J L Blouin

804 total citations
13 papers, 490 citations indexed

About

J L Blouin is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, J L Blouin has authored 13 papers receiving a total of 490 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pediatrics, Perinatology and Child Health, 4 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in J L Blouin's work include Pain Management and Opioid Use (3 papers), Anesthesia and Pain Management (3 papers) and Prenatal Screening and Diagnostics (3 papers). J L Blouin is often cited by papers focused on Pain Management and Opioid Use (3 papers), Anesthesia and Pain Management (3 papers) and Prenatal Screening and Diagnostics (3 papers). J L Blouin collaborates with scholars based in United States, Switzerland and Italy. J L Blouin's co-authors include Stylianos E. Antonarakis, Ruth Landau, Richard M. Smiley, Dimitris Avramopoulos, Malachy O. Columb, Christian Kern, C. Conover Talbot, Constantinos Pángalos, George Thomas and Jacqueline Y. Maher and has published in prestigious journals such as Pain, Clinical Pharmacology & Therapeutics and Journal of Medical Genetics.

In The Last Decade

J L Blouin

13 papers receiving 474 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J L Blouin United States	11	236	197	138	130	110	13	490
Shane E. Brogan United States	12	131 0.6×	20 0.1×	87 0.6×	247 1.9×	176 1.6×	23	417
Emma J. Agnew United Kingdom	11	139 0.6×	14 0.1×	142 1.0×	6 0.0×	63 0.6×	13	357
Rachel L. Robinson United Kingdom	14	15 0.1×	79 0.4×	561 4.1×	39 0.3×	32 0.3×	20	668
Ágnes Nemeskéri Hungary	12	30 0.1×	25 0.1×	67 0.5×	16 0.1×	98 0.9×	39	397
Motoya Hashimoto Japan	6	155 0.7×	44 0.2×	154 1.1×	2 0.0×	55 0.5×	7	384
R. Brun del Re Canada	9	139 0.6×	26 0.1×	26 0.2×	8 0.1×	28 0.3×	16	452
Alexander Pearson Canada	7	166 0.7×	42 0.2×	195 1.4×	14 0.1×	16 0.1×	9	429
G Leboeuf Canada	16	61 0.3×	124 0.6×	156 1.1×	4 0.0×	94 0.9×	37	616
Larry R. Laufer United States	10	41 0.2×	237 1.2×	72 0.5×	4 0.0×	14 0.1×	13	751
Fawad Khan United States	10	63 0.3×	16 0.1×	62 0.4×	13 0.1×	16 0.1×	31	252

Countries citing papers authored by J L Blouin

Since Specialization

Citations

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

Fields of papers citing papers by J L Blouin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J L Blouin

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

All Works

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13 of 13 papers shown

Varvagiannis, Konstantinos, Sylviane Hanquinet, Peter C. Rimensberger, et al.. (2017). Congenital Neuronal Ceroid Lipofuscinosis with a Novel CTSD Gene Mutation: A Rare Cause of Neonatal-Onset Neurodegenerative Disorder. Neuropediatrics. 49(2). 150–153. 15 indexed citations

Fokstuen, Siv, Paola Melacini, Sabino Iliceto, et al.. (2011). Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice. Journal of Medical Genetics. 48(8). 572–576. 34 indexed citations

Camorcia, M., et al.. (2011). Effect of μ-opioid receptor A118G polymorphism on the ED50 of epidural sufentanil for labor analgesia. International Journal of Obstetric Anesthesia. 21(1). 40–44. 28 indexed citations

Sheth, Harsh, et al.. (2011). Triple-X Syndrome in a Trisomic Down Syndrome Child: Both Aneuploidies Originated from the Mother. International Journal of Human Genetics. 11(1). 51–53. 2 indexed citations

Wong, Cynthia A., Robert J. McCarthy, J L Blouin, & Ruth Landau. (2010). Observational study of the effect of μ-opioid receptor genetic polymorphism on intrathecal opioid labor analgesia and post-cesarean delivery analgesia. International Journal of Obstetric Anesthesia. 19(3). 246–253. 42 indexed citations

Landau, Ruth, Christian Kern, Malachy O. Columb, Richard M. Smiley, & J L Blouin. (2008). Genetic variability of the μ-opioid receptor influences intrathecal fentanyl analgesia requirements in laboring women ☆. Pain. 139(1). 5–14. 116 indexed citations

Landau, Ruth, et al.. (2005). Arg16 homozygosity of the β2-adrenergic receptor improves the outcome after β2-agonist tocolysis for preterm labor. Clinical Pharmacology & Therapeutics. 78(6). 656–663. 26 indexed citations

Radhakrishna, Uppala, et al.. (1997). Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis.. PubMed. 60(3). 597–604. 44 indexed citations

Pulver, Ann E., Paula Wolyniec, David E. Housman, et al.. (1996). . Cold Spring Harbor Symposia on Quantitative Biology. 61(1). 797–814. 12 indexed citations

10.

Blouin, J L, et al.. (1996). Mapping of the human holocarboxylase synthetase gene (HCS) to the Down syndrome critical region of chromosome 21q22.. PubMed. 39(3). 185–8. 6 indexed citations

11.

Antonarakis, Stylianos E., J L Blouin, Jacqueline Y. Maher, et al.. (1993). Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.. PubMed. 52(6). 1145–52. 85 indexed citations

12.

Gosset, Philippe, Didier Theophile, Martine Duterque‐Coquillaud, et al.. (1993). Mapping the Down Syndrome Chromosome Region. European Journal of Human Genetics. 1(1). 51–63. 24 indexed citations

13.

Blouin, J L, Dimitris Avramopoulos, Constantinos Pángalos, & Stylianos E. Antonarakis. (1993). Normal phenotype with paternal uniparental isodisomy for chromosome 21.. PubMed. 53(5). 1074–8. 56 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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