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Mostrati risultati da 1 a 20 di 81
Titolo Data di pubblicazione Autore(i) File
Hypnotizability and polymorphisms of the COMT gene: an association study 1-gen-2011 Presciuttini, S; Gialluisi, A; Barbuti, S; Curcio, M; Scatena, F; Ghelarducci, B; Santarcangelo, El; Carli, G.
Estimating the prevalence of autosomal recessive disorders through mutational records and consanguinity: the Homozygosity Index (HI) 1-gen-2011 Gialluisi, A; Pippucci, T; Anikster, Y; Ozbek, U; Medlej-Hashim, M; Mégarbané, A; Romeo, G
Estimating the prevalence of 21-hydroxylase deficiency in Italy through a novel molecular epidemiology approach 1-gen-2011 Graziano, C; Gialluisi, A; Baldazzi, L; Balsamo, A; Menabò, S; Romeo, G
The past, present and future of consanguinity studies 1-gen-2011 Romeo, G; Gialluisi, A; Pippucci, T
Consanguinity studies and genome research in Mediterranean developing countries 1-gen-2012 Romeo, G; Gialluisi, A; Pippucci, T
The Homozygosity Index (HI) approach reveals high allele frequency for Wilson Disease in the Sardinian population 1-gen-2012 Gialluisi, A; Incollu, S; Pippucci, T; Lepori, Mb; Zappu, A; Loudianos, G; Romeo, G
Estimating the allele frequency of autosomal recessive disorders through mutational records and consanguinity: The homozygosity index 1-gen-2012 Gialluisi, A; Pippucci, T; Anikster, Y; Ozbek, U; Medlej-Hashim, M; Mégarbané, A; Romeo, G
The homozygosity index (HI) approach reveals high allele frequency for Wilson disease in the Sardinian population 1-gen-2013 Gialluisi, A; Incollu, S; Pippucci, T; Lepori, Mb; Zappu, A; Loudianos, G; Romeo, G
Persistence and transmission of recessive deafness and sign language: New insights from village sign languages 1-gen-2013 Gialluisi, A; Dediu, D; Francks, C; Fisher, Se
Reply to ten Kate et al 1-gen-2013 Gialluisi, A; Pippucci, T; Romeo, G
Genome-wide screening for DNA variants associated with dyslexia and language impairment 1-gen-2014 Gialluisi, A; Newbury, Df; Wilcutt, Eg; Olson, Rk; Brandler, Wm; Paracchini, S; Monaco, P; Francks, C; Fisher, Se
H3M2: detection of runs of homozygosity from whole-exome sequencing data 1-gen-2014 Magi, A; Tattini, L; Palombo, F; Benelli, M; Gialluisi, A; Giusti, B; Abbate, R; Seri, M; Gensini, Gf; Romeo, G; Pippucci, T
Genome-wide screening for DNA variants associated with reading and language traits 1-gen-2014 Gialluisi, A; Newbury, Df; Wilcutt, Eg; Olson, Rk; Defries, Jc; Brandler, Wm; Pennington, Bf; Smith, Sd; Scerri, Ts; Simpson, Nh; Sli, Consortium; Luciano, M; Evans DM, ; Bates, Tc; Stein, Jf; Talcott, Jb; Monaco, Ap; Paracchini, S; Francks, C; Fisher SE,
Detection of runs of homozygosity from whole exome sequencing data: state of the art and perspectives for clinical, population and epidemiological studies 1-gen-2014 Pippucci, T; Magi, A; Gialluisi, A; Romeo, G
Hypnotizability and Catechol-O-Methyltransferase (COMT) polymorphysms in Italians 1-gen-2014 Presciuttini, S; Gialluisi, A; Barbuti, S; Curcio, M; Scatena, F; Carli, G; Santarcangelo, El
Investigating the effects of copy number variants on reading and language performance 1-gen-2016 Gialluisi, A; Visconti, A; Willcutt, Eg; Smith, Sd; Pennington, Bf; Falchi, M; Defries, Jc; Olson, Rk; Francks, C; Fisher, Se
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity 1-gen-2017 Joshi, Pk; Pirastu, N; Kentistou, Ka; Fischer, K; Hofer, E; Schraut, Ke; Clark, Dw; Nutile, T; Barnes, Clk; Timmers, Prhj; Shen, X; Gandin, I; Mcdaid, Af; Hansen, Tf; Gordon, Sd; Giulianini, F; Boutin, Ts; Abdellaoui, A; Zhao, W; Medina-Gomez, C; Bartz, Tm; Trompet, S; Lange, La; Raffield, L; van der Spek, A; Galesloot, Te; Proitsi, P; Yanek, Lr; Bielak, Lf; Payton, A; Murgia, F; Concas, Mp; Biino, G; Tajuddin, Sm; Seppälä, I; Amin, N; Boerwinkle, E; Børglum, Ad; Campbell, A; Demerath, Ew; Demuth, I; Faul, Jd; Ford, I; Gialluisi, A; Gögele, M; Graff, M; Hingorani, A; Hottenga, Jj; Hougaard, Dm; Hurme, Ma; Ikram, Ma; Jylhä, M; Kuh, D; Ligthart, L; Lill, Cm; Lindenberger, U; Lumley, T; Mägi, R; Marques-Vidal, P; Medland, Se; Milani, L; Nagy, R; Ollier, Wer; Peyser, Pa; Pramstaller, Pp; Ridker, Pm; Rivadeneira, F; Ruggiero, D; Saba, Y; Schmidt, R; Schmidt, H; Slagboom, Pe; Smith, Bh; Smith, Ja; Sotoodehnia, N; Steinhagen-Thiessen, E; van Rooij, Fja; Verbeek, Al; Vermeulen, Sh; Vollenweider, P; Wang, Y; Werge, T; Whitfield, Jb; Zonderman, Ab; Lehtimäki, T; Evans, Mk; Pirastu, M; Fuchsberger, C; Bertram, L; Pendleton, N; Kardia, Slr; Ciullo, M; Becker, Dm; Wong, A; Psaty, Bm; van Duijn, Cm; Wilson, Jg; Jukema, Jw; Kiemeney, L; Uitterlinden, Ag; Franceschini, N; North, Ke; Weir, Dr; Metspalu, A; Boomsma, Di; Hayward, C; Chasman, D; Martin, Ng; Sattar, N; Campbell, H; Esko, T; Kutalik, Z; Wilson, Jf.
Neuroimaging genetic analyses of novel candidate genes associated with reading and language 1-gen-2017 Gialluisi, A; Guadalupe, T; Francks, C; Fisher, Se
Investigating the relation between mental health and low grade inflammation 1-gen-2018 Gialluisi, A; Bonaccio, M; Di Castelnuovo, A; Costanzo, S; De Curtis, A; Sarchiapone, M; Cerletti, C; Donati, Mb; de Gaetano, G; Iacoviello, L
INVESTIGATING THE RELATION BETWEEN MENTAL HEALTH AND LOW GRADE INFLAMMATION 1-gen-2018 Gialluisi, A; Bonaccio, M; Di Castelnuovo, A; Costanzo, S; De Curtis, A; Sarchiapone, M; Cerletti, C; Donati, Mb; de Gaetano, G; Iacoviello, L
Mostrati risultati da 1 a 20 di 81
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