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Dragana Vuckovic

Showing results (1-10 of 58) with videos related to

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British Journal of Haematology|March 30, 2021
Advances in understanding the pathogenesis of hereditary macrothrombocytopeniaJanine Collins, William J Astle, Karyn Megy, et al.
Research and Practice in Thrombosis and Haemostasis|August 4, 2023
<i>PIK3R3</i> is a candidate regulator of platelet count in people of Bangladeshi ancestryKate Burley, Lucy Fitzgibbon, David van Heel, et al.
Bioinformatics (Oxford, England)|October 17, 2023
Automated calibration of consensus weighted distance-based clustering approaches using sharpBarbara Bodinier, Dragana Vuckovic, Sabrina Rodrigues, et al.
Plos One|January 24, 2014
Expression and replication studies to identify new candidate genes involved in normal hearing functionGiorgia Girotto, Dragana Vuckovic, Annalisa Buniello, et al.
Allergy|November 2, 2025
Trajectory-Based Clustering to Identify Asthma Subgroups Responsive to the Selective CXCR2 Antagonist, AZD5069Khezia Asamoah, Freda Yang, Ian M Adcock, et al.
Human Heredity|July 26, 2014
Consanguinity and hereditary hearing loss in QatarGiorgia Girotto, Massimo Mezzavilla, Khalid Abdulhadi, et al.
BMC Medical Genomics|August 13, 2015
Association of SNPs in LCP1 and CTIF with hearing in 11 year old children: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort and the G-EAR consortiumSean Harrison, Sarah J Lewis, Amanda J Hall, et al.
Communications Biology|October 26, 2023
Biological age estimation using circulating blood biomarkersJordan Bortz, Andrea Guariglia, Lucija Klaric, et al.
Pregnancy Hypertension|October 5, 2024
Association of genetic ancestry with pre-eclampsia in multi-ethnic cohorts of pregnant womenFrances Conti-Ramsden, Antonio de Marvao, Carolyn Gill, et al.
Plos One|December 7, 2013
Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing lossGiorgia Girotto, Khalid Abdulhadi, Annalisa Buniello, et al.
Pageof 6

Showing results (1-10 of 58) with videos related to

Sort By:
Pageof 6
British Journal of Haematology|March 30, 2021
Advances in understanding the pathogenesis of hereditary macrothrombocytopeniaJanine Collins, William J Astle, Karyn Megy, et al.
Research and Practice in Thrombosis and Haemostasis|August 4, 2023
<i>PIK3R3</i> is a candidate regulator of platelet count in people of Bangladeshi ancestryKate Burley, Lucy Fitzgibbon, David van Heel, et al.
Bioinformatics (Oxford, England)|October 17, 2023
Automated calibration of consensus weighted distance-based clustering approaches using sharpBarbara Bodinier, Dragana Vuckovic, Sabrina Rodrigues, et al.
Plos One|January 24, 2014
Expression and replication studies to identify new candidate genes involved in normal hearing functionGiorgia Girotto, Dragana Vuckovic, Annalisa Buniello, et al.
Allergy|November 2, 2025
Trajectory-Based Clustering to Identify Asthma Subgroups Responsive to the Selective CXCR2 Antagonist, AZD5069Khezia Asamoah, Freda Yang, Ian M Adcock, et al.
Human Heredity|July 26, 2014
Consanguinity and hereditary hearing loss in QatarGiorgia Girotto, Massimo Mezzavilla, Khalid Abdulhadi, et al.
BMC Medical Genomics|August 13, 2015
Association of SNPs in LCP1 and CTIF with hearing in 11 year old children: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort and the G-EAR consortiumSean Harrison, Sarah J Lewis, Amanda J Hall, et al.
Communications Biology|October 26, 2023
Biological age estimation using circulating blood biomarkersJordan Bortz, Andrea Guariglia, Lucija Klaric, et al.
Pregnancy Hypertension|October 5, 2024
Association of genetic ancestry with pre-eclampsia in multi-ethnic cohorts of pregnant womenFrances Conti-Ramsden, Antonio de Marvao, Carolyn Gill, et al.
Plos One|December 7, 2013
Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing lossGiorgia Girotto, Khalid Abdulhadi, Annalisa Buniello, et al.
Pageof 6