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Items: 1 to 50 of 79

1.

Origins of DNA methylation defects in Wilms tumors.

Anvar Z, Acurzio B, Roma J, Cerrato F, Verde G.

Cancer Lett. 2019 Aug 10;457:119-128. doi: 10.1016/j.canlet.2019.05.013. Epub 2019 May 16.

PMID:
31103718
2.

Genome-wide association study identifies 30 loci associated with bipolar disorder.

Stahl EA, Breen G, Forstner AJ, McQuillin A, Ripke S, Trubetskoy V, Mattheisen M, Wang Y, Coleman JRI, Gaspar HA, de Leeuw CA, Steinberg S, Pavlides JMW, Trzaskowski M, Byrne EM, Pers TH, Holmans PA, Richards AL, Abbott L, Agerbo E, Akil H, Albani D, Alliey-Rodriguez N, Als TD, Anjorin A, Antilla V, Awasthi S, Badner JA, Bækvad-Hansen M, Barchas JD, Bass N, Bauer M, Belliveau R, Bergen SE, Pedersen CB, Bøen E, Boks MP, Boocock J, Budde M, Bunney W, Burmeister M, Bybjerg-Grauholm J, Byerley W, Casas M, Cerrato F, Cervantes P, Chambert K, Charney AW, Chen D, Churchhouse C, Clarke TK, Coryell W, Craig DW, Cruceanu C, Curtis D, Czerski PM, Dale AM, de Jong S, Degenhardt F, Del-Favero J, DePaulo JR, Djurovic S, Dobbyn AL, Dumont A, Elvsåshagen T, Escott-Price V, Fan CC, Fischer SB, Flickinger M, Foroud TM, Forty L, Frank J, Fraser C, Freimer NB, Frisén L, Gade K, Gage D, Garnham J, Giambartolomei C, Pedersen MG, Goldstein J, Gordon SD, Gordon-Smith K, Green EK, Green MJ, Greenwood TA, Grove J, Guan W, Guzman-Parra J, Hamshere ML, Hautzinger M, Heilbronner U, Herms S, Hipolito M, Hoffmann P, Holland D, Huckins L, Jamain S, Johnson JS, Juréus A, Kandaswamy R, Karlsson R, Kennedy JL, Kittel-Schneider S, Knowles JA, Kogevinas M, Koller AC, Kupka R, Lavebratt C, Lawrence J, Lawson WB, Leber M, Lee PH, Levy SE, Li JZ, Liu C, Lucae S, Maaser A, MacIntyre DJ, Mahon PB, Maier W, Martinsson L, McCarroll S, McGuffin P, McInnis MG, McKay JD, Medeiros H, Medland SE, Meng F, Milani L, Montgomery GW, Morris DW, Mühleisen TW, Mullins N, Nguyen H, Nievergelt CM, Adolfsson AN, Nwulia EA, O'Donovan C, Loohuis LMO, Ori APS, Oruc L, Ösby U, Perlis RH, Perry A, Pfennig A, Potash JB, Purcell SM, Regeer EJ, Reif A, Reinbold CS, Rice JP, Rivas F, Rivera M, Roussos P, Ruderfer DM, Ryu E, Sánchez-Mora C, Schatzberg AF, Scheftner WA, Schork NJ, Shannon Weickert C, Shehktman T, Shilling PD, Sigurdsson E, Slaney C, Smeland OB, Sobell JL, Søholm Hansen C, Spijker AT, St Clair D, Steffens M, Strauss JS, Streit F, Strohmaier J, Szelinger S, Thompson RC, Thorgeirsson TE, Treutlein J, Vedder H, Wang W, Watson SJ, Weickert TW, Witt SH, Xi S, Xu W, Young AH, Zandi P, Zhang P, Zöllner S; eQTLGen Consortium; BIOS Consortium, Adolfsson R, Agartz I, Alda M, Backlund L, Baune BT, Bellivier F, Berrettini WH, Biernacka JM, Blackwood DHR, Boehnke M, Børglum AD, Corvin A, Craddock N, Daly MJ, Dannlowski U, Esko T, Etain B, Frye M, Fullerton JM, Gershon ES, Gill M, Goes F, Grigoroiu-Serbanescu M, Hauser J, Hougaard DM, Hultman CM, Jones I, Jones LA, Kahn RS, Kirov G, Landén M, Leboyer M, Lewis CM, Li QS, Lissowska J, Martin NG, Mayoral F, McElroy SL, McIntosh AM, McMahon FJ, Melle I, Metspalu A, Mitchell PB, Morken G, Mors O, Mortensen PB, Müller-Myhsok B, Myers RM, Neale BM, Nimgaonkar V, Nordentoft M, Nöthen MM, O'Donovan MC, Oedegaard KJ, Owen MJ, Paciga SA, Pato C, Pato MT, Posthuma D, Ramos-Quiroga JA, Ribasés M, Rietschel M, Rouleau GA, Schalling M, Schofield PR, Schulze TG, Serretti A, Smoller JW, Stefansson H, Stefansson K, Stordal E, Sullivan PF, Turecki G, Vaaler AE, Vieta E, Vincent JB, Werge T, Nurnberger JI, Wray NR, Di Florio A, Edenberg HJ, Cichon S, Ophoff RA, Scott LJ, Andreassen OA, Kelsoe J, Sklar P; Bipolar Disorder Working Group of the Psychiatric Genomics Consortium.

Nat Genet. 2019 May;51(5):793-803. doi: 10.1038/s41588-019-0397-8. Epub 2019 May 1.

PMID:
31043756
3.

Identification of common genetic risk variants for autism spectrum disorder.

Grove J, Ripke S, Als TD, Mattheisen M, Walters RK, Won H, Pallesen J, Agerbo E, Andreassen OA, Anney R, Awashti S, Belliveau R, Bettella F, Buxbaum JD, Bybjerg-Grauholm J, Bækvad-Hansen M, Cerrato F, Chambert K, Christensen JH, Churchhouse C, Dellenvall K, Demontis D, De Rubeis S, Devlin B, Djurovic S, Dumont AL, Goldstein JI, Hansen CS, Hauberg ME, Hollegaard MV, Hope S, Howrigan DP, Huang H, Hultman CM, Klei L, Maller J, Martin J, Martin AR, Moran JL, Nyegaard M, Nærland T, Palmer DS, Palotie A, Pedersen CB, Pedersen MG, dPoterba T, Poulsen JB, Pourcain BS, Qvist P, Rehnström K, Reichenberg A, Reichert J, Robinson EB, Roeder K, Roussos P, Saemundsen E, Sandin S, Satterstrom FK, Davey Smith G, Stefansson H, Steinberg S, Stevens CR, Sullivan PF, Turley P, Walters GB, Xu X; Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium; BUPGEN; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium; 23andMe Research Team, Stefansson K, Geschwind DH, Nordentoft M, Hougaard DM, Werge T, Mors O, Mortensen PB, Neale BM, Daly MJ, Børglum AD.

Nat Genet. 2019 Mar;51(3):431-444. doi: 10.1038/s41588-019-0344-8. Epub 2019 Feb 25.

4.

A new variant (c.1A>G) in LDLRAP1 causing autosomal recessive hypercholesterolemia: Characterization of the defect and response to PCSK9 inhibition.

Rodríguez-Jiménez C, Gómez-Coronado D, Frías Vargas M, Cerrato F, Lahoz C, Saban-Ruiz J, González-Nieto D, Lasunción MA, Mostaza JM, Rodríguez-Nóvoa S.

Atherosclerosis. 2019 May;284:223-229. doi: 10.1016/j.atherosclerosis.2019.01.010. Epub 2019 Jan 25.

PMID:
30777337
5.

Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus.

Valente FM, Sparago A, Freschi A, Hill-Harfe K, Maas SM, Frints SGM, Alders M, Pignata L, Franzese M, Angelini C, Carli D, Mussa A, Gazzin A, Gabbarini F, Acurzio B, Ferrero GB, Bliek J, Williams CA, Riccio A, Cerrato F.

Genet Med. 2019 Aug;21(8):1808-1820. doi: 10.1038/s41436-018-0416-7. Epub 2019 Jan 12.

6.

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.

Demontis D, Walters RK, Martin J, Mattheisen M, Als TD, Agerbo E, Baldursson G, Belliveau R, Bybjerg-Grauholm J, Bækvad-Hansen M, Cerrato F, Chambert K, Churchhouse C, Dumont A, Eriksson N, Gandal M, Goldstein JI, Grasby KL, Grove J, Gudmundsson OO, Hansen CS, Hauberg ME, Hollegaard MV, Howrigan DP, Huang H, Maller JB, Martin AR, Martin NG, Moran J, Pallesen J, Palmer DS, Pedersen CB, Pedersen MG, Poterba T, Poulsen JB, Ripke S, Robinson EB, Satterstrom FK, Stefansson H, Stevens C, Turley P, Walters GB, Won H, Wright MJ; ADHD Working Group of the Psychiatric Genomics Consortium (PGC); Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium; 23andMe Research Team, Andreassen OA, Asherson P, Burton CL, Boomsma DI, Cormand B, Dalsgaard S, Franke B, Gelernter J, Geschwind D, Hakonarson H, Haavik J, Kranzler HR, Kuntsi J, Langley K, Lesch KP, Middeldorp C, Reif A, Rohde LA, Roussos P, Schachar R, Sklar P, Sonuga-Barke EJS, Sullivan PF, Thapar A, Tung JY, Waldman ID, Medland SE, Stefansson K, Nordentoft M, Hougaard DM, Werge T, Mors O, Mortensen PB, Daly MJ, Faraone SV, Børglum AD, Neale BM.

Nat Genet. 2019 Jan;51(1):63-75. doi: 10.1038/s41588-018-0269-7. Epub 2018 Nov 26.

7.

The Effect of Surgical Treatment for Gynecomastia on Quality of Life in Adolescents.

Nuzzi LC, Firriolo JM, Pike CM, Cerrato FE, DiVasta AD, Labow BI.

J Adolesc Health. 2018 Dec;63(6):759-765. doi: 10.1016/j.jadohealth.2018.06.028. Epub 2018 Sep 29.

PMID:
30279103
8.

Is ZFP57 binding to H19/IGF2:IG-DMR affected in Silver-Russell syndrome?

Sparago A, Cerrato F, Riccio A.

Clin Epigenetics. 2018 Feb 21;10:23. doi: 10.1186/s13148-018-0454-7. eCollection 2018.

9.

Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice.

Freschi A, Hur SK, Valente FM, Ideraabdullah FY, Sparago A, Gentile MT, Oneglia A, Di Nucci D, Colucci-D'Amato L, Thorvaldsen JL, Bartolomei MS, Riccio A, Cerrato F.

PLoS Genet. 2018 Feb 22;14(2):e1007243. doi: 10.1371/journal.pgen.1007243. eCollection 2018 Feb.

10.

The Effect of Reduction Mammaplasty on Quality of Life in Adolescents With Macromastia.

Nuzzi LC, Firriolo JM, Pike CM, Cerrato FE, Webb ML, Faulkner HR, DiVasta AD, Labow BI.

Pediatrics. 2017 Nov;140(5). pii: e20171103. doi: 10.1542/peds.2017-1103. Epub 2017 Oct 6.

11.

Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome.

Mussa A, Molinatto C, Cerrato F, Palumbo O, Carella M, Baldassarre G, Carli D, Peris C, Riccio A, Ferrero GB.

Pediatrics. 2017 Jul;140(1). pii: e20164311. doi: 10.1542/peds.2016-4311. Epub 2017 Jun 20.

12.

Never too late to be anxious: validation of the Geriatric Anxiety Inventory, Italian version.

Ferrari S, Signorelli MS, Cerrato F, Pingani L, Massimino M, Valente S, Forlani M, Bonasegla P, Arcidiacono E, De Ronchi D, Rigatelli M, Aguglia E, Atti AR.

Clin Ter. 2017 Mar-Apr;168(2):e120-e127. doi: 10.7417/CT.2017.1992.

13.

Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes.

Hur SK, Freschi A, Ideraabdullah F, Thorvaldsen JL, Luense LJ, Weller AH, Berger SL, Cerrato F, Riccio A, Bartolomei MS.

Proc Natl Acad Sci U S A. 2016 Sep 27;113(39):10938-43. doi: 10.1073/pnas.1603066113. Epub 2016 Sep 12.

14.

Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes.

Boonen SE, Freschi A, Christensen R, Valente FM, Lildballe DL, Perone L, Palumbo O, Carella M, Uldbjerg N, Sparago A, Riccio A, Cerrato F.

Clin Epigenetics. 2016 Jun 16;8:69. doi: 10.1186/s13148-016-0236-z. eCollection 2016.

15.

ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells.

Anvar Z, Cammisa M, Riso V, Baglivo I, Kukreja H, Sparago A, Girardot M, Lad S, De Feis I, Cerrato F, Angelini C, Feil R, Pedone PV, Grimaldi G, Riccio A.

Nucleic Acids Res. 2016 Feb 18;44(3):1118-32. doi: 10.1093/nar/gkv1059. Epub 2015 Oct 19.

16.

A novel large deletion of the ICR1 region including H19 and putative enhancer elements.

Fryssira H, Amenta S, Kanber D, Sofocleous C, Lykopoulou E, Kanaka-Gantenbein C, Cerrato F, Lüdecke HJ, Bens S, Riccio A, Buiting K.

BMC Med Genet. 2015 May 6;16:30. doi: 10.1186/s12881-015-0173-2.

17.

A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype.

De Crescenzo A, Citro V, Freschi A, Sparago A, Palumbo O, Cubellis MV, Carella M, Castelluccio P, Cavaliere ML, Cerrato F, Riccio A.

J Hum Genet. 2015 Jun;60(6):287-93. doi: 10.1038/jhg.2015.29. Epub 2015 Mar 26.

PMID:
25809938
18.

Reply: Psychological Impact of Breast Asymmetry on Adolescents: A Prospective Cohort.

Nuzzi LC, Cerrato FE, Webb ML, Faulkner HR, Walsh EM, DiVasta AD, Greene AK, Labow BI.

Plast Reconstr Surg. 2015 Jul;136(1):109e-110e. doi: 10.1097/PRS.0000000000001342. No abstract available.

PMID:
25803163
19.

Intermediate and Long-term Outcomes of Giant Fibroadenoma Excision in Adolescent and Young Adult Patients.

Cerrato FE, Pruthi S, Boughey JC, Simmons PS, Salje B, Nuzzi LC, Lemaine V, Labow BI.

Breast J. 2015 May-Jun;21(3):254-9. doi: 10.1111/tbj.12394. Epub 2015 Mar 13.

PMID:
25772491
20.

Preoperative electrocardiograms for nonsyndromic children with hand syndactyly.

Nuzzi LC, Pike CM, Lewine EB, Cerrato FE, Alexander ME, Ferrari LR, Bae DS, Taghinia A, Waters PM, Labow BI.

J Hand Surg Am. 2015 Mar;40(3):452-5. doi: 10.1016/j.jhsa.2014.10.053. Epub 2014 Dec 24.

PMID:
25542431
21.

Psychological impact of breast asymmetry on adolescents: a prospective cohort study.

Nuzzi LC, Cerrato FE, Webb ML, Faulkner HR, Walsh EM, DiVasta AD, Greene AK, Labow BI.

Plast Reconstr Surg. 2014 Dec;134(6):1116-23. doi: 10.1097/PRS.0000000000000736.

PMID:
25415081
22.

Clinically used selective oestrogen receptor modulators increase LDL receptor activity in primary human lymphocytes.

Cerrato F, Fernández-Suárez ME, Alonso R, Alonso M, Vázquez C, Pastor O, Mata P, Lasunción MA, Gómez-Coronado D.

Br J Pharmacol. 2015 Mar;172(5):1379-94. doi: 10.1111/bph.13016. Epub 2015 Jan 8.

23.

Upper extremity anomalies in Pfeiffer syndrome and mutational correlations.

Cerrato FE, Nuzzi LC, Theman TA, Taghinia A, Upton J, Labow BI.

Plast Reconstr Surg. 2014 May;133(5):654e-661e. doi: 10.1097/PRS.0000000000000107.

PMID:
24776567
24.

Definition of a multi-criteria, web-based approach to managing the illegal dumping of solid waste in Italian villages.

De Feoa G, Cerrato F, Siano P, Torretta V.

Environ Technol. 2014 Jan-Feb;35(1-4):104-14.

PMID:
24600847
25.

Effects of prolonged wakefulness: the role of PERIOD3 genotypes and personality traits.

Barbato G, Costanzo A, Della Monica C, D'Onofrio P, Cerrato F, De Padova V.

Psychol Rep. 2013 Oct;113(2):540-51.

PMID:
24597447
26.

Looking for CDKN1C enhancers.

Cerrato F, De Crescenzo A, Riccio A.

Eur J Hum Genet. 2014 Apr;22(4):442-3. doi: 10.1038/ejhg.2013.234. Epub 2013 Oct 16. No abstract available.

27.

Presentation and treatment of macrodactyly in children.

Cerrato F, Eberlin KR, Waters P, Upton J, Taghinia A, Labow BI.

J Hand Surg Am. 2013 Nov;38(11):2112-23. doi: 10.1016/j.jhsa.2013.08.095. Epub 2013 Sep 20.

PMID:
24060511
28.

Psychosocial impact of adolescent gynecomastia: a prospective case-control study.

Nuzzi LC, Cerrato FE, Erickson CR, Webb ML, Rosen H, Walsh EM, DiVasta AD, Greene AK, Labow BI.

Plast Reconstr Surg. 2013 Apr;131(4):890-6. doi: 10.1097/PRS.0b013e3182818ea8. Erratum in: Plast Reconstr Surg. 2013 May;131(5):1208. Erikson, Cameron R [corrected to Erickson, Cameron R].

PMID:
23542261
29.

Mutations in KCTD1 cause scalp-ear-nipple syndrome.

Marneros AG, Beck AE, Turner EH, McMillin MJ, Edwards MJ, Field M, de Macena Sobreira NL, Perez AB, Fortes JA, Lampe AK, Giovannucci Uzielli ML, Gordon CT, Plessis G, Le Merrer M, Amiel J, Reichenberger E, Shively KM, Cerrato F, Labow BI, Tabor HK, Smith JD, Shendure J, Nickerson DA, Bamshad MJ; University of Washington Center for Mendelian Genomics.

Am J Hum Genet. 2013 Apr 4;92(4):621-6. doi: 10.1016/j.ajhg.2013.03.002. Epub 2013 Mar 28.

30.

Diagnosis and management of fibroadenomas in the adolescent breast.

Cerrato F, Labow BI.

Semin Plast Surg. 2013 Feb;27(1):23-5. doi: 10.1055/s-0033-1343992.

31.

Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction.

De Crescenzo A, Sparago A, Cerrato F, Palumbo O, Carella M, Miceli M, Bronshtein M, Riccio A, Yaron Y.

J Med Genet. 2013 Feb;50(2):99-103. doi: 10.1136/jmedgenet-2012-101352. Epub 2012 Dec 14.

32.

The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites.

Beygo J, Citro V, Sparago A, De Crescenzo A, Cerrato F, Heitmann M, Rademacher K, Guala A, Enklaar T, Anichini C, Cirillo Silengo M, Graf N, Prawitt D, Cubellis MV, Horsthemke B, Buiting K, Riccio A.

Hum Mol Genet. 2013 Feb 1;22(3):544-57. doi: 10.1093/hmg/dds465. Epub 2012 Oct 30.

33.

Expression analysis of macrodactyly identifies pleiotrophin upregulation.

Lau FH, Xia F, Kaplan A, Cerrato F, Greene AK, Taghinia A, Cowan CA, Labow BI.

PLoS One. 2012;7(7):e40423. doi: 10.1371/journal.pone.0040423. Epub 2012 Jul 27.

34.

The impact of macromastia on adolescents: a cross-sectional study.

Cerrato F, Webb ML, Rosen H, Nuzzi L, McCarty ER, DiVasta AD, Greene AK, Labow BI.

Pediatrics. 2012 Aug;130(2):e339-46. doi: 10.1542/peds.2011-3869. Epub 2012 Jul 16.

PMID:
22802601
35.

Outcomes in pediatric atypical spitz tumors treated without sentinel lymph node biopsy.

Cerrato F, Wallins JS, Webb ML, McCarty ER, Schmidt BA, Labow BI.

Pediatr Dermatol. 2012 Jul-Aug;29(4):448-53. doi: 10.1111/j.1525-1470.2011.01699.x. Epub 2011 Dec 30.

PMID:
22211716
36.

The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases.

Chiesa N, De Crescenzo A, Mishra K, Perone L, Carella M, Palumbo O, Mussa A, Sparago A, Cerrato F, Russo S, Lapi E, Cubellis MV, Kanduri C, Cirillo Silengo M, Riccio A, Ferrero GB.

Hum Mol Genet. 2012 Jan 1;21(1):10-25. doi: 10.1093/hmg/ddr419. Epub 2011 Sep 14.

37.

GnRH-deficient phenotypes in humans and mice with heterozygous variants in KISS1/Kiss1.

Chan YM, Broder-Fingert S, Paraschos S, Lapatto R, Au M, Hughes V, Bianco SD, Min L, Plummer L, Cerrato F, De Guillebon A, Wu IH, Wahab F, Dwyer A, Kirsch S, Quinton R, Cheetham T, Ozata M, Ten S, Chanoine JP, Pitteloud N, Martin KA, Schiffmann R, Van der Kamp HJ, Nader S, Hall JE, Kaiser UB, Seminara SB.

J Clin Endocrinol Metab. 2011 Nov;96(11):E1771-81. doi: 10.1210/jc.2011-0518. Epub 2011 Aug 31.

38.

Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: variant reclassification and surgical decisions.

Murray ML, Cerrato F, Bennett RL, Jarvik GP.

Genet Med. 2011 Dec;13(12):998-1005. doi: 10.1097/GIM.0b013e318226fc15.

PMID:
21811163
39.

The effect of obesity on early outcomes in adolescents undergoing reduction mammaplasty.

Webb ML, Cerrato F, Rosen H, DiVasta AD, Greene AK, Labow BI.

Ann Plast Surg. 2012 Mar;68(3):257-60. doi: 10.1097/SAP.0b013e3182145370.

PMID:
21629095
40.

A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome.

De Crescenzo A, Coppola F, Falco P, Bernardo I, Ausanio G, Cerrato F, Falco L, Riccio A.

Eur J Med Genet. 2011 Jul-Aug;54(4):e451-4. doi: 10.1016/j.ejmg.2011.04.009. Epub 2011 May 4.

41.

Incidence of Fanconi anemia in children with congenital thumb anomalies referred for diepoxybutane testing.

Webb ML, Rosen H, Taghinia A, McCarty ER, Cerrato F, Upton J, Labow BI.

J Hand Surg Am. 2011 Jun;36(6):1052-7. doi: 10.1016/j.jhsa.2011.02.018. Epub 2011 Apr 22.

PMID:
21514743
42.

Genetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk.

Ronald J, Rajagopalan R, Cerrato F, Nord AS, Hatsukami T, Kohler T, Marcovina S, Heagerty P, Jarvik GP.

Stroke. 2011 Jan;42(1):2-9. doi: 10.1161/STROKEAHA.110.591230. Epub 2010 Dec 2.

43.

GNRH1 mutations in patients with idiopathic hypogonadotropic hypogonadism.

Chan YM, de Guillebon A, Lang-Muritano M, Plummer L, Cerrato F, Tsiaras S, Gaspert A, Lavoie HB, Wu CH, Crowley WF Jr, Amory JK, Pitteloud N, Seminara SB.

Proc Natl Acad Sci U S A. 2009 Jul 14;106(28):11703-8. doi: 10.1073/pnas.0903449106. Epub 2009 Jun 30.

44.

Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor.

Riccio A, Sparago A, Verde G, De Crescenzo A, Citro V, Cubellis MV, Ferrero GB, Silengo MC, Russo S, Larizza L, Cerrato F.

Endocr Dev. 2009;14:1-9. doi: 10.1159/000207461. Epub 2009 Feb 27. Review.

PMID:
19293570
45.

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.

Bliek J, Verde G, Callaway J, Maas SM, De Crescenzo A, Sparago A, Cerrato F, Russo S, Ferraiuolo S, Rinaldi MM, Fischetto R, Lalatta F, Giordano L, Ferrari P, Cubellis MV, Larizza L, Temple IK, Mannens MM, Mackay DJ, Riccio A.

Eur J Hum Genet. 2009 May;17(5):611-9. doi: 10.1038/ejhg.2008.233. Epub 2008 Dec 17.

46.

A standard echocardiographic and tissue Doppler study of morphological and functional findings in children with hypertrophic cardiomyopathy compared to those with left ventricular hypertrophy in the setting of Noonan and LEOPARD syndromes.

Cerrato F, Pacileo G, Limongelli G, Gagliardi MG, Santoro G, Digilio MC, Di Salvo G, Ardorisio R, Miele T, Calabrò R.

Cardiol Young. 2008 Dec;18(6):575-80. doi: 10.1017/S104795110800320X. Epub 2008 Oct 9.

PMID:
18842161
47.

High frequency of loss of heterozygosity at 11p15 and IGF2 overexpression are not related to clinical outcome in childhood adrenocortical tumors positive for the R337H TP53 mutation.

Rosati R, Cerrato F, Doghman M, Pianovski MA, Parise GA, Custódio G, Zambetti GP, Ribeiro RC, Riccio A, Figueiredo BC, Lalli E.

Cancer Genet Cytogenet. 2008 Oct;186(1):19-24. doi: 10.1016/j.cancergencyto.2008.05.010.

48.

Comparative effects of dietary supplementation with red grape juice and vitamin E on production of superoxide by circulating neutrophil NADPH oxidase in hemodialysis patients.

Castilla P, Dávalos A, Teruel JL, Cerrato F, Fernández-Lucas M, Merino JL, Sánchez-Martín CC, Ortuño J, Lasunción MA.

Am J Clin Nutr. 2008 Apr;87(4):1053-61.

PMID:
18400731
49.

Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer.

Murrell A, Ito Y, Verde G, Huddleston J, Woodfine K, Silengo MC, Spreafico F, Perotti D, De Crescenzo A, Sparago A, Cerrato F, Riccio A.

PLoS One. 2008 Mar 26;3(3):e1849. doi: 10.1371/journal.pone.0001849.

50.

Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour.

Cerrato F, Sparago A, Verde G, De Crescenzo A, Citro V, Cubellis MV, Rinaldi MM, Boccuto L, Neri G, Magnani C, D'Angelo P, Collini P, Perotti D, Sebastio G, Maher ER, Riccio A.

Hum Mol Genet. 2008 May 15;17(10):1427-35. doi: 10.1093/hmg/ddn031. Epub 2008 Feb 1.

PMID:
18245780

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