Faculty

Institution

Unit

Venue

Yves Lacassie

Louisiana State University Health Sciences Center, New Orleans

Affiliations

Cytogenetics Laboratory

Departments Of Microbiology And Immunology, Genetics And Medicine

Louisiana State University Health Sciences Center, New Orleans

NoneYves Lacassie is currently serving as a Cytogenetics Laboratory faculty at Louisiana State University Health Sciences Center, New Orleans.

Honors

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Experiences

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Education

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Yves Lacassie

Louisiana State University Health Sciences Center, New Orleans

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genetics human genetics genetic disorders medical genetics pathology mendelian disorder molecular genetics developmental anomalies genomics developmental biology neurogenetics neuropathology heredity anatomical pathology disease gene identification molecular medicine genome biology pediatrics cytogenetics child neurology craniofacial research scleroderma developmental genetics reproductive biology neurodevelopmental disorders histopathology molecular diagnostics mutagenesis developmental delay musculoskeletal disorders reproductive medicine reproductive science intellectual disability surgical pathology forensic genetics chromosome biology chromosomal rearrangements genetic factors psychiatric genetics andrology variant interpretation preterm birth allelic variant genetic testing inborn errors of immunity immunologic diseases microdeletion syndrome satoyoshi syndrome mental retardation craniofacial surgery developmental system genome studies genome analysis vascular malformations cleft lip applied genetics mendelian inheritance abnormal development developmental disabilities disease susceptibility steroid metabolism global developmental delay disease mechanisms parathyroid glands severe developmental delay two-hit model human congenital anomalies balanced cytogenetic abnormalities genomic landscape copy number variants neuro-developmental disorders magi2 gene variable epilepsy cleft palate meiotic segregation deletion syndromes

Notable Scholarly Works

Notable Federal Grants

Collaborators

Impact of Genetic and Non-Genetic Factors on Phenotypic Diversity in Nbas-Associated Disease. Molecular Genetics and Metabolism (2024)

Nicole HammannDominic LenzIvo BaricEllen CrushellCarlo Dionisi ViciFelix DistelmaierFrancois FeilletPeter FreisingerMaja HempelAnna L. KhorevaMartin W. LaassYves LacassieElke LainkaCatherine Larson-NathZhongdie LiPatryk LipińskiEberhard LurzAndré MégarbanéSusana NobreGiorgia OlivieriBianca PetersPaolo PronteraLea D. SchliebenChristine M. SeroogyCristina SobacchiShigeru SuzukiChristel TranJerry VockleyJian-She WangMatias WagnerHolger ProkischSven F. GarbadeStefan KölkerGeorg F. HoffmannChristian Staufner

genomicsnbas-associated diseasegenetic factorsphenotypic diversitygeneticsbiologymolecular geneticsmolecular biologynon-genetic factorshuman geneticsgenotype-phenotype association

Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of Pgap2 Variants in Hyperphosphatasia With Impaired Intellectual Development Syndrome 3 (Hpmrs3). Human Mutation (2024)

Seda SusgunAfif Ben-MahmoudFranz RüschendorfBonsu KuSyeda Iqra HussainSolveig SchulzOliver PukSaskia BiskupJonathan D. J. LabonneDilan Wellalage DonVijay GuptaTae-Ik ChoiSaadullah KhanNaveed WasifYves LacassieLawrence C. LaymanSibel Aylin Ugur IseriCheol-Hee KimHyung-Goo Kim

genomicsphenotypic spectrummutagenesisgeneticsgenetic variationmolecular biologyhuman geneticsgenetic disordersdigital anomalies

Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of Cnksr2 in the Houge Type of X‐Linked Syndromic Intellectual Development Disorder ( Mrxshg ). American Journal of Medical Genetics Part A (2024)

Mohammad‐Reza GhasemiSahand Tehrani FatehAfif Ben‐MahmoudVijay GuptaLara G. StühnGaetan LescaNicolas ChatronKonrad PlatzerPatrick EderyHossein SadeghiBertrand IsidorBenjamin CognéHeidi L. SchulzIlona Krauspe‐StübeckeRadhakrishnan PeriyasamySheela NampoothiriReza MirfakhraieSahar AlijanpourSteffen SyrbeUlrich PfeiferStephanie SprangerKathrin Grundmann‐HauserTobias B. HaackMaria T. PapadopoulouTayrine da Silva GonçalvesEleni PanagiotakakiAlexis ArzimanoglouSeyed Hassan TonekaboniMassimiliano RossiG. Christoph KorenkeYves LacassieMi‐Hyeon JangLawrence C. LaymanMohammad MiryounesiHyung‐Goo Kim

neurologynovel digital anomaliesphenotypic spectraneurogeneticsgeneticsneurodevelopmental disordersdevelopmental disordershippocampal atrophyneuroscience

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 (2023)

Afif Ben-MahmoudShotaro KishikawaVijay GuptaNatalia T. LeachYiping ShenOana MoldovanHimanshu GoelBruce HopperKara RanguinNicolas GruchySaskia M MaasYves LacassieSoo-Hyun KimWoo-Yang KimBradley J. QuadeCynthia C. MortonCheol-Hee KimLawrence C. LaymanHyung-Goo Kim

intellectual disabilityhuman geneticsgeneticshla typing

Biallelic Variants in Wars1 Cause a Highly Variable Neurodevelopmental Syndrome and Implicate a Critical Exon for Normal Auditory Function. Human Mutation (2022)

Sheng‐Jia LinBarbara VonaHillary M. PorterMahmoud IzadiKevin HuangYves LacassieJill A. RosenfeldSaadullah KhanCassidy PetreeTayyiba A. AliNazif MuhammadSher A. KhanNoor MuhammadPengfei LiuMarie‐Louise HaymonFranz RüschendorfIl‐Keun KongLinda SchnappNatasha ShurLynn ChorichLawrence LaymanThomas HaafEhsan PourkarimiHyung‐Goo KimGaurav K. Varshney

critical exonneurogeneticsbiallelic variantsgeneticsgenetic variationmolecular biologyinfectious diseaseshuman geneticspopulation genetics

Front Cover, Volume 43, Issue 10. Human Mutation (2022)

human geneticsgeneticsfront cover

Mild Ocular Findings and Skeletal Anomalies Producing a Marfanoid Appearance, Along With Autoimmune/Inflammatory Findings Due to Snv of Unknown Significance in Genes Abcc6 and Opa1 Inherited From the Mother. World Journal of Ophthalmology & Vision Research (2022)

pathogenesisophthalmologyautoimmune diseasesneuro-ophthalmologyanatomical pathologydevelopmental anomaliesmarfanoid appearancegeneticsmendelian disorderskeletal anomaliesmolecular geneticsopa1 inheritedmedical geneticspathologyhuman geneticsgenetic disorders

Clinical and Molecular Features of 66 Patients With Musculocontractural Ehlers−Danlos Syndrome Caused by Pathogenic Variants in Chst14 (Mceds- Chst14 ). Journal of Medical Genetics (2021)

pathogenic variantsautoimmune diseasesmolecular featuresmendelian disorderinborn errors of immunitymusculoskeletal disorderspathologyhuman geneticsarthritismedicineimmunologic diseasesmusculocontractural ehlers−danlos syndromedisease gene identificationdisease susceptibilityrheumatismsclerodermamyositisclinical rheumatologymolecular medicine

Lessons From a 30 Year Follow‐Up of Monozygotic Twins With Discordant Phenotype Due to a Ring 13 Chromosomal Mosaicism in One of Them. American Journal of Medical Genetics Part A (2021)

forensic geneticsdiscordant phenotypegenetic recombinationhereditymonozygotic twinsgeneticsdevelopmental biologymedical geneticshuman geneticsgenetic disorderschromosomal mosaicism

Further Delineation of Basel‐Vanagaite‐Smirin‐Yosef Syndrome: Report of Three Patients. American Journal of Medical Genetics Part A (2020)

medicineinternal medicineneurological disorderssystemic sclerodermadiagnosisneuropathologyworld psychiatrysclerodermatranslational psychiatrychild neurologyfurther delineation

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Yves Lacassie

Louisiana State University Health Sciences Center, New Orleans

Affiliations

Cytogenetics Laboratory

Departments Of Microbiology And Immunology, Genetics And Medicine

Louisiana State University Health Sciences Center, New Orleans

NoneYves Lacassie is currently serving as a Cytogenetics Laboratory faculty at Louisiana State University Health Sciences Center, New Orleans.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Yves Lacassie

Louisiana State University Health Sciences Center, New Orleans

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Impact of Genetic and Non-Genetic Factors on Phenotypic Diversity in Nbas-Associated Disease. Molecular Genetics and Metabolism (2024)

genomicsnbas-associated diseasegenetic factorsphenotypic diversitygeneticsbiologymolecular geneticsmolecular biologynon-genetic factorshuman geneticsgenotype-phenotype association

Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of Pgap2 Variants in Hyperphosphatasia With Impaired Intellectual Development Syndrome 3 (Hpmrs3). Human Mutation (2024)

genomicsphenotypic spectrummutagenesisgeneticsgenetic variationmolecular biologyhuman geneticsgenetic disordersdigital anomalies

neurologynovel digital anomaliesphenotypic spectraneurogeneticsgeneticsneurodevelopmental disordersdevelopmental disordershippocampal atrophyneuroscience

intellectual disabilityhuman geneticsgeneticshla typing

Biallelic Variants in Wars1 Cause a Highly Variable Neurodevelopmental Syndrome and Implicate a Critical Exon for Normal Auditory Function. Human Mutation (2022)

critical exonneurogeneticsbiallelic variantsgeneticsgenetic variationmolecular biologyinfectious diseaseshuman geneticspopulation genetics

Front Cover, Volume 43, Issue 10. Human Mutation (2022)

human geneticsgeneticsfront cover

Clinical and Molecular Features of 66 Patients With Musculocontractural Ehlers−Danlos Syndrome Caused by Pathogenic Variants in Chst14 (Mceds- Chst14 ). Journal of Medical Genetics (2021)

Lessons From a 30 Year Follow‐Up of Monozygotic Twins With Discordant Phenotype Due to a Ring 13 Chromosomal Mosaicism in One of Them. American Journal of Medical Genetics Part A (2021)

forensic geneticsdiscordant phenotypegenetic recombinationhereditymonozygotic twinsgeneticsdevelopmental biologymedical geneticshuman geneticsgenetic disorderschromosomal mosaicism

Further Delineation of Basel‐Vanagaite‐Smirin‐Yosef Syndrome: Report of Three Patients. American Journal of Medical Genetics Part A (2020)

medicineinternal medicineneurological disorderssystemic sclerodermadiagnosisneuropathologyworld psychiatrysclerodermatranslational psychiatrychild neurologyfurther delineation

1
2
3
4
5
9
10 / page