Anna Morgan
Anna Morgan
University of Trieste
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Rare and low-frequency coding variants alter human adult height
E Marouli, M Graff, C Medina-Gomez, KS Lo, AR Wood, TR Kjaer, RS Fine, ...
Nature 542 (7640), 186-190, 2017
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
HR Warren, E Evangelou, CP Cabrera, H Gao, M Ren, B Mifsud, I Ntalla, ...
Nature genetics 49 (3), 403, 2017
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
E Evangelou, HR Warren, D Mosen-Ansorena, B Mifsud, R Pazoki, H Gao, ...
Nature genetics 50 (10), 1412, 2018
Novel blood pressure locus and gene discovery using genome-wide association study and expression data sets from blood and the kidney
LV Wain, A Vaez, R Jansen, R Joehanes, PJ van der Most, ...
Hypertension, HYPERTENSIONAHA. 117.09438, 2017
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients
D Vozzi, A Morgan, D Vuckovic, A D'Eustacchio, K Abdulhadi, E Rubinato, ...
Gene 542 (2), 209-216, 2014
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta
E Rubinato, A Morgan, A D'Eustacchio, V Pecile, G Gortani, P Gasparini, ...
Gene 545 (2), 290-292, 2014
Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection
E Athanasakis, D Licastro, F Faletra, A Fabretto, S Dipresa, D Vozzi, ...
American Journal of Medical Genetics Part A 164 (1), 170-176, 2014
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss
F Faletra, G Girotto, AP D'Adamo, D Vozzi, A Morgan, P Gasparini
Gene 534 (2), 236-239, 2014
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis
GG S Lenarduzzi, D Vozzi, A Morgan, E Rubinato, A D'Eustacchio, TM Osland, C ...
Hearing research 320, 18-23, 2015
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss
D Vuckovic, S Dawson, DI Scheffer, T Rantanen, A Morgan, M Di Stazio, ...
Human molecular genetics 24 (19), 5655-5664, 2015
Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort
F Faletra, E Athanasakis, A Morgan, X Biarnés, F Fornasier, R Parini, ...
Gene 521 (1), 160-165, 2013
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families
MK Alkowari, D Vozzi, S Bhagat, N Krishnamoorthy, A Morgan, Y Hayder, ...
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 800, 29-36, 2017
The p. Cys169Tyr variant of connexin 26 is not a polymorphism
F Zonta, G Girotto, D Buratto, G Crispino, A Morgan, K Abdulhadi, ...
Human molecular genetics 24 (9), 2641-2648, 2015
A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways
T Agnew, M Goldsworthy, C Aguilar, A Morgan, M Simon, H Hilton, ...
Cell reports 25 (12), 3315-3328. e6, 2018
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss
A Morgan, D Vuckovic, N Krishnamoorthy, E Rubinato, U Ambrosetti, ...
European Journal of Human Genetics, 1, 2018
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection
D Vuckovic, M Mezzavilla, M Cocca, A Morgan, M Brumat, E Catamo, ...
European Journal of Human Genetics, 1, 2018
TBL1Y: a new gene involved in syndromic hearing loss
M Di Stazio, C Collesi, D Vozzi, W Liu, M Myers, A Morgan, PA D Adamo, ...
European journal of human genetics: EJHG, 2018
Genetic analysis of over one million people identifies 535 novel loci for blood pressure.
E Evangelou, HR Warren, D Mosen-Ansorena, B Mifsud, R Pazoki, H Gao, ...
bioRxiv, 198234, 2017
Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability
A Morgan, I Gandin, C Belcaro, P Palumbo, O Palumbo, E Biamino, ...
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 781, 32-36, 2015
Assessment of the Olfactory Function in Italian Patients with Type 3 von Willebrand Disease Caused by a Homozygous 253 Kb Deletion Involving VWF and TMEM16B/ANO2.
V Cenedese, M Mezzavilla, A Morgan, R Marino, CP Ettorre, ...
PloS one 10 (1), 2015
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Artículos 1–20