Yves Lacassie

3.1k citations

70 papers · 952 indexed · h-index 18

Genetics top 5%
- Genomic variations and chromosomal abnormalities 17
- Genomics and Rare Diseases 5
- Genetic Syndromes and Imprinting 5
Developmental Biology top 10%
Neurology top 10%
Genetics
- Genomic variations and chromosomal abnormalities 17
- Genomics and Rare Diseases 5
- Genetic Syndromes and Imprinting 5
Molecular Biology
- Congenital heart defects research 5
- RNA modifications and cancer 5
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 12
Pathology and Forensic Medicine
- Tumors and Oncological Cases 5
Pulmonary and Respiratory Medicine
- Tracheal and airway disorders 4

Co-authors: Robin McGoey Lisa G. Shaffer Bryan D. Hall Jill A. Rosenfeld Yiping Shen James F. Gusella Hyung‐Goo Kim Lam Son Nguyen
Cited by: Genetics Developmental Biology Neurology
Journals: European Journal of Medical Genetics (5 papers)American Journal of Medical Genetics Part A (19 papers)Journal of Pediatric Orthopaedics (2 papers)
Partner nations: United States Chile Australia

In The Last Decade

Yves Lacassie

65 papers receiving 907 citations

Peers

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

The 25 scholars most cited alongside Yves Lacassie, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Yves Lacassie Line = papers co-authored together Yves Lacassie links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	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 ·So Yuncho,Shotaro Kishikawa,Vijay Gupta,Natalia T. Leach,Yiping Shen,Oana Moldovan,Himanshu Goel,N. Balambigai,D Manikanta,Nicolas Gruchy,Saskia M. Maas,Yves Lacassie,Soo‐Hyun Kim,Woo-Yang Kim,Bradley J. Quade,Cynthia C. Morton,Cheol‐Hee Kim,Lawrence C. Layman,Hyung‐Goo Kim	2023	2
2	Vertical transmission of a large calvarial ossification defect due to heterozygous variants of ALX4 and TWIST1 American Journal of Medical Genetics Part A ·A. D. Muhammad,Yves Lacassie,Mahshid S. Azamian,Masasumi Akahoshi,Gladys Zapata,Patricia Hernandez,Pengfei Liu,Ian M. Campbell,Bret L. Bostwick,Seema R. Lalani	2020	1
3	Gorlin-like phenotype in a patient with a PTCH2 variant of uncertain significance European Journal of Medical Genetics ·褚军,Andrea Winokur Kotula,Kuan-Jen Huang,Michael Marble,J. Noordegraaf,Yves Lacassie	2020	13
4	New ocular finding in Baraitser-Winter syndrome (BWS) European Journal of Medical Genetics ·L Minkin,Alejandro León,Ricardo Gómez,Ana Maria Jula,Yves Lacassie	2017	3
5	Familial co-segregation of Coffin–Lowry syndrome inherited from the mother and autosomal dominant Waardenburg type IV syndrome due to deletion of EDNRB inherited from the father European Journal of Medical Genetics ·Jacob M. Loupe,Srirangan Sampath,Yves Lacassie	2014	3
6	Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders Human Molecular Genetics ·Lam Son Nguyen,Hyung‐Goo Kim,Jill A. Rosenfeld,Yiping Shen,James F. Gusella,Yves Lacassie,Lawrence C. Layman,Lisa G. Shaffer,Jozef Gécz	2013	116
7	Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate American Journal of Medical Genetics Part A ·Trilochan Sahoo,Aaron Theisen,Pedro A. Sanchez‐Lara,Michael Marble,كریم محمد ابراهیم محمد عطیة عطیة,Beth S. Torchia,Allen N. Lamb,Bassem A. Bejjani,Lisa G. Shaffer,Yves Lacassie	2011	53
8	Serendipitous diagnosis of mild recessive multiple epiphyseal dysplasia through parental‐targeted screening test American Journal of Medical Genetics Part A ·Yves Lacassie,John Storment,Gabriel A. Lazarin	2011	2
9	New cases and refinement of the critical region in the 1q41q42 microdeletion syndrome European Journal of Medical Genetics ·Jill A. Rosenfeld,Yves Lacassie,Dima El‐Khechen,Luis Escobar,James D. Reggin,Lismanto Y. Tuluki,Emily Chen,Lauren S. Jenkins,Noah Crooks,Samuel H. Zinner,Melanie Babcock,Bernice E. Morrow,Roger A. Schultz,Beth S. Torchia,Blake C. Ballif,Karen D. Tsuchiya,Lisa G. Shaffer	2010	27
10	Siblings with phenotypic overlap with Toriello–Carey syndrome and complex cytogenetic imbalances including 3q29 microduplication and 6p25 microdeletion: Review of the literature and additional evidence for genetic heterogeneity American Journal of Medical Genetics Part A ·Robin McGoey,P Sathishkannan,Yves Lacassie	2010	8
11	Paternal balanced reciprocal translocation t(9;22)(q34.3;q11.2) resulting in an lnfant with features of the 9q subtelomere and the 22q11 deletion syndromes due to 3:1 meiotic segregation and tertiary monosomy American Journal of Medical Genetics Part A ·Robin McGoey,Yves Lacassie	2009	20
12	Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effects European Journal of Human Genetics ·Vinciane Wouters,Nisha Limaye,Mélanie Uebelhoer,Alexandre Irrthum,Laurence M. Boon,John B. Mulliken,O Enjolras,Eulàlia Baselga,Jonathan Berg,A. Dompmartin,Sten A. Ivarsson,Loshan Kangesu,Yves Lacassie,Jill Murphy,Ahmad S. Teebi,Anthony Penington,Paul N.M.A. Rieu,Miikka Vikkula	2009	111
13	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 ·Shyam Sathyamoorthi,Marta Elviani,José D. Bermúdez,Rosnanda Sukmawati,Mark Luquette,Robin McGoey,க. மகாராஜன்,Jhoanny Rasojivola,Jaclyn A. Biegel,Yves Lacassie	2009	10
14	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 ·Robin McGoey,Yves Lacassie	2008	29
15	De novo paracentric inversion (X)(q26q28) with features mimicking Prader–Willi syndrome American Journal of Medical Genetics Part A ·春藤恭昌,Mary E. Anderson,Yves Lacassie	2003	6
16	Ring 2 chromosome: Ten-year follow-up report American Journal of Medical Genetics ·Yves Lacassie,Eun-Jeong 임은정Lim,Alfonso Vargas,Mengxin Ren	1999	13
17	Satoyoshi syndrome: An unusual postnatal multisystemic disorder American Journal of Medical Genetics ·Mohammad Ehlayel,Yves Lacassie	1995	17
18	Expanded phenotype and ethnicity in Setleis syndrome American Journal of Medical Genetics ·Robin D. Clark,Mahin Golabi,Yves Lacassie,Bryan D. Hall,Ngozi Jacinta Ozoh	1989	22
19	Abstracts: 16th Annual Meeting Sociedad Latinoamericana de Investigacion Pediatrica Pediatric Research ·Infants Chavez,Бутенко Е.В.,Susanne Mönch,Yves Lacassie,Kristel Van den Broeck,B. V. Robinson,Ignacio Araya,Diogo Cesar M. de Oliveira Jatobá,Aron J. Diament,行木敬,D S Basavaraju,豊一吉岡,(unknown),(unknown),(unknown),(unknown)	1980	1
20	Poor predictability of lactose malabsorption from clinical symptoms for Chilean populations American Journal of Clinical Nutrition ·Yves Lacassie,Richard A. Weinberg,F Mönckeberg	1978	18

About Yves Lacassie

Yves Lacassie is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 70 papers that have together received 952 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (12 papers), Genomics and Rare Diseases (5 papers), Genetic Syndromes and Imprinting (5 papers), Congenital heart defects research (5 papers), RNA modifications and cancer (5 papers), Tumors and Oncological Cases (5 papers) and Tracheal and airway disorders (4 papers). The work is most often cited by research in Genetics (425 citations), Developmental Biology (29 citations) and Neurology (112 citations). Yves Lacassie has collaborated with scholars based in United States, Chile and Australia. Frequent co-authors include Robin McGoey, Lisa G. Shaffer, Bryan D. Hall, Jill A. Rosenfeld, Yiping Shen, James F. Gusella, Hyung‐Goo Kim, Lam Son Nguyen, Lawrence C. Layman and Jozef Gécz. Their work appears in journals such as European Journal of Medical Genetics, American Journal of Medical Genetics Part A, Journal of Pediatric Orthopaedics, Pediatric Research and Journal of Child Neurology.

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