Sara Lupoli

发表

Defining the role of common variation in the genomic and biological architecture of adult human height

Ross M. Fraser, Janina M. Jeff, Audrey Y. Chu, 2014, Nature Genetics.

Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidence

J. Beckmann, L. Milanesi, D. Lancet, 2010, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Hippocampal Atrophy as a Quantitative Trait in a Genome-Wide Association Study Identifying Novel Susceptibility Genes for Alzheimer's Disease

Andrew J. Saykin, Jessica A. Turner, Steven G. Potkin, 2009, PloS one.

Identification of new schizophrenia susceptibility loci in an ethnically homogeneous, family‐based, Arab‐Israeli sample

D. Rujescu, I. Giegling, D. Lancet, 2011, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Simon C. Potter, Joseph T. Glessner, M. Pirinen, 2011, Nature.

Klotho Gene in Human Salt-Sensitive Hypertension.

L. Citterio, L. Zagato, D. Cusi, 2020, American Society of Nephrology. Clinical Journal.

Preliminary profiling of blood transcriptome in a rat model of hemorrhagic shock

G. Schmid-Schönbein, G. Baselli, S. Lupoli, 2017, Experimental biology and medicine.

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.

Sonja W. Scholz, S. Bandinelli, D. Hernandez, 2009, Human molecular genetics.

DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population.

Doron Lancet, Fabio Macciardi, Lior Greenbaum, 2012, The international journal of neuropsychopharmacology.

Association of the Type 2 Diabetes Mellitus Susceptibility Gene, TCF7L2, with Schizophrenia in an Arab-Israeli Family Sample

Doron Lancet, Fabio Macciardi, Lior Greenbaum, 2012, PloS one.

Genomewide Association Study Using a High-Density Single Nucleotide Polymorphism Array and Case-Control Design Identifies a Novel Essential Hypertension Susceptibility Locus in the Promoter Region of Endothelial NO Synthase

C. Hoggart, J. Beckmann, Z. Kutalik, 2012, Hypertension.

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

S. E. Stewart, C. Sabatti, N. Freimer, 2015, The American journal of psychiatry.

Population Stratification Analysis in Genome-Wide Association Studies

Steven G. Potkin, Alessandro Orro, Luciano Milanesi, 2011, Mathematical Approaches to Polymer Sequence Analysis and Related Problems.

Synthase Hypertension Susceptibility Locus in the Promoter Region of Endothelial NO Polymorphism Array and Case-Control Design Identifies a Novel Essential Genomewide Association Study Using a High-Density Single Nucleotide

C. Hoggart, J. Beckmann, Z. Kutalik, 2011 .

Association of Genetic Markers with CSF Oligoclonal Bands in Multiple Sclerosis Patients

A. Goris, H. Harbo, E. Celius, 2013, PloS one.

Target Sequencing, Cell Experiments, and a Population Study Establish Endothelial Nitric Oxide Synthase (eNOS) Gene as Hypertension Susceptibility Gene

J. Beckmann, J. Staessen, L. Thijs, 2013, Hypertension.

A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility

M. Filippi, P. D. De Jager, V. Martinelli, 2022, Journal of Neurology.

Genetic burden of common variants in progressive and bout-onset multiple sclerosis

V. Martinelli, G. Comi, F. Guerini, 2014, Multiple sclerosis.

Dietary Salt Intake, Blood Pressure, and Genes

E. Salvi, S. Lupoli, C. Barlassina, 2013, Current Nutrition Reports.

Pharmacogenomics considerations in the control of hypertension.

E. Salvi, S. Lupoli, C. Barlassina, 2015, Pharmacogenomics.

Replication study to confirm the role of CYP2D6 polymorphism rs1080985 on donepezil efficacy in Alzheimer's disease patients.

M. Franceschi, F. Clerici, C. Mariani, 2012, Journal of Alzheimer's disease : JAD.

Exome sequencing identifies variants in two genes encoding the LIM-proteins NRAP and FHL1 in an Italian patient with BAG3 myofibrillar myopathy

L. Milanesi, D. Cusi, S. Lupoli, 2016, Journal of Muscle Research and Cell Motility.

Interaction between polyphenols intake and PON1 gene variants on markers of cardiovascular disease: a nutrigenetic observational study

M. Turiel, E. Salvi, D. Cusi, 2016, Journal of Translational Medicine.

The burden of multiple sclerosis variants in continental Italians and Sardinians

A. Mulas, V. Martinelli, G. Comi, 2015, Multiple sclerosis.

Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis

Fabio Macciardi, Angelo Andriulli, Nicola Caporaso, 2010, Nature Genetics.

Interaction between polyphenols intake and PON1 gene variants on markers of cardiovascular disease: a nutrigenetic observational study

M. Turiel, E. Salvi, D. Cusi, 2016, Journal of Translational Medicine.

TGFβ receptor gene variants in systemic sclerosis-related pulmonary arterial hypertension: results from a multicentre EUSTAR study of European Caucasian patients

M. Humbert, M. Müller-Nurasyid, J. Cracowski, 2012, Annals of the rheumatic diseases.

Pharmacogenomics in Alzheimer's disease: a genome-wide association study of response to cholinesterase inhibitors

M. Mayhaus, M. Franceschi, F. Clerici, 2013, Neurobiology of Aging.