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Scopus Author ID: 7202171248
ResearcherID: O-1664-2016

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Employment (4)

University of Pavia: Pavia, IT

2002 to present | Associate Professor (Molecular Medicine)
Employment
Source: Self-asserted source
ELENA ROSSI

University of Pavia: Pavia, IT

2001 to 2002 | Biological researcher (Biology and Medical genetic Institute, Faculty of Medicine)
Employment
Source: Self-asserted source
ELENA ROSSI

University of Pavia: Pavia, IT

1999 to 2001 | Biological technician (Biology and Medical genetic Institute, Faculty of Medicine)
Employment
Source: Self-asserted source
ELENA ROSSI

Ospedale San Raffaele: Milano, Lombardia, IT

1997 to 1999 | Biologist (Cytogenetics laboratory)
Employment
Source: Self-asserted source
ELENA ROSSI

Education and qualifications (2)

University of Pavia: Pavia, IT

1992 to 1997 | PhD in “Human Patology” (Biology and Medical Genetic Institute, University of Pavia)
Education
Source: Self-asserted source
ELENA ROSSI

University of Pavia: Pavia, IT

1991 | postgraduate specialization degree in Human Cytogenetics
Education
Source: Self-asserted source
ELENA ROSSI

Funding (2)

High resolution array-CGH in subjects with isolated and syndromic congenital heart defects: a powerful tool to clone new critical genes and to identify the causes of genomic rearrangements

2007-02 to 2009-03 | Grant
Ministero dell’Istruzione, dell’Università e della Ricerca (Pavia, IT)
GRANT_NUMBER:

2006050014_002
Source: Self-asserted source
ELENA ROSSI

Genomic factors predisposing to the instability of chromosome 8 short arm: analysis of recurrent and sporadic rerrangements

2004-11 to 2006-12 | Grant
Ministero dell’Istruzione, dell’Università e della Ricerca (Pavia, IT)
GRANT_NUMBER:

2004059105_004

Source: Self-asserted source
ELENA ROSSI

Works (50 of 70)

Items per page:
Page 1 of 2

Identification of miRNAs Potentially Involved in Bronchiolitis Obliterans Syndrome: A Computational Study.

2016 | Journal article
DOI: 10.1371/journal.pone.0161771
PMID: 27564214
PMC: PMC5001701
Contributors: Di Carlo S; Rossi E; Politano G; Inghilleri S; Morbini P; Calabrese F; Benso A; Savino A; Cova E; Zampieri D et al.
Source: Self-asserted source
ELENA ROSSI via Europe PubMed Central

A Revised Genome Assembly of the Region 5′ to Canine SOX9 Includes the RevSex Orthologous Region

Sexual Development
2015 | Journal article
DOI: 10.1159/000435871
EID:

2-s2.0-84939567198
Contributors: Rossi, E.; Radi, O.; De Lorenzi, L.; Iannuzzi, A.; Camerino, G.; Zuffardi, O.; Parma, P.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

New cryptic karyotypic differences between cattle (Bos taurus) and goat (Capra hircus)

Chromosome Research
2015 | Journal article
DOI: 10.1007/s10577-014-9462-4
EID:

2-s2.0-84939996251
Contributors: De Lorenzi, L.; Planas, J.; Rossi, E.; Malagutti, L.; Parma, P.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

A newborn with ambiguous genitalia and a complex X;Y rearrangement

Iranian Journal of Reproductive Medicine
2014 | Journal article
EID:

2-s2.0-84939177569
Contributors: Dehghani, M.; Rossi, E.; Vetro, A.; Russo, G.; Hashemian, Z.; Zuffardi, O.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

De novo reciprocal translocation t(5;6)(q13;q34) in cattle: Cytogenetic and molecular characterization

Cytogenetic and Genome Research
2014 | Journal article
DOI: 10.1159/000356209
EID:

2-s2.0-84896839104
Contributors: De Lorenzi, L.; Rossi, E.; Gimelli, S.; Parma, P.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Defining the phenotype associated with microduplication reciprocal to Sotos syndrome microdeletion

American Journal of Medical Genetics, Part A
2014 | Journal article
DOI: 10.1002/ajmg.a.36591
EID:

2-s2.0-84904389855
Contributors: Novara, F.; Stanzial, F.; Rossi, E.; Benedicenti, F.; Inzana, F.; Di Gregorio, E.; Brusco, A.; Graakjaer, J.; Fagerberg, C.; Belligni, E. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Sox9 duplications are a relevant cause of SRY-negative XX sex reversal dogs

PLoS ONE
2014 | Journal article
DOI: 10.1371/journal.pone.0101244
EID:

2-s2.0-84904251073
Contributors: Rossi, E.; Radi, O.; De Lorenzi, L.; Vetro, A.; Groppetti, D.; Bigliardi, E.; Luvoni, G.C.; Rota, A.; Camerino, G.; Zuffardi, O. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

19q13.11 cryptic deletion: Description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadias

European Journal of Human Genetics
2012 | Journal article
DOI: 10.1038/ejhg.2012.19
EID:

2-s2.0-84864138306
Contributors: Gana, S.; Veggiotti, P.; Sciacca, G.; Fedeli, C.; Bersano, A.; Micieli, G.; Maghnie, M.; Ciccone, R.; Rossi, E.; Plunkett, K. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

De novo unbalanced translocations in Prader-Willi and Angelman syndrome might be the reciprocal product of inv dup(15)s

PLoS ONE
2012 | Journal article
DOI: 10.1371/journal.pone.0039180
EID:

2-s2.0-84862262236
Contributors: Rossi, E.; Giorda, R.; Bonaglia, M.C.; Di Candia, S.; Grechi, E.; Franzese, A.; Soli, F.; Rivieri, F.; Patricelli, M.G.; Saccilotto, D. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Genomic analysis of cattle rob(1;29)

Chromosome Research
2012 | Journal article
DOI: 10.1007/s10577-012-9315-y
EID:

2-s2.0-84875911309
Contributors: De Lorenzi, L.; Genualdo, V.; Gimelli, S.; Rossi, E.; Perucatti, A.; Iannuzzi, A.; Zannotti, M.; Malagutti, L.; Molteni, L.; Iannuzzi, L. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

High Resolution X Chromosome-Specific Array-CGH Detects New CNVs in Infertile Males

PLoS ONE
2012 | Journal article
DOI: 10.1371/journal.pone.0044887
EID:

2-s2.0-84867290682
Contributors: Krausz, C.; Giachini, C.; Lo Giacco, D.; Daguin, F.; Chianese, C.; Ars, E.; Ruiz-Castane, E.; Forti, G.; Rossi, E.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Molecular characterization of Xp chromosome deletion in a fertile cow

Sexual Development
2012 | Journal article
DOI: 10.1159/000342189
EID:

2-s2.0-84870814615
Contributors: De Lorenzi, L.; Rossi, E.; Genualdo, V.; Gimelli, S.; Lasagna, E.; Perucatti, A.; Iannuzzi, A.; Parma, P.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Correlation between genomic alterations assessed by array comparative genomic hybridization, prognostically informative histologic subtype, stage, and patient survival in gastric cancer

Human Pathology
2011 | Journal article
DOI: 10.1016/j.humpath.2011.02.016
EID:

2-s2.0-80955137447
Contributors: Rossi, E.; Klersy, C.; Manca, R.; Zuffardi, O.; Solcia, E.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Gene copy number variation in male breast cancer by aCGH

Cellular Oncology
2011 | Journal article
DOI: 10.1007/s13402-011-0041-9
EID:

2-s2.0-84870182486
Contributors: Tommasi, S.; Mangia, A.; Iannelli, G.; Chiarappa, P.; Rossi, E.; Ottini, L.; Mottolese, M.; Zoli, W.; Zuffardi, O.; Paradiso, A.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Identification of novel prognostic markers in relapsing localized resectable neuroblastoma

OMICS A Journal of Integrative Biology
2011 | Journal article
DOI: 10.1089/omi.2010.0085
EID:

2-s2.0-79952494299
Contributors: Parodi, F.; Passoni, L.; Massimo, L.; Luksch, R.; Gambini, C.; Rossi, E.; Zuffardi, O.; Pistoia, V.; Pezzolo, A.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Gene copy number variation in male breast cancer by aCGH

Analytical Cellular Pathology
2010 | Journal article
DOI: 10.3233/ACP-CLO-2010-0544
EID:

2-s2.0-79952544272
Contributors: Tommasi, S.; Mangia, A.; Iannelli, G.; Chiarappa, P.; Rossi, E.; Ottini, L.; Mottolese, M.; Zoli, W.; Zuffardi, O.; Paradiso, A.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome)

Neurogenetics
2009 | Journal article
DOI: 10.1007/s10048-008-0157-x
EID:

2-s2.0-64149094521
Contributors: Coldren, C.D.; Lai, Z.; Shragg, P.; Rossi, E.; Glidewell, S.C.; Zuffardi, O.; Mattina, T.; Ivy, D.D.; Curfs, L.M.; Mattson, S.N. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Presence of 1q gain and absence of 7p gain are new predictors of local or metastatic relapse in localized resectable neuroblastoma

Neuro-Oncology
2009 | Journal article
DOI: 10.1215/15228517-2008-086
EID:

2-s2.0-65949100780
Contributors: Pezzolo, A.; Rossi, E.; Gimelli, S.; Parodi, F.; Negri, F.; Conte, M.; Pistorio, A.; Sementa, A.; Pistoia, V.; Zuffardi, O. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

A 12 Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea

European Journal of Medical Genetics
2008 | Journal article
DOI: 10.1016/j.ejmg.2008.06.010
EID:

2-s2.0-56649085194
Contributors: Rossi, E.; Verri, A.P.; Patricelli, M.G.; Destefani, V.; Ricca, I.; Vetro, A.; Ciccone, R.; Giorda, R.; Toniolo, D.; Maraschio, P. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

A prenatal case of duplication with terminal deletion of 5p not identified by conventional cytogenetics

Prenatal Diagnosis
2008 | Journal article
DOI: 10.1002/pd.2132
EID:

2-s2.0-57149111959
Contributors: Vetro, A.; Iasci, A.; Dal Bello, B.; Rossi, E.; Messa, J.; Montanari, L.; Cesari, S.; Zuffardi, O.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome

Journal of Medical Genetics
2008 | Journal article
DOI: 10.1136/jmg.2008.058701
EID:

2-s2.0-56049085381
Contributors: Koolen, D.A.; Sharp, A.J.; Hurst, J.A.; Firth, H.V.; Knight, S.J.L.; Goldenberg, A.; Saugier-Veber, P.; Pfundt, R.; Vissers, L.E.L.M.; Destrée, A. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: Clues to the mechanisms of formation

Journal of Medical Genetics
2008 | Journal article
DOI: 10.1136/jmg.2007.054007
EID:

2-s2.0-40649085830
Contributors: Rossi, E.; Riegel, M.; Messa, J.; Gimelli, S.; Maraschio, P.; Ciccone, R.; Stroppi, M.; Riva, P.; Perrotta, C.S.; Mattina, T. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Familial translocation t(3;10) (p26.3;p12.31) leading to trisomy 10p12.31 → pter and monosomy 3p26.3 → pter in seven members

American Journal of Medical Genetics, Part A
2008 | Journal article
DOI: 10.1002/ajmg.a.32590
EID:

2-s2.0-57149108009
Contributors: Nucaro, A.L.; Meloni, M.; Pisano, T.; Melis, P.; Rossi, E.; Rossino, R.; Corona, S.; Loi, M.; Achena, F.; Zuffardi, O. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Ring syndrome: Still true?

Journal of Medical Genetics
2008 | Journal article
DOI: 10.1136/jmg.2008.060442
EID:

2-s2.0-55449125578
Contributors: Rossi, E.; Messa, J.; Zuffardi, O.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients.

Journal of medical genetics
2007 | Journal article
EID:

2-s2.0-33846898823
Contributors: Ballarati, L.; Rossi, E.; Bonati, M.T.; Gimelli, S.; Maraschio, P.; Finelli, P.; Giglio, S.; Lapi, E.; Bedeschi, M.F.; Guerneri, S. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: A study of 59 patients

Journal of Medical Genetics
2007 | Journal article
DOI: 10.1136/jmg.2007.052787
EID:

2-s2.0-37249022297
Contributors: De Gregori, M.; Ciccone, R.; Magini, P.; Pramparo, T.; Gimelli, S.; Messa, J.; Novara, F.; Vetro, A.; Rossi, E.; Maraschio, P. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Deletion of a 760 kb region at 4p16 determines the prenatal and postnatal growth retardation characteristic of Wolf-Hirschhorn syndrome

Journal of Medical Genetics
2007 | Journal article
DOI: 10.1136/jmg.2007.050963
EID:

2-s2.0-35348891957
Contributors: Concolino, D.; Rossi, E.; Strisciuglio, P.; Iembo, M.A.; Giorda, R.; Ciccone, R.; Tenconi, R.; Zuffardi, O.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Chromosomal rearrangements in Xq and premature ovarian failure: Mapping of 25 new cases and review of the literature

Human Reproduction
2006 | Journal article
DOI: 10.1093/humrep/dei495
EID:

2-s2.0-33646496697
Contributors: Rizzolio, F.; Bione, S.; Sala, C.; Goegan, M.; Gentile, M.; Gregato, G.; Rossi, E.; Pramparo, T.; Zuffardi, O.; Toniolo, D.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

8.5 Mb deletion at distal 5p in a male ascertained for azoospermia

American Journal of Medical Genetics
2005 | Journal article
DOI: 10.1002/ajmg.a.30519
EID:

2-s2.0-14044249492
Contributors: Rossi, E.; De Gregori, M.; Patricelli, M.G.; Pramparo, T.; Argentiero, L.; Giglio, S.; Sosta, K.; Foresti, G.; Zuffardi, O.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Reciprocal translocations: A trap for cytogenetists?

Human Genetics
2005 | Journal article
DOI: 10.1007/s00439-005-1324-x
EID:

2-s2.0-27544490144
Contributors: Ciccone, R.; Giorda, R.; Gregato, G.; Guerrini, R.; Giglio, S.; Carrozzo, R.; Bonaglia, M.C.; Priolo, E.; Laganà, C.; Tenconi, R. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Partial trisomy 7q22-q34 due to malsegregation of a complex chromosomal rearrangement involving five chromosomes in a girl with mental retardation and multiple congenital malformations

Italian Journal of Pediatrics
2004 | Journal article
EID:

2-s2.0-11144229718
Contributors: Concolino, D.; Lembo, M.A.; Rossi, E.; Moricca, M.T.; Strisciuglio, P.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Subtelomeric deletions of chromosome 9q: A novel microdeletion syndrome

American Journal of Medical Genetics
2004 | Journal article
EID:

2-s2.0-3342894655
Contributors: Stewart, D.R.; Huang, A.; Faravelli, F.; Anderlid, B.-M.; Medne, L.; Ciprero, K.; Kaur, M.; Rossi, E.; Tenconi, R.; Nordenskjöld, M. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Cryptic t(1;12)(q44;p13.3) translocation in a previously described syndrome with polymicrogyria, segregating as an apparently X-linked trait

American Journal of Medical Genetics
2003 | Journal article
EID:

2-s2.0-0038412585
Contributors: Zollino, M.; Colosimo, C.; Zuffardi, O.; Rossi, E.; Tosolini, A.; Walsh, C.A.; Neri, G.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Ring Chromosome 10 (p15q26) in a Patient with Unipolar Affective Disorder, Multiple Minor Anomalies, and Mental Retardation [4]

American Journal of Medical Genetics
2003 | Journal article
EID:

2-s2.0-0242426664
Contributors: Concolino, D.; Iembo, M.A.; Moricca, M.T.; Strisciuglio, P.; Marotta, R.; Rossi, E.; Giglio, S.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Alport syndrome and mental retardation: Clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR) [7]

Journal of Medical Genetics
2002 | Journal article
EID:

2-s2.0-18344377865
Contributors: Meloni, I.; Vitelli, F.; Pucci, L.; Lowry, R.B.; Tonlorenzi, R.; Rossi, E.; Ventura, M.; Rizzoni, G.; Kashtan, C.E.; Pober, B. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Familial pericentric inversion of chromosome 5 in a family with benign neonatal convulsions [9]

Journal of Medical Genetics
2002 | Journal article
EID:

2-s2.0-0036196133
Contributors: Concolino, D.; Iembo, M.A.; Rossi, E.; Giglio, S.; Coppola, G.; Del Giudice, E.M.; Strisciuglio, P.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Case of Myhre syndrome with autism and peculiar skin histological findings

American Journal of Medical Genetics
2001 | Journal article
DOI: 10.1002/ajmg.1517
EID:

2-s2.0-0035479340
Contributors: Titomanlio, L.; Marzano, M.G.; Rossi, E.; D'Armiento, M.; De Brasi, D.; Vega, G.R.; Andreucci, M.V.; Orsini, A.V.M.; Santoro, L.; Sebastio, G.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations [9]

Journal of Medical Genetics
2001 | Journal article
EID:

2-s2.0-0034979654
Contributors: Rossi, E.; Piccini, F.; Zollino, M.; Neri, G.; Caselli, D.; Tenconi, R.; Castellan, C.; Carrozzo, R.; Danesino, C.; Zuffardi, O. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Inv dup del (1)(pter→q44::q44→q42:) with the classical phenotype of trisomy 1q42-qter

American Journal of Medical Genetics
2001 | Journal article
DOI: 10.1002/ajmg.1589
EID:

2-s2.0-0035935632
Contributors: De Brasi, D.; Rossi, E.; Giglio, S.; D'Agostino, A.; Titomanlio, L.; Farina, V.; Andria, G.; Sebastio, G.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Cytogenetic abnormalities in PHA-stimulated lymphocytes from patients with langerhans cell histiocytosis

British Journal of Haematology
2000 | Journal article
DOI: 10.1046/j.1365-2141.2000.02313.x
EID:

2-s2.0-0033764984
Contributors: Scappaticci, S.; Danesino, C.; Rossi, E.; Klersy, C.; Fiori, G.M.; Clementi, R.; Russotto, V.S.; Bossi, G.; Aricò, M.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects

Circulation
2000 | Journal article
EID:

2-s2.0-0034713818
Contributors: Giglio, S.; Graw, S.L.; Gimelli, G.; Pirola, B.; Varone, P.; Voullaire, L.; Lerzo, F.; Rossi, E.; Dellavecchia, C.; Bonaglia, M.C. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency

Clinical Genetics
2000 | Journal article
DOI: 10.1034/j.1399-0004.2000.570510.x
EID:

2-s2.0-0034011273
Contributors: Nowaczyk, M.J.M.; Huggins, M.J.; Tomkins, D.J.; Rossi, E.; Ramsay, J.A.; Woulfe, J.; Scherer, S.W.; Belloni, E.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Inverted duplications are recurrent rearrangements always associated with a distal deletion: Description of a new case involving 2q

European Journal of Human Genetics
2000 | Journal article
DOI: 10.1038/sj.ejhg.5200509
EID:

2-s2.0-0033872079
Contributors: Bonaglia, M.C.; Giorda, R.; Poggi, G.; Raggi, M.E.; Rossi, E.; Baroncini, A.; Giglio, S.; Borgatti, R.; Zuffardi, O.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Cloning and characterization of NEU2, a human gene homologous to rodent soluble sialidases

Genomics
1999 | Journal article
DOI: 10.1006/geno.1999.5749
EID:

2-s2.0-0033118290
Contributors: Monti, E.; Preti, A.; Rossi, E.; Ballabio, A.; Borsani, G.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Identification and characterization of CDS2, a mammalian homolog of the Drosophila CDP-diacylglycerol synthase gene

Genomics
1999 | Journal article
DOI: 10.1006/geno.1998.5610
EID:

2-s2.0-0032956113
Contributors: Volta, M.; Bulfone, A.; Gattuso, C.; Rossi, E.; Mariani, M.; Consalez, G.G.; Zuffardi, O.; Ballabio, A.; Banfi, S.; Franco, B.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Intracellular levels of the LIS1 protein correlate with clinical and neuroradiological findings in patients with classical lissencephaly

Annals of Neurology
1999 | Journal article
DOI: 10.1002/1531-8249(199902)45:2<154::AID-ANA4>3.0.CO;2-P
EID:

2-s2.0-0033042045
Contributors: Fogli, A.; Guerrini, R.; Moro, F.; Fernandez-Alvarez, E.; Livet, M.O.; Renieri, A.; Cioni, M.; Pilz, D.T.; Veggiotti, P.; Rossi, E. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Chromosome 20 ring: A chromosomal disorder associated with a particular electroclinical pattern

Epilepsia
1998 | Journal article
DOI: 10.1111/j.1528-1157.1998.tb01443.x
EID:

2-s2.0-0031684193
Contributors: Canevini, M.P.; Sgro, V.; Zuffardi, O.; Canger, R.; Carrozzo, R.; Rossi, E.; Ledbetter, D.; Minicucci, F.; Vignoli, A.; Piazzini, A. et al.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Human FIGF: Cloning, gene structure, and mapping to chromosome Xp22.1 between the PIGA and the GRPR genes

Genomics
1998 | Journal article
DOI: 10.1006/geno.1997.5079
EID:

2-s2.0-0032518387
Contributors: Rocchigiani, M.; Lestingi, M.; Luddi, A.; Orlandini, M.; Franco, B.; Rossi, E.; Ballabio, A.; Zuffardi, O.; Oliviero, S.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

Identification and characterization of a novel member of the dystrobrevin gene family

FEBS Letters
1998 | Journal article
DOI: 10.1016/S0014-5793(98)00097-0
EID:

2-s2.0-0032549565
Contributors: Puca, A.A.; Nigro, V.; Piluso, G.; Belsito, A.; Sampaolo, S.; Quaderi, N.; Rossi, E.; Di Iorio, G.; Ballabio, A.; Franco, B.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier

The gene encoding a cationic amino acid transporter (SLC7A4) maps to the region deleted in the velocardiofacial syndrome

Genomics
1998 | Journal article
DOI: 10.1006/geno.1998.5252
EID:

2-s2.0-0032522236
Contributors: Sperandeo, M.P.; Borsani, G.; Incerti, B.; Zollo, M.; Rossi, E.; Zuffardi, O.; Castaldo, P.; Taglialatela, M.; Andria, G.; Sebastio, G.
Source: Self-asserted source
ELENA ROSSI via Scopus - Elsevier
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Peer review (3 reviews for 2 publications/grants)

Review activity for Human genetics. (2)
Review activity for International journal of molecular sciences. (1)
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