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Potential publications

12 publications found

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Group #1

Matched potential author: Lina Artifoni - author of 2 items
TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
mRNA sequencing of a novel NPHS2 intronic mutation in a child with focal and segmental glomerulosclerosis[1]Elisa Benetti, [2]Gianluca Caridi, [3]Sonia Centi, [4]Manuela Della Vella, [5]Gian Marco Ghiggeri, [6]Lina Artifoni, [7]Luisa Murer [Full author list]Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia [missing]DOI: 10.4103/1319-2442.135180 [ORCID]
PubMed: 24969201 [ORCID]
glomerulosclerosis [missing]2014-07-01Lina Artifoni (Q114778464; 2 items)
SIX1 gene: absence of mutations in children with isolated congenital anomalies of kidney and urinary tract[1]Susanna Negrisolo, [2]Sonia Centi, [3]Elisa Benetti, [4]Giulia Ghirardo, [5]Manuela Della Vella, [6]Luisa Murer, [7]Lina Artifoni [Full author list]Journal of Nephrology [missing]DOI: 10.1007/S40620-014-0112-X [ORCID]
PubMed: 24899122 [ORCID]
2014-06-05Lina Artifoni (Q114778464; 2 items)
Upper urinary tract infections are associated with RANTES promoter polymorphism[1]Sonia Centi, [2]Susanna Negrisolo, [3]Alejandra Stefanic, [4]Elisa Benetti, [5]Walburga Cassar, [6]Liviana Da Dalt, [7]Waifro Rigamonti, [8]Pietro Zucchetta, [9]Giovanni Montini, [10]Luisa Murer, [11]Lina Artifoni [Full author list]The Journal of Pediatrics [missing]DOI: 10.1016/J.JPEDS.2010.08.006 [ORCID]
PubMed: 20869067 [ORCID]
urinary tract infection [missing]2010-09-24Lina Artifoni (Q114778464; 2 items)
The impact of eNOS, MTR and MTHFR polymorphisms on renal graft survival in children and young adults[1]Lina Artifoni, [2]Elisa Benetti, [3]Sonia Centi, [4]Susanna Negrisolo, [5]Gian Marco Ghiggeri, [6]Fabrizio Ginevri, [7]Luciana Ghio, [8]Alberto Edefonti, [9]Caterina Brambilla, [10]Nicoletta Cagni, [11]Luisa Murer [Full author list]Nephrology Dialysis Transplantation [missing]DOI: 10.1093/NDT/GFP161 [ORCID]
PubMed: 19349296 [ORCID]
2009-04-06Lina Artifoni (Q114778464; 2 items)
10p12.1 deletion: HDR phenotype without DGS2 features.[1]Elisa Benetti, [2]Luisa Murer, [3]Andrea Bordugo, [4]Barbara Andreetta, [5]Lina Artifoni [Full author list]Experimental and Molecular Pathology [missing]DOI: 10.1016/J.YEXMP.2008.10.003 [ORCID]
PubMed: 19022243 [ORCID]
2008-10-31Lina Artifoni (Q114778464; 2 items)
Renal hypoplasia without optic coloboma associated with PAX2 gene deletion[1]Elisa Benetti, [2]Lina Artifoni, [3]Leonardo Salviati, [4]Luisa Pinello, [5]Silverio Perrotta, [6]Orsetta Zuffardi, [7]Graziella Zacchello, [8]Luisa Murer [Full author list]Nephrology Dialysis Transplantation [missing]DOI: 10.1093/NDT/GFM187 [ORCID]
PubMed: 17403695 [ORCID]
renal hypoplasia [missing]2007-04-01Lina Artifoni (Q114778464; 2 items)
Interleukin-8 and CXCR1 receptor functional polymorphisms and susceptibility to acute pyelonephritis[1]Lina Artifoni, [2]Susanna Negrisolo, [3]Giovanni Montini, [4]Pietro Zucchetta, [5]Pier Paolo Molinari, [6]Walburga Cassar, [7]Roberta Destro, [8]Franca Anglani, [9]Waifro Rigamonti, [10]Graziella Zacchello, [11]Luisa Murer [Full author list]Journal of Urology [missing]DOI: 10.1016/J.JURO.2006.10.037 [ORCID]
PubMed: 17296422 [ORCID]
urology [missing]; interleukins [missing]; acute pyelonephritis [missing]2007-03-01Lina Artifoni (Q114778464; 2 items)
Embryology and genetics of primary vesico-ureteric reflux and associated renal dysplasia[1]Luisa Murer, [2]Elisa Benetti, [3]Lina Artifoni [Full author list]Pediatric Nephrology [missing]DOI: 10.1007/S00467-006-0390-1 [ORCID]
PubMed: 17216254 [ORCID]
2007-01-10Lina Artifoni (Q114778464; 2 items)

Group #2

TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Identification of GDNF gene sequence variations in patients with medullary sponge kidney disease[1]Rossella Torregrossa, [2]Franca Anglani, [3]Antonia Fabris, [4]Alessia Gozzini, [5]Annalisa Tanini, [6]Dorella Del Prete, [7]Rosalba Cristofaro, [8]Lina Artifoni, [9]Cataldo Abaterusso, [10]Nicola Marchionna, [11]Antonio Lupo, [12]Angela D'Angelo, [13]Giovanni Gambaro [Full author list]Clinical Journal of the American Society of Nephrology [missing]DOI: 10.2215/CJN.07551009 [ORCID]
PubMed: 20448065 [ORCID]
medullary sponge kidney [missing]2010-05-06
Dent's disease and prevalence of renal stones in dialysis patients in Northeastern Italy[1]Enrica Tosetto, [2]Romina Graziotto, [3]Lina Artifoni, [4]Josef Nachtigal, [5]Carmelo Cascone, [6]Piero Conz, [7]Michele Piva, [8]Roberto Dell'Aquila, [9]Ermanno De Paoli Vitali, [10]Lorenzo Citron, [11]Federico Nalesso, [12]Augusto Antonello, [13]Ugo Vertolli, [14]Riccardo Zagatti, [15]Antonio Lupo, [16]Angela D'Angelo, [17]Franca Anglani, [18]Giovanni Gambaro [Full author list]Journal of Human Genetics [missing]DOI: 10.1007/S10038-005-0317-X [ORCID]
PubMed: 16247550 [ORCID]
Italy [missing]; renal dialysis [missing]2005-10-25

Misc

TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Interstitial 22q13 deletions: genes other than SHANK3 have major effects on cognitive and language development[1]Heather L Wilson, [2]John A Crolla, [3]Dena Walker, [4]Lina Artifoni, [5]Bruno Dallapiccola, [6]Takako Takano, [7]Pradeep Vasudevan, [8]Shuwen Huang, [9]Vivienne Maloney, [10]Twila Yobb, [11]Oliver Quarrell, [12]Heather E McDermid [Full author list]European Journal of Human Genetics [missing]DOI: 10.1038/EJHG.2008.107 [ORCID]
PubMed: 18523453 [ORCID]
language development [missing]2008-11-01
Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: cooperative study of 19 Italian laboratories[1]Leda Dalprà, [2]Daniela Giardino, [3]Palma Finelli, [4]Cecilia Corti, [5]Chiara Valtorta, [6]Silvana Guerneri, [7]Patrizia Ilardi, [8]Renato Fortuna, [9]Domenico Coviello, [10]Gianfranco Nocera, ..., [31]Rosario Casalone, [32]Elisabetta Lenzini, [33]Lina Artifoni, [34]Vanna Pecile, [35]Sergio Barlati, ... [Full author list]Genetics in Medicine [missing]DOI: 10.1097/01.GIM.0000182876.57766.2D [ORCID]
PubMed: 16301863 [ORCID]
2005-11-01

Potential author items

NameDescriptionAuthored itemsIdentifiersEmployer(s)
Lina Artifoniresearcher2
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