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Forabosco

Showing results (231-240 of 243) with videos related to

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Brain : a Journal of Neurology|September 5, 2020
Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disordersNiccolò E Mencacci, Regina Reynolds, Sonia Garcia Ruiz, et al.
Human Genetics|March 10, 1999
Exclusion of the Sonic Hedgehog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopmentM Seri, G Martucciello, L Paleari, et al.
Plos Genetics|February 2, 2011
Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasisSilvia Tore, Stefania Casula, Giuseppina Casu, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus--a GISC studyV Annese, A Latiano, P Bovio, et al.
Plos Genetics|September 27, 2013
Predicting the risk of rheumatoid arthritis and its age of onset through modelling genetic risk variants with smokingIan C Scott, Seth D Seegobin, Sophia Steer, et al.
American Journal of Human Genetics|December 23, 2006
Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy lociLuigi Bisceglia, Giuseppina Cerullo, Paola Forabosco, et al.
Genes and Immunity|September 15, 2006
Meta-analysis of genome-wide linkage studies of systemic lupus erythematosusP Forabosco, J D Gorman, C Cleveland, et al.
British Journal of Haematology|November 20, 2020
A Sardinian founder mutation in glycoprotein Ib platelet subunit beta (GP1BB) that impacts thrombocytopeniaFabio Busonero, Maristella Steri, Valeria Orrù, et al.
European Journal of Human Genetics : EJHG|January 14, 2010
Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopyEmmanuelle Bouzigon, Paola Forabosco, Gerard H Koppelman, et al.
American Journal of Human Genetics|May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaNiccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, et al.
Pageof 25

Showing results (231-240 of 243) with videos related to

Sort By:
Pageof 25
Brain : a Journal of Neurology|September 5, 2020
Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disordersNiccolò E Mencacci, Regina Reynolds, Sonia Garcia Ruiz, et al.
Human Genetics|March 10, 1999
Exclusion of the Sonic Hedgehog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopmentM Seri, G Martucciello, L Paleari, et al.
Plos Genetics|February 2, 2011
Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasisSilvia Tore, Stefania Casula, Giuseppina Casu, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus--a GISC studyV Annese, A Latiano, P Bovio, et al.
Plos Genetics|September 27, 2013
Predicting the risk of rheumatoid arthritis and its age of onset through modelling genetic risk variants with smokingIan C Scott, Seth D Seegobin, Sophia Steer, et al.
American Journal of Human Genetics|December 23, 2006
Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy lociLuigi Bisceglia, Giuseppina Cerullo, Paola Forabosco, et al.
Genes and Immunity|September 15, 2006
Meta-analysis of genome-wide linkage studies of systemic lupus erythematosusP Forabosco, J D Gorman, C Cleveland, et al.
British Journal of Haematology|November 20, 2020
A Sardinian founder mutation in glycoprotein Ib platelet subunit beta (GP1BB) that impacts thrombocytopeniaFabio Busonero, Maristella Steri, Valeria Orrù, et al.
European Journal of Human Genetics : EJHG|January 14, 2010
Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopyEmmanuelle Bouzigon, Paola Forabosco, Gerard H Koppelman, et al.
American Journal of Human Genetics|May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaNiccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, et al.
Pageof 25