David Valle

39.8k total citations · 2 hit papers
226 papers, 14.4k citations indexed

About

David Valle is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, David Valle has authored 226 papers receiving a total of 14.4k indexed citations (citations by other indexed papers that have themselves been cited), including 149 papers in Molecular Biology, 57 papers in Clinical Biochemistry and 47 papers in Genetics. Recurrent topics in David Valle's work include Metabolism and Genetic Disorders (57 papers), Peroxisome Proliferator-Activated Receptors (40 papers) and Amino Acid Enzymes and Metabolism (24 papers). David Valle is often cited by papers focused on Metabolism and Genetic Disorders (57 papers), Peroxisome Proliferator-Activated Receptors (40 papers) and Amino Acid Enzymes and Metabolism (24 papers). David Valle collaborates with scholars based in United States, Canada and United Kingdom. David Valle's co-authors include Barton Childs, Albert-Ĺaszló Barabási, Michael E. Cusick, Marc Vidal, K.-I. Goh, Stephen J. Gould, Gary Steel, Hugo W. Moser, Gerardo Jiménez‐Sánchez and Ada Hamosh and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

David Valle

224 papers receiving 14.1k 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.

The human disease network

2007 2.3k citations K.-I. Goh, Michael E. Cusick et al. Proceedings of the National Academy of Sciences 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
David Valle United States	60	10.0k	2.7k	2.1k	1.6k	1.4k	226	14.4k
Hugo W. Moser United States	66	11.0k 1.1×	1.1k 0.4×	4.4k 2.1×	901 0.5×	4.0k 2.9×	275	14.4k
Giuseppe Attardi United States	77	18.5k 1.8×	1.6k 0.6×	5.5k 2.6×	961 0.6×	1.3k 1.0×	317	21.5k
Tomas A. Prolla United States	60	11.8k 1.2×	1.3k 0.5×	1.3k 0.6×	1.8k 1.1×	5.4k 3.9×	124	19.4k
Martin Hrabě de Angelis Germany	68	12.0k 1.2×	3.8k 1.4×	469 0.2×	1.4k 0.8×	3.8k 2.7×	485	21.3k
Ada Hamosh United States	39	7.1k 0.7×	4.8k 1.7×	727 0.4×	1.1k 0.7×	914 0.7×	99	13.3k
Stephen G. Young United States	96	14.1k 1.4×	1.8k 0.6×	607 0.3×	2.9k 1.8×	2.7k 1.9×	437	28.5k
David R. Thorburn Australia	65	13.3k 1.3×	1.4k 0.5×	7.0k 3.4×	697 0.4×	1.4k 1.0×	236	16.2k
Annemarie Poustka Germany	63	12.9k 1.3×	4.0k 1.4×	478 0.2×	1.4k 0.9×	1.4k 1.0×	230	18.0k
Mark A. Magnuson United States	95	16.1k 1.6×	6.4k 2.3×	454 0.2×	1.3k 0.8×	3.3k 2.4×	249	26.4k
Eric A. Schon United States	85	19.7k 2.0×	1.5k 0.5×	8.9k 4.3×	647 0.4×	3.1k 2.3×	221	23.5k

Countries citing papers authored by David Valle

Since Specialization

Citations

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

Fields of papers citing papers by David Valle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Valle

This figure shows the co-authorship network connecting the top 25 collaborators of David Valle. A scholar is included among the top collaborators of David Valle 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 David Valle. David Valle 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:

20 of 20 papers shown

Valle, David, et al.. (2023). A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2. Revista Paulista de Pediatria. 41. e2022057–e2022057. 2 indexed citations

Kratz, Lisa E., et al.. (2023). The remarkable journey of one female individual with ornithine transcarbamylase deficiency diagnosed post‐mortem. JIMD Reports. 64(3). 233–237. 1 indexed citations

Sobreira, Nara, Sean J. Griffith, Corina Antonescu, et al.. (2023). P669: VariantMatcher: A tool to enable connections amongst individuals with interest in a specific variant. SHILAP Revista de lepidopterología. 1(1). 100734–100734. 1 indexed citations

Martin, Renan Paulo, Elizabeth Wohler, Shaima Salman, et al.. (2022). Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome. PLoS Genetics. 18(12). e1010504–e1010504. 9 indexed citations

Han, Sangwoo T., et al.. (2022). A promoter variant in theOTCgene associated with late and variable age of onset hyperammonemia. Journal of Inherited Metabolic Disease. 45(4). 710–718. 4 indexed citations

Jelin, Angie C., Nara Sobreira, Elizabeth Wohler, et al.. (2020). The utility of exome sequencing for fetal pleural effusions. Prenatal Diagnosis. 40(5). 590–595. 10 indexed citations

Jurgens, Julie A., et al.. (2017). LMNA Sequences of 60,706 Unrelated Individuals Reveal 132 Novel Missense Variants in A-Type Lamins and Suggest a Link between Variant p.G602S and Type 2 Diabetes. Frontiers in Genetics. 8. 79–79. 15 indexed citations

Ben‐Salem, Salma, Nara L. M. Sobreira, Angeline M. Lyon, et al.. (2017). Defect in phosphoinositide signalling through a homozygous variant in PLCB3 causes a new form of spondylometaphyseal dysplasia with corneal dystrophy. Journal of Medical Genetics. 55(2). 122–130. 7 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

10.

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

11.

Goh, K.-I., Michael E. Cusick, David Valle, et al.. (2007). The human disease network. Proceedings of the National Academy of Sciences. 104(21). 8685–8690. 2301 indexed citations breakdown →

12.

Li, Xiaoling, Eveline Baumgart‐Vogt, James C. Morrell, et al.. (2002). PEX11α Is Required for Peroxisome Proliferation in Response to 4-Phenylbutyrate but Is Dispensable for Peroxisome Proliferator-Activated Receptor Alpha-Mediated Peroxisome Proliferation. Molecular and Cellular Biology. 22(23). 8226–8240. 129 indexed citations

13.

Baumgartner, Matthias R., Shlomo Almashanu, Terttu Suormala, et al.. (2001). The molecular basis of human 3-methylcrotonyl-CoA carboxylase deficiency. Journal of Clinical Investigation. 107(4). 495–504. 83 indexed citations

14.

Gaitán-Cepeda, Luis Alberto, et al.. (2000). Oral Lesions in HIV/AIDS Patients Undergoing Highly Active Antiretroviral Treatment Including Protease Inhibitors: A New Face of Oral AIDS?. AIDS Patient Care and STDs. 14(12). 627–635. 115 indexed citations

15.

Dodt, Gabriele, Nancy Braverman, David Valle, & Stephen J. Gould. (1996). From Expressed Sequence Tags to Peroxisome Biogenesis Disorder Genes. Annals of the New York Academy of Sciences. 804(1). 516–523. 16 indexed citations

16.

Sipilä, Ilkka, et al.. (1994). [Hyperornithinemia and gyrate atrophy: ornithine aminotransferase gene error causing a Finnish disease].. PubMed. 110(7). 681–6. 2 indexed citations

17.

Lemay, Jacinthe, Marie Lambert, Grant A. Mitchell, et al.. (1992). Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: Neurologic, ophthalmologic, and neuropsychologic examination of six patients. The Journal of Pediatrics. 121(5). 725–730. 25 indexed citations

18.

Bartholomew, Dennis W., Mark L. Batshaw, Robert H. Allen, et al.. (1988). Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuria. The Journal of Pediatrics. 112(1). 32–39. 55 indexed citations

19.

Mitchell, Grant A., Lawrence C. Brody, James E. Looney, et al.. (1988). An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.. Journal of Clinical Investigation. 81(2). 630–633. 77 indexed citations

20.

Antonarakis, Stylianos E., David Valle, Hugo W. Moser, et al.. (1984). Phenotypic variability in siblings with Farber disease. The Journal of Pediatrics. 104(3). 406–409. 39 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.

Explore authors with similar magnitude of impact