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J Collin

Showing results (301-310 of 449) with videos related to

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The Annals of Otology, Rhinology, and Laryngology|June 15, 2007
Phenotype description of a novel DFNA9/COCH mutation, I109TRobert J Pauw, Patrick L M Huygen, Rob W J Collin, et al.
Epidemiology (Cambridge, Mass.)|December 16, 2020
Estimating the Unknown: Greater Racial and Ethnic Disparities in COVID-19 Burden After Accounting for Missing Race and Ethnicity DataKatie Labgold, Sarah Hamid, Sarita Shah, et al.
Medrxiv : the Preprint Server for Health Sciences|October 7, 2020
Measuring the missing: greater racial and ethnic disparities in COVID-19 burden after accounting for missing race/ethnicity dataKatie Labgold, Sarah Hamid, Sarita Shah, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|July 31, 2024
Sociodemographic and Socioeconomic Factors Correlate with Late-Stage Pediatric Hodgkin Lymphoma and Rhabdomyosarcoma: A Report from the Children's Oncology Group RegistriesJudy Y Ou, Heydon K Kaddas, Todd A Alonzo, et al.
Molecular Vision|October 19, 2012
Identification of a novel nonsense mutation in RP1 that causes autosomal recessive retinitis pigmentosa in an Indonesian familyAnna M Siemiatkowska, Galuh D N Astuti, Kentar Arimadyo, et al.
International Journal of Molecular Sciences|March 10, 2018
Antisense Oligonucleotide-Based Splicing Correction in Individuals with Leber Congenital Amaurosis due to Compound Heterozygosity for the c.2991+1655A>G Mutation in CEP290Lonneke Duijkers, L Ingeborgh van den Born, John Neidhardt, et al.
Investigative Ophthalmology & Visual Science|March 23, 2011
Autosomal recessive Stickler syndrome in two families is caused by mutations in the COL9A1 geneKonstantinos Nikopoulos, Isabelle Schrauwen, Marleen Simon, et al.
NPJ Breast Cancer|May 30, 2026
Neighborhood deprivation and oncotype DX recurrence scores among Black and White women: the interplay between race, place, and tumor biologyJasmine M Miller-Kleinhenz, Lauren E Barber, Maret L Maliniak, et al.
Stem Cell Research|February 5, 2022
Generation of a patient-derived induced pluripotent cell line (SCTCi016-A) carrying a homozygous variant in RPE65Irene Vázquez-Domínguez, Michael Kwint, Hester Y Kroes, et al.
American Journal of Epidemiology|July 9, 2020
Bayesian Pathway Analysis for Complex InteractionsJames W Baurley, Anders Kjærsgaard, Michael E Zwick, et al.
Pageof 45

Showing results (301-310 of 449) with videos related to

Sort By:
Pageof 45
The Annals of Otology, Rhinology, and Laryngology|June 15, 2007
Phenotype description of a novel DFNA9/COCH mutation, I109TRobert J Pauw, Patrick L M Huygen, Rob W J Collin, et al.
Epidemiology (Cambridge, Mass.)|December 16, 2020
Estimating the Unknown: Greater Racial and Ethnic Disparities in COVID-19 Burden After Accounting for Missing Race and Ethnicity DataKatie Labgold, Sarah Hamid, Sarita Shah, et al.
Medrxiv : the Preprint Server for Health Sciences|October 7, 2020
Measuring the missing: greater racial and ethnic disparities in COVID-19 burden after accounting for missing race/ethnicity dataKatie Labgold, Sarah Hamid, Sarita Shah, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|July 31, 2024
Sociodemographic and Socioeconomic Factors Correlate with Late-Stage Pediatric Hodgkin Lymphoma and Rhabdomyosarcoma: A Report from the Children's Oncology Group RegistriesJudy Y Ou, Heydon K Kaddas, Todd A Alonzo, et al.
Molecular Vision|October 19, 2012
Identification of a novel nonsense mutation in RP1 that causes autosomal recessive retinitis pigmentosa in an Indonesian familyAnna M Siemiatkowska, Galuh D N Astuti, Kentar Arimadyo, et al.
International Journal of Molecular Sciences|March 10, 2018
Antisense Oligonucleotide-Based Splicing Correction in Individuals with Leber Congenital Amaurosis due to Compound Heterozygosity for the c.2991+1655A>G Mutation in CEP290Lonneke Duijkers, L Ingeborgh van den Born, John Neidhardt, et al.
Investigative Ophthalmology & Visual Science|March 23, 2011
Autosomal recessive Stickler syndrome in two families is caused by mutations in the COL9A1 geneKonstantinos Nikopoulos, Isabelle Schrauwen, Marleen Simon, et al.
NPJ Breast Cancer|May 30, 2026
Neighborhood deprivation and oncotype DX recurrence scores among Black and White women: the interplay between race, place, and tumor biologyJasmine M Miller-Kleinhenz, Lauren E Barber, Maret L Maliniak, et al.
Stem Cell Research|February 5, 2022
Generation of a patient-derived induced pluripotent cell line (SCTCi016-A) carrying a homozygous variant in RPE65Irene Vázquez-Domínguez, Michael Kwint, Hester Y Kroes, et al.
American Journal of Epidemiology|July 9, 2020
Bayesian Pathway Analysis for Complex InteractionsJames W Baurley, Anders Kjærsgaard, Michael E Zwick, et al.
Pageof 45