Yves Lacassie

3.1k total citations
70 papers, 952 citations indexed

About

Yves Lacassie is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Yves Lacassie has authored 70 papers receiving a total of 952 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 23 papers in Molecular Biology and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Yves Lacassie's work include Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (12 papers) and Genomics and Rare Diseases (5 papers). Yves Lacassie is often cited by papers focused on Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (12 papers) and Genomics and Rare Diseases (5 papers). Yves Lacassie collaborates with scholars based in United States, Chile and Australia. Yves Lacassie's co-authors include Robin McGoey, Lisa G. Shaffer, Bryan D. Hall, Jill A. Rosenfeld, Jozef Gécz, James F. Gusella, Lawrence C. Layman, Lam Son Nguyen, Hyung‐Goo Kim and Yiping Shen and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Clinical Nutrition and Scientific Reports.

In The Last Decade

Yves Lacassie

65 papers receiving 907 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yves Lacassie United States 18 475 425 174 112 93 70 952
Andrew Norman United Kingdom 17 444 0.9× 211 0.5× 122 0.7× 55 0.5× 110 1.2× 30 825
Stavit A. Shalev Israel 19 519 1.1× 416 1.0× 107 0.6× 49 0.4× 108 1.2× 44 962
Guilherme Lopes Yamamoto Brazil 18 732 1.5× 469 1.1× 271 1.6× 98 0.9× 91 1.0× 57 1.3k
Melissa Lees United Kingdom 20 511 1.1× 673 1.6× 154 0.9× 68 0.6× 68 0.7× 37 1.1k
Louise Brueton United Kingdom 24 908 1.9× 604 1.4× 154 0.9× 76 0.7× 72 0.8× 34 1.5k
James V. Higgins United States 18 332 0.7× 414 1.0× 241 1.4× 57 0.5× 53 0.6× 39 927
Ann Haskins Olney United States 19 842 1.8× 716 1.7× 169 1.0× 48 0.4× 65 0.7× 43 1.4k
Jean‐Pierre Fryns Belgium 18 664 1.4× 635 1.5× 249 1.4× 44 0.4× 83 0.9× 72 1.3k
Nara Sobreira United States 19 690 1.5× 671 1.6× 113 0.6× 41 0.4× 86 0.9× 61 1.3k
L. A. Sandkuyl Netherlands 18 550 1.2× 297 0.7× 111 0.6× 40 0.4× 56 0.6× 29 1.1k

Countries citing papers authored by Yves Lacassie

Since Specialization
Citations

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

Fields of papers citing papers by Yves Lacassie

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yves Lacassie

This figure shows the co-authorship network connecting the top 25 collaborators of Yves Lacassie. A scholar is included among the top collaborators of Yves Lacassie 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 Yves Lacassie. Yves Lacassie 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.
Kishikawa, Shotaro, Vijay Gupta, Natalia T. Leach, et al.. (2023). A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome. Scientific Reports. 13(1). 12984–12984. 2 indexed citations
2.
Marble, Michael, et al.. (2020). Gorlin-like phenotype in a patient with a PTCH2 variant of uncertain significance. European Journal of Medical Genetics. 63(4). 103842–103842. 13 indexed citations
3.
Lacassie, Yves, Mahshid S. Azamian, Gladys Zapata, et al.. (2020). Vertical transmission of a large calvarial ossification defect due to heterozygous variants of ALX4 and TWIST1. American Journal of Medical Genetics Part A. 185(3). 916–922. 1 indexed citations
4.
Lacassie, Yves, Britt Johnson, Guillermo Lay‐Son, et al.. (2020). Severe SOPH syndrome due to a novel NBAS mutation in a 27‐year‐old woman—Review of this pleiotropic, autosomal recessive disorder: Mystery solved after two decades. American Journal of Medical Genetics Part A. 182(7). 1767–1775. 8 indexed citations
5.
León, Alejandro, et al.. (2017). New ocular finding in Baraitser-Winter syndrome (BWS). European Journal of Medical Genetics. 61(1). 21–23. 3 indexed citations
6.
Sahoo, Trilochan, Aaron Theisen, Pedro A. Sanchez‐Lara, et al.. (2011). Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate. American Journal of Medical Genetics Part A. 155(7). 1646–1653. 53 indexed citations
7.
Sathyamoorthi, Shyam, José D. Bermúdez, Mark Luquette, et al.. (2009). Array analysis and molecular studies of INI1 in an infant with deletion 22q13 (Phelan–McDermid syndrome) and atypical teratoid/rhabdoid tumor. American Journal of Medical Genetics Part A. 149A(5). 1067–1069. 10 indexed citations
8.
McGoey, Robin & Yves Lacassie. (2008). Adams–Oliver syndrome in siblings with central nervous system findings, epilepsy, and developmental delay: Refining the features of a severe autosomal recessive variant. American Journal of Medical Genetics Part A. 146A(4). 488–491. 29 indexed citations
9.
Collinsworth, Amy & Yves Lacassie. (2008). An unusual presentation of trisomy 13. American Journal of Medical Genetics Part A. 146A(11). 1490–1492. 1 indexed citations
10.
Lacassie, Yves, et al.. (2008). Is trisomy 14 mosaic a clinically recognizable syndrome?—Case report and review. American Journal of Medical Genetics Part A. 146A(12). 1609–1613. 19 indexed citations
11.
Anderson, Mary E., et al.. (2003). De novo paracentric inversion (X)(q26q28) with features mimicking Prader–Willi syndrome. American Journal of Medical Genetics Part A. 121A(1). 60–64. 6 indexed citations
12.
Lacassie, Yves, et al.. (1999). Ring 2 chromosome: Ten-year follow-up report. American Journal of Medical Genetics. 85(2). 117–122. 13 indexed citations
13.
Feingold, Murray, Bryan D. Hall, Yves Lacassie, & María‐Luisa Martínez‐Frías. (1997). Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay. American Journal of Medical Genetics. 69(3). 245–249. 37 indexed citations
14.
Feingold, Murray, et al.. (1997). Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay. American Journal of Medical Genetics. 69(3). 245–249. 1 indexed citations
15.
Clark, Robin D., et al.. (1989). Expanded phenotype and ethnicity in Setleis syndrome. American Journal of Medical Genetics. 34(3). 354–357. 22 indexed citations
16.
Cortés, Fanny, Yves Lacassie, F. Clarke Fraser, & M. Preus. (1986). An unusal case of ectodermal dysplasia. American Journal of Medical Genetics. 25(2). 289–291. 3 indexed citations
17.
Lacassie, Yves, et al.. (1981). [Secondary malnutrition: impact of genetic, metabolic and neurological involvement].. PubMed. 51(4). 257–60. 1 indexed citations
18.
Lacassie, Yves, et al.. (1980). Abstracts: 16th Annual Meeting Sociedad Latinoamericana de Investigacion Pediatrica. Pediatric Research. 14(1). 70–80. 1 indexed citations
19.
Lacassie, Yves, Richard A. Weinberg, & F Mönckeberg. (1978). Poor predictability of lactose malabsorption from clinical symptoms for Chilean populations. American Journal of Clinical Nutrition. 31(5). 799–804. 18 indexed citations
20.
Lacassie, Yves, et al.. (1977). Education and training of health professionals in genetics.. PubMed. 13(3B). 127–30.

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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