecatte is often cited by papers focused on Genomics and Rare Diseases (8 papers), Cancer Genomics and Diagnostics (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). François Schiettecatte collaborates with scholars based in United States, Canada and United Kingdom. François Schiettecatte's co-authors include Ada Hamosh, Joanna Amberger, Carol Bocchini, Alan F. Scott, David Valle, Nara Sobreira, Corinne D. Boehm, Nara Sobreira, Julie Hoover‐Fong and V. Reid Sutton and has published in prestigious journals such as Nucleic Acids Research, Human Mutation and Genetics in Medicine.

In The Last Decade

François Schiettecatte

10 papers receiving 2.3k citations

Hit Papers

align trajectories sort by overperformance

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.

OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders

2014 1.6k citations Joanna Amberger, Carol Bocchini et al. Nucleic Acids Research profile →
GeneMatcher: A Matching Tool for Connecting Investigators with an Interest in the Same Gene

2015 449 citations Nara Sobreira, François Schiettecatte et al. Human Mutation profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
François Schiettecatte United States	7	1.4k	907	234	223	202	10	2.3k
Carol Bocchini United States	9	2.2k 1.6×	985 1.1×	308 1.3×	334 1.5×	386 1.9×	9	3.3k
Noam Nativ Israel	10	1.4k 1.0×	273 0.3×	373 1.6×	232 1.0×	241 1.2×	11	2.3k
Joanna Amberger United States	12	3.0k 2.2×	1.4k 1.5×	389 1.7×	481 2.2×	506 2.5×	18	4.7k
Isabelle Dussault United States	23	1.0k 0.7×	468 0.5×	181 0.8×	684 3.1×	73 0.4×	65	2.8k
Greg Stelzer United States	10	976 0.7×	194 0.2×	268 1.1×	199 0.9×	169 0.8×	20	2.0k
Seth Berger United States	18	1.2k 0.9×	214 0.2×	158 0.7×	168 0.8×	369 1.8×	44	1.8k
Mary Tagliaferri United States	25	735 0.5×	448 0.5×	175 0.7×	163 0.7×	54 0.3×	76	2.1k
Chi‐Wai Wong China	25	1.1k 0.8×	331 0.4×	324 1.4×	75 0.3×	48 0.2×	49	1.9k
Charlotte R. Williams United States	32	2.8k 2.0×	329 0.4×	462 2.0×	213 1.0×	31 0.2×	41	3.6k
Keith R. Stayrook United States	21	1.3k 0.9×	486 0.5×	180 0.8×	94 0.4×	55 0.3×	28	2.7k

Countries citing papers authored by François Schiettecatte

Since Specialization

Citations

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

Fields of papers citing papers by François Schiettecatte

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of François Schiettecatte

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

All Works

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10 of 10 papers shown

Applegate, Carolyn, François Schiettecatte, Ada Hamosh, & Joanna Amberger. (2022). Exploring Genes and Phenotypes Within Chromosomal Regions Using OMIM's GeneScout. Current Protocols. 2(9). e530–e530. 2 indexed citations

Sobreira, Nara, Harindra Arachchi, Orion J. Buske, et al.. (2017). Matchmaker Exchange. Current Protocols in Human Genetics. 95(1). 9.31.1–9.31.15. 32 indexed citations

Jurgens, Julie A., Hua Ling, Kurt N. Hetrick, et al.. (2015). Assessment of incidental findings in 232 whole-exome sequences from the Baylor–Hopkins Center for Mendelian Genomics. Genetics in Medicine. 17(10). 782–788. 35 indexed citations

Sobreira, Nara, François Schiettecatte, David Valle, & Ada Hamosh. (2015). GeneMatcher: A Matching Tool for Connecting Investigators with an Interest in the Same Gene. Human Mutation. 36(10). 928–930. 449 indexed citations breakdown →

Buske, Orion J., François Schiettecatte, Sergiu Dumitriu, et al.. (2015). The Matchmaker Exchange API: Automating Patient Matching Through the Exchange of Structured Phenotypic and Genotypic Profiles. Human Mutation. 36(10). 922–927. 35 indexed citations

Sobreira, Nara, François Schiettecatte, Corinne D. Boehm, David Valle, & Ada Hamosh. (2015). New Tools for Mendelian Disease Gene Identification: PhenoDB Variant Analysis Module; and GeneMatcher, a Web-Based Tool for Linking Investigators with an Interest in the Same Gene. Human Mutation. 36(4). 425–431. 78 indexed citations

Amberger, Joanna, Carol Bocchini, François Schiettecatte, Alan F. Scott, & Ada Hamosh. (2014). OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders. Nucleic Acids Research. 43(D1). D789–D798. 1646 indexed citations breakdown →

Hamosh, Ada, Nara Sobreira, Julie Hoover‐Fong, et al.. (2013). P heno DB : A New Web‐Based Tool for the Collection, Storage, and Analysis of Phenotypic Features. Human Mutation. 34(4). 566–571. 48 indexed citations

Schiettecatte, François. (1995). Document Retrieval Using The MPS Information Server (A Report on the TREC-6 Experiment).. Text REtrieval Conference. 315–326. 2 indexed citations

10.

Wright, Josephine A., et al.. (1990). The Genome Data Base (GDB). PubMed Central. 1056–1056. 1 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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