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Gasparini, Paolo
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Preferred name
Gasparini, Paolo
Main Affiliation
Email
paolo.gasparini@burlo.trieste.it
ORCID
Scopus Author ID
22634397400
Researcher ID
B-6173-2014
Research Output
Now showing 1 - 10 of 21
- PublicationHearing function: Identification of new candidate genes further explaining the complexity of this sensory ability
; ; ; ;Nagtegaal A.P. ;Oosterloo B.C. ;Seshadri S. ;Heard-Costa N. ;Van Camp G. ;Fransen E. ;Francescatto M. ;Logroscino G. ;Sardone R. ;Quaranta N.; - PublicationNatural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates
;Spedicati Beatrice; ;Palmisano Roberto; ;Barbieri Caterina ;Francescatto Margherita; ; ;Pelliccione Giulia; ; - PublicationGenome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
;Simcoe Mark ;Valdes Ana ;Liu Fan ;Furlotte Nicholas A. ;Evans David M. ;Hemani Gibran ;Ring Susan M. ;Smith George Davey ;Duffy David L. ;Zhu Gu ;Gordon Scott D. ;Medland Sarah E. ;Vuckovic Dragana; ;Sala Cinzia; ; ;Brumat Marco; ;Toniolo Daniela; ; ;Yazar Seyhan ;Hewitt Alex ;Wu Wenting ;Kraft Peter ;Hammond Christopher J. ;Shi Yuan ;Chen Yan ;Zeng Changqing ;Klaver Caroline C.W. ;Uitterlinden Andre G. ;Ikram M. Arfan ;Hamer Merel A. ;van Duijn Cornelia M. ;Nijsten Tamar ;Han Jiali ;Mackey David A. ;Martin Nicholas G. ;Cheng Ching Yu ;the 23andMe Research Team ;the International Visible Trait Genetics Consortium Gruppo ;Hinds David A. ;Spector Timothy D. ;Kayser ManfredHysi Pirro G. - PublicationRuns of homozygosity are associated with staging of periodontitis in isolated populations
; ; ;Di Lenarda Roberto; ;Bevilacqua Lorenzo; - PublicationSystematic analysis of factors that improve homologous direct repair (HDR) efficiency in CRISPR/Cas9 technique
; ;Foschi Nicola ;Athanasakis Emmanouil; ; - PublicationTaste perception and expression in stomach of bitter taste receptor tas2r38 in obese and lean subjects
; ;Rosso Natalia ;Guerra Martina ;Corleone Pio ;Casagranda Biagio ;Giraudi Pablo J. ;Tiribelli Claudio ;Simeth Catrin ;Monica Fabio; ; ;de Manzini Nicolò ;Palmisano Silvia - PublicationVariants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss
;Bassani Sissy ;Van Beelen Edward ;Rossel Mireille ;Voisin Norine; ;Arribat Yoan ;Chatron Nicolas ;Chrast Jacqueline; ;Delprat Benjamin; ;Giannuzzi Giuliana ;Guex Nicolas ;Machavoine Roxane ;Pradervand Sylvain ;Smits Jeroen J. ;Van De Kamp Jiddeke M. ;Ziegler Alban ;Amati Francesca ;Marlin Sandrine ;Kremer Hannie ;Locher Heiko ;Maurice Tangui; ; Reymond Alexandre - PublicationSPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females
;Gasparini Paolo Gruppo ;Radio Francesca Clementina ;Pang Kaifang ;Ciolfi Andrea ;Levy Michael A. ;Hernández-García Andrés ;Pedace Lucia ;Pantaleoni Francesca ;Liu Zhandong ;de Boer Elke ;Jackson Adam ;Bruselles Alessandro ;McConkey Haley ;Stellacci Emilia ;Lo Cicero Stefania ;Motta Marialetizia ;Carrozzo Rosalba ;Dentici Maria Lisa ;McWalter Kirsty ;Desai Megha ;Monaghan Kristin G. ;Telegrafi Aida ;Philippe Christophe ;Vitobello Antonio ;Au Margaret ;Grand Katheryn ;Sanchez-Lara Pedro A. ;Baez Joanne ;Lindstrom Kristin ;Kulch Peggy ;Sebastian Jessica ;Madan-Khetarpal Suneeta ;Roadhouse Chelsea ;MacKenzie Jennifer J. ;Monteleone Berrin ;Saunders Carol J. ;Jean Cuevas July K. ;Cross Laura ;Zhou Dihong ;Hartley Taila ;Sawyer Sarah L. ;Monteiro Fabíola Paoli ;Secches Tania Vertemati ;Kok Fernando ;Schultz-Rogers Laura E.; ; ; ; ;Dallapiccola BrunoTartaglia Marco - PublicationGenetic dissection of temperament personality traits in Italian isolates
; ;Minelli Alessandra ;Aere Susanna; ;Tesolin Paola; ;Gennarelli Massimo
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