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Marsha M Wheeler

Showing results (11-20 of 35) with videos related to

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Journal of Cell Science|December 15, 2015
Activation of the IGF1 pathway mediates changes in cellular contractility and motility in single-suture craniosynostosisZeinab Al-Rekabi, Marsha M Wheeler, Andrea Leonard, et al.
Clinical Genetics|March 2, 2023
An FBN1 deep intronic variant is associated with pseudoexon formation and a variable Marfan phenotype in a five generation familyDong-Chuan Guo, Xueyan Duan, Kathleen Mimnagh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2018
Genomic characterization of the RH locus detects complex and novel structural variation in multi-ethnic cohortsMarsha M Wheeler, Kerry W Lannert, Haley Huston, et al.
Transfusion|November 24, 2020
Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed ProgramCarla L Dinardo, Theo G M Oliveira, Shannon Kelly, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 14, 2012
New meta-analysis tools reveal common transcriptional regulatory basis for multiple determinants of behaviorSeth A Ament, Charles A Blatti, Cedric Alaux, et al.
Communications Biology|June 10, 2024
Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparitiesEric Venner, Karynne Patterson, Divya Kalra, et al.
Medrxiv : the Preprint Server for Health Sciences|July 1, 2024
Frequency of pharmacogenomic variation and medication exposures among All of Us ParticipantsAndrew Haddad, Aparna Radhakrishnan, Sean McGee, et al.
Communications Biology|February 20, 2024
The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparitiesEric Venner, Karynne Patterson, Divya Kalra, et al.
The Journal of Experimental Medicine|March 16, 2021
Germline SAMD9L truncation variants trigger global translational repressionEric J Allenspach, Frank Soveg, Laura S Finn, et al.
Journal of Thrombosis and Haemostasis : JTH|January 28, 2020
Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome-wide analysis in African AmericansLaura M Raffield, Ake T Lu, Mindy D Szeto, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Journal of Cell Science|December 15, 2015
Activation of the IGF1 pathway mediates changes in cellular contractility and motility in single-suture craniosynostosisZeinab Al-Rekabi, Marsha M Wheeler, Andrea Leonard, et al.
Clinical Genetics|March 2, 2023
An FBN1 deep intronic variant is associated with pseudoexon formation and a variable Marfan phenotype in a five generation familyDong-Chuan Guo, Xueyan Duan, Kathleen Mimnagh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2018
Genomic characterization of the RH locus detects complex and novel structural variation in multi-ethnic cohortsMarsha M Wheeler, Kerry W Lannert, Haley Huston, et al.
Transfusion|November 24, 2020
Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed ProgramCarla L Dinardo, Theo G M Oliveira, Shannon Kelly, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 14, 2012
New meta-analysis tools reveal common transcriptional regulatory basis for multiple determinants of behaviorSeth A Ament, Charles A Blatti, Cedric Alaux, et al.
Communications Biology|June 10, 2024
Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparitiesEric Venner, Karynne Patterson, Divya Kalra, et al.
Medrxiv : the Preprint Server for Health Sciences|July 1, 2024
Frequency of pharmacogenomic variation and medication exposures among All of Us ParticipantsAndrew Haddad, Aparna Radhakrishnan, Sean McGee, et al.
Communications Biology|February 20, 2024
The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparitiesEric Venner, Karynne Patterson, Divya Kalra, et al.
The Journal of Experimental Medicine|March 16, 2021
Germline SAMD9L truncation variants trigger global translational repressionEric J Allenspach, Frank Soveg, Laura S Finn, et al.
Journal of Thrombosis and Haemostasis : JTH|January 28, 2020
Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome-wide analysis in African AmericansLaura M Raffield, Ake T Lu, Mindy D Szeto, et al.
Pageof 4