Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Denise M Kay

Showing results (41-50 of 73) with videos related to

Pageof 8
Sort By:
American Journal of Human Genetics|September 9, 2006
LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia agoCyrus P Zabetian, Carolyn M Hutter, Dora Yearout, et al.
BMC Medical Genetics|October 9, 2014
Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defectsFaith Pangilinan, Anne M Molloy, James L Mills, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 12, 2024
Characterization of 223 infants with CFTR-related metabolic syndrome/Cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID) identified during the first three years of newborn screening via IRT-DNA-SEQ in New York StateHossein Sadeghi, Denise M Kay, Elinor Langfelder-Schwind, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 15, 2018
Pilot study of population-based newborn screening for spinal muscular atrophy in New York stateJennifer N Kraszewski, Denise M Kay, Colleen F Stevens, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2020
Implementation of population-based newborn screening reveals low incidence of spinal muscular atrophyDenise M Kay, Colleen F Stevens, April Parker, et al.
Human Genetics|September 18, 2016
Copy-number variant analysis of classic heterotaxy highlights the importance of body patterning pathwaysErin M Hagen, Robert J Sicko, Denise M Kay, et al.
Pediatric Pulmonology|May 2, 2026
Evolution of the New York State Cystic Fibrosis Newborn Screening Algorithm: Two Decades of ExperienceElinor Langfelder-Schwind, Denise M Kay, Maria Berdella, et al.
Journal of Clinical Immunology|March 1, 2014
Newborn screening for SCID in New York State: experience from the first two yearsBeth H Vogel, Vincent Bonagura, Geoffrey A Weinberg, et al.
Neurology|July 14, 2022
Newborn Screening for Spinal Muscular Atrophy in New York State: Clinical Outcomes From the First 3 YearsBo Hoon Lee, Stella Deng, Claudia A Chiriboga, et al.
Nature Genetics|August 17, 2010
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's diseaseTaye H Hamza, Cyrus P Zabetian, Albert Tenesa, et al.
Pageof 8

Showing results (41-50 of 73) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|September 9, 2006
LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia agoCyrus P Zabetian, Carolyn M Hutter, Dora Yearout, et al.
BMC Medical Genetics|October 9, 2014
Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defectsFaith Pangilinan, Anne M Molloy, James L Mills, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 12, 2024
Characterization of 223 infants with CFTR-related metabolic syndrome/Cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID) identified during the first three years of newborn screening via IRT-DNA-SEQ in New York StateHossein Sadeghi, Denise M Kay, Elinor Langfelder-Schwind, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 15, 2018
Pilot study of population-based newborn screening for spinal muscular atrophy in New York stateJennifer N Kraszewski, Denise M Kay, Colleen F Stevens, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2020
Implementation of population-based newborn screening reveals low incidence of spinal muscular atrophyDenise M Kay, Colleen F Stevens, April Parker, et al.
Human Genetics|September 18, 2016
Copy-number variant analysis of classic heterotaxy highlights the importance of body patterning pathwaysErin M Hagen, Robert J Sicko, Denise M Kay, et al.
Pediatric Pulmonology|May 2, 2026
Evolution of the New York State Cystic Fibrosis Newborn Screening Algorithm: Two Decades of ExperienceElinor Langfelder-Schwind, Denise M Kay, Maria Berdella, et al.
Journal of Clinical Immunology|March 1, 2014
Newborn screening for SCID in New York State: experience from the first two yearsBeth H Vogel, Vincent Bonagura, Geoffrey A Weinberg, et al.
Neurology|July 14, 2022
Newborn Screening for Spinal Muscular Atrophy in New York State: Clinical Outcomes From the First 3 YearsBo Hoon Lee, Stella Deng, Claudia A Chiriboga, et al.
Nature Genetics|August 17, 2010
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's diseaseTaye H Hamza, Cyrus P Zabetian, Albert Tenesa, et al.
Pageof 8