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Alberto Magi

Showing results (31-40 of 83) with videos related to

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Communications Biology|November 3, 2021
Charting differentially methylated regions in cancer with Rocker-methMatteo Benelli, Gian Marco Franceschini, Alberto Magi, et al.
Biostatistics (Oxford, England)|March 9, 2010
A very fast and accurate method for calling aberrations in array-CGH dataMatteo Benelli, Giuseppina Marseglia, Genni Nannetti, et al.
Biomed Research International|September 27, 2018
Bicuspid Aortic Valve: Role of Multiple Gene Variants in Influencing the Clinical PhenotypeElena Sticchi, Rosina De Cario, Alberto Magi, et al.
Bioinformatics (Oxford, England)|November 4, 2005
Using a calibration experiment to assess gene-specific information: full Bayesian and empirical Bayesian models for two-channel microarray dataMarta Blangiardo, Simona Toti, Betti Giusti, et al.
Journal of Orthopaedic Surgery and Research|November 8, 2018
Rationale and pre-clinical evidences for the use of autologous cartilage micrografts in cartilage repairMarco Viganò, Irene Tessaro, Letizia Trovato, et al.
Human Heredity|August 19, 2011
EX-HOM (EXome HOMozygosity): a proof of principleTommaso Pippucci, Matteo Benelli, Alberto Magi, et al.
Molecular Cancer|February 13, 2021
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patientsFilippo Martignano, Uday Munagala, Stefania Crucitta, et al.
Plos One|February 23, 2016
Apolipoprotein(a) Kringle-IV Type 2 Copy Number Variation Is Associated with Venous ThromboembolismElena Sticchi, Alberto Magi, Pia R Kamstrup, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|January 2, 2009
Assessment of fibrinolytic activity by measuring the lysis time of a tissue-factor-induced clot: a feasibility evaluationAnna Paola Cellai, Donatella Lami, Alberto Magi, et al.
European Journal of Medical Genetics|February 16, 2012
372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairmentGiuseppina Marseglia, Maria Rosaria Scordo, Chiara Pescucci, et al.
Pageof 9

Showing results (31-40 of 83) with videos related to

Sort By:
Pageof 9
Communications Biology|November 3, 2021
Charting differentially methylated regions in cancer with Rocker-methMatteo Benelli, Gian Marco Franceschini, Alberto Magi, et al.
Biostatistics (Oxford, England)|March 9, 2010
A very fast and accurate method for calling aberrations in array-CGH dataMatteo Benelli, Giuseppina Marseglia, Genni Nannetti, et al.
Biomed Research International|September 27, 2018
Bicuspid Aortic Valve: Role of Multiple Gene Variants in Influencing the Clinical PhenotypeElena Sticchi, Rosina De Cario, Alberto Magi, et al.
Bioinformatics (Oxford, England)|November 4, 2005
Using a calibration experiment to assess gene-specific information: full Bayesian and empirical Bayesian models for two-channel microarray dataMarta Blangiardo, Simona Toti, Betti Giusti, et al.
Journal of Orthopaedic Surgery and Research|November 8, 2018
Rationale and pre-clinical evidences for the use of autologous cartilage micrografts in cartilage repairMarco Viganò, Irene Tessaro, Letizia Trovato, et al.
Human Heredity|August 19, 2011
EX-HOM (EXome HOMozygosity): a proof of principleTommaso Pippucci, Matteo Benelli, Alberto Magi, et al.
Molecular Cancer|February 13, 2021
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patientsFilippo Martignano, Uday Munagala, Stefania Crucitta, et al.
Plos One|February 23, 2016
Apolipoprotein(a) Kringle-IV Type 2 Copy Number Variation Is Associated with Venous ThromboembolismElena Sticchi, Alberto Magi, Pia R Kamstrup, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|January 2, 2009
Assessment of fibrinolytic activity by measuring the lysis time of a tissue-factor-induced clot: a feasibility evaluationAnna Paola Cellai, Donatella Lami, Alberto Magi, et al.
European Journal of Medical Genetics|February 16, 2012
372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairmentGiuseppina Marseglia, Maria Rosaria Scordo, Chiara Pescucci, et al.
Pageof 9