Paul Laissue

3.1k total citations
69 papers, 2.1k citations indexed

About

Paul Laissue is a scholar working on Molecular Biology, Public Health, Environmental and Occupational Health and Genetics. According to data from OpenAlex, Paul Laissue has authored 69 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 28 papers in Public Health, Environmental and Occupational Health and 27 papers in Genetics. Recurrent topics in Paul Laissue's work include Reproductive Biology and Fertility (24 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (15 papers) and Reproductive System and Pregnancy (10 papers). Paul Laissue is often cited by papers focused on Reproductive Biology and Fertility (24 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (15 papers) and Reproductive System and Pregnancy (10 papers). Paul Laissue collaborates with scholars based in Colombia, France and Australia. Paul Laissue's co-authors include Reiner A. Veitia, Liliana Catherine Patiño, Christine Bouchardy, Peter Schäfer, Georges Vlastos, Isabelle Neyroud‐Caspar, G Fioretta, André‐Pascal Sappino, Elisabetta Rapiti and John M. Kurtz and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Paul Laissue

66 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paul Laissue Colombia 23 742 724 585 413 364 69 2.1k
Ami Fishman Israel 27 409 0.6× 529 0.7× 411 0.7× 320 0.8× 1.1k 3.0× 121 2.5k
Julie Irving United Kingdom 28 794 1.1× 772 1.1× 260 0.4× 293 0.7× 1.1k 3.1× 66 2.8k
Mary Anne Rossing United States 22 379 0.5× 489 0.7× 617 1.1× 535 1.3× 848 2.3× 32 2.5k
Fredrika Pekonen Finland 30 319 0.4× 670 0.9× 426 0.7× 236 0.6× 545 1.5× 65 2.5k
Tatsuro Furui Japan 23 293 0.4× 986 1.4× 229 0.4× 156 0.4× 625 1.7× 110 2.1k
Nathalie Chabbert‐Buffet France 28 795 1.1× 252 0.3× 421 0.7× 182 0.4× 1.3k 3.6× 155 2.7k
H. A. Risch United States 11 278 0.4× 303 0.4× 280 0.5× 234 0.6× 647 1.8× 12 1.6k
Nilsa C. Ramirez United States 20 167 0.2× 802 1.1× 469 0.8× 615 1.5× 547 1.5× 45 2.4k
Joseph Menczer Israel 27 505 0.7× 435 0.6× 578 1.0× 236 0.6× 1.6k 4.4× 167 2.9k
Christopher J. McCabe United Kingdom 34 139 0.2× 848 1.2× 329 0.6× 475 1.2× 81 0.2× 90 3.0k

Countries citing papers authored by Paul Laissue

Since Specialization
Citations

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

Fields of papers citing papers by Paul Laissue

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paul Laissue

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

All Works

20 of 20 papers shown
1.
Oviedo, Juan Mauricio Pardo, et al.. (2021). A Pharmacogenetic Study of CYP2C19 in Acute Coronary Syndrome Patients of Colombian Origin Reveals New Polymorphisms Potentially Related to Clopidogrel Therapy. Journal of Personalized Medicine. 11(5). 400–400. 6 indexed citations
2.
Castro, Laura, et al.. (2021). Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies. International Journal of Molecular Sciences. 22(23). 12861–12861. 2 indexed citations
3.
Fonseca, Dora Janeth, et al.. (2021). Whole-Exome Sequencing in Patients Affected by Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Reveals New Variants Potentially Contributing to the Phenotype. Pharmacogenomics and Personalized Medicine. Volume 14. 287–299. 4 indexed citations
4.
Calderón‐Ospina, Carlos‐Alberto, et al.. (2020). Possible Genetic Determinants of Response to Phenytoin in a Group of Colombian Patients With Epilepsy. Frontiers in Pharmacology. 11. 555–555. 12 indexed citations
5.
Laissue, Paul, et al.. (2020). Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches. Reproductive Sciences. 27(8). 1541–1552. 20 indexed citations
6.
Laissue, Paul & Daniel Vaiman. (2020). Exploring the Molecular Aetiology of Preeclampsia by Massive Parallel Sequencing of DNA. Current Hypertension Reports. 22(4). 31–31. 6 indexed citations
7.
Fonseca, Dora Janeth, et al.. (2019). Mutant GNLY is linked to Stevens–Johnson syndrome and toxic epidermal necrolysis. Human Genetics. 138(11-12). 1267–1274. 6 indexed citations
8.
Restrepo, Carlos Martín, et al.. (2018). Creating and validating a warfarin pharmacogenetic dosing algorithm for Colombian patients. Pharmacogenomics and Personalized Medicine. Volume 11. 169–178. 12 indexed citations
9.
Restrepo, Carlos Martín, et al.. (2018). Identification of a New Candidate Locus for Ebstein Anomaly in 1p36.2. Molecular Syndromology. 9(3). 164–169. 5 indexed citations
10.
Amazit, Larbi, Liliana Catherine Patiño, F Magnin, et al.. (2018). ATG7 and ATG9A loss-of-function variants trigger autophagy impairment and ovarian failure. Genetics in Medicine. 21(4). 930–938. 68 indexed citations
11.
Mateus, Heidi, et al.. (2017). A first description of the Colombian national registry for rare diseases. BMC Research Notes. 10(1). 514–514. 13 indexed citations
12.
Laissue, Paul. (2015). Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing. Molecular and Cellular Endocrinology. 411. 243–257. 32 indexed citations
13.
Patiño, Liliana Catherine, et al.. (2014). Exome Sequencing Is an Efficient Tool for Variant Late-Infantile Neuronal Ceroid Lipofuscinosis Molecular Diagnosis. PLoS ONE. 9(10). e109576–e109576. 29 indexed citations
14.
Ortega‐Recalde, Oscar, Dora Janeth Fonseca, Liliana Catherine Patiño, et al.. (2013). A novel familial case of diffuse leukodystrophy related to NDUFV1 compound heterozygous mutations. Mitochondrion. 13(6). 749–754. 15 indexed citations
15.
Caburet, Sandrine, Petra Zavadáková, Ziva Ben‐Neriah, et al.. (2012). Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure. LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas).
16.
Laissue, Paul. (2011). Genómica funcional y medicina molecular del siglo XXI. LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas). 9(3). 217–218.
17.
L’Hôte, David, Paul Laissue, Catherine Serres, et al.. (2010). Interspecific resources: a major tool for quantitative trait locus cloning and speciation research. BioEssays. 32(2). 132–142. 14 indexed citations
18.
Laissue, Paul, Gaétan Burgio, David L’Hôte, et al.. (2009). Identification of Quantitative Trait Loci responsible for embryonic lethality in mice assessed by ultrasonography. The International Journal of Developmental Biology. 53(4). 623–629. 21 indexed citations
19.
Laissue, Paul, et al.. (2008). Analyse génétique des insuffisances ovariennes prématurées : implication des gènes forkhead et TGF-β. Gynécologie Obstétrique & Fertilité. 36(9). 862–871. 1 indexed citations
20.
Jeyabalan, Nallathambi, Paul Laissue, Frank Batista, et al.. (2008). Differential functional effects of novel mutations of the transcription factor FOXL2 in BPES patients. Human Mutation. 29(8). E123–E131. 22 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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