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Flora Tassone

Showing results (341-350 of 348) with videos related to

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American Journal of Human Genetics|August 8, 2020
Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with PhenotypeMichael S Breen, Paras Garg, Lara Tang, et al.
Cells|September 28, 2023
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on <i>FMR1</i> PremutationFlora Tassone, Dragana Protic, Emily Graves Allen, et al.
Circulation. Cardiovascular Genetics|October 14, 2017
Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the <i>GPR98</i> Locus on 5q14.3Tingwei Guo, Gabriela M Repetto, Donna M McDonald McGinn, et al.
American Journal of Human Genetics|December 25, 2019
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart DefectsYingjie Zhao, Alexander Diacou, H Richard Johnston, et al.
Nature Medicine|March 30, 2026
Deleterious coding variation associated with autism is shared across ancestriesMarina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.
Medrxiv : the Preprint Server for Health Sciences|January 20, 2025
Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populationsMarina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.
Nature Genetics|August 18, 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autismJack M Fu, F Kyle Satterstrom, Minshi Peng, et al.
Molecular Psychiatry|February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionIsabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Pageof 35

Showing results (341-350 of 348) with videos related to

Sort By:
Pageof 35
You have reached the last page of results.This site can display upto 348 results.
American Journal of Human Genetics|August 8, 2020
Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with PhenotypeMichael S Breen, Paras Garg, Lara Tang, et al.
Cells|September 28, 2023
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on <i>FMR1</i> PremutationFlora Tassone, Dragana Protic, Emily Graves Allen, et al.
Circulation. Cardiovascular Genetics|October 14, 2017
Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the <i>GPR98</i> Locus on 5q14.3Tingwei Guo, Gabriela M Repetto, Donna M McDonald McGinn, et al.
American Journal of Human Genetics|December 25, 2019
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart DefectsYingjie Zhao, Alexander Diacou, H Richard Johnston, et al.
Nature Medicine|March 30, 2026
Deleterious coding variation associated with autism is shared across ancestriesMarina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.
Medrxiv : the Preprint Server for Health Sciences|January 20, 2025
Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populationsMarina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.
Nature Genetics|August 18, 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autismJack M Fu, F Kyle Satterstrom, Minshi Peng, et al.
Molecular Psychiatry|February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionIsabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Pageof 35