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Items: 1 to 50 of 60

1.

Surgical Technique for Endometrioma in 10 Steps.

Bourdel N, Paracchini S, Chauvet P, Fava V, Gałczyński K, Canis M.

J Minim Invasive Gynecol. 2019 Jul 31. pii: S1553-4650(19)30327-9. doi: 10.1016/j.jmig.2019.07.023. [Epub ahead of print]

PMID:
31376583
2.

A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism.

Diquigiovanni C, Bergamini C, Diaz R, Liparulo I, Bianco F, Masin L, Baldassarro VA, Rizzardi N, Tranchina A, Buscherini F, Wischmeijer A, Pippucci T, Scarano E, Cordelli DM, Fato R, Seri M, Paracchini S, Bonora E.

FASEB J. 2019 Oct;33(10):11284-11302. doi: 10.1096/fj.201802722R. Epub 2019 Aug 7.

PMID:
31314595
3.

Genomic Imprinting As a Window into Human Language Evolution.

Hitchcock TJ, Paracchini S, Gardner A.

Bioessays. 2019 Jun;41(6):e1800212. doi: 10.1002/bies.201800212. Review.

PMID:
31132171
4.

Laparoscopic Ovarian Dermoid Cystectomy in 10 Steps.

Paracchini S, Rhazi Y, Chauvet P, Gałczyński K, Jaillet L, Canis M, Bourdel N.

J Minim Invasive Gynecol. 2019 May 22. pii: S1553-4650(19)30222-5. doi: 10.1016/j.jmig.2019.05.009. [Epub ahead of print]

PMID:
31125721
5.

Comparison of two "a priori" risk assessment algorithms for preeclampsia in Italy: a prospective multicenter study.

Di Martino D, Masturzo B, Paracchini S, Bracco B, Cavoretto P, Prefumo F, Germano C, Morano D, Girlando F, Giorgione V, Parpinel G, Cariello L, Fusè F, Candiani M, Todros T, Rizzo N, Farina A.

Arch Gynecol Obstet. 2019 Jun;299(6):1587-1596. doi: 10.1007/s00404-019-05146-4. Epub 2019 Apr 5.

PMID:
30953193
6.

The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migration.

Gostic M, Martinelli A, Tucker C, Yang Z, Gasparoli F, Ewart JY, Dholakia K, Sillar KT, Tello JA, Paracchini S.

J Comp Neurol. 2019 Nov 1;527(16):2634-2643. doi: 10.1002/cne.24696. Epub 2019 Apr 16.

7.

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.

Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, St Pourcain B, Brandler W, Honbolygó F, Tóth D, Csépe V, Huguet G, Morris AP, Hulslander J, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Vaessen A, Maurer U, Lyytinen H, Peyrard-Janvid M, Leppänen PHT, Brandeis D, Bonte M, Stein JF, Talcott JB, Fauchereau F, Wilcke A, Francks C, Bourgeron T, Monaco AP, Ramus F, Landerl K, Kere J, Scerri TS, Paracchini S, Fisher SE, Schumacher J, Nöthen MM, Müller-Myhsok B, Schulte-Körne G.

Transl Psychiatry. 2019 Feb 11;9(1):77. doi: 10.1038/s41398-019-0402-0.

8.

Impact of cancer in the management of delivery: 10 years of variations.

Masturzo B, Parpinel G, Macchi C, De Ruvo D, Paracchini S, Baima Poma C, Danna P, Pagliardini G, Zola P.

J Matern Fetal Neonatal Med. 2018 Dec 20:1-6. doi: 10.1080/14767058.2018.1536117. [Epub ahead of print]

PMID:
30572764
9.

The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on.

Guidi LG, Velayos-Baeza A, Martinez-Garay I, Monaco AP, Paracchini S, Bishop DVM, Molnár Z.

Eur J Neurosci. 2018 Nov;48(10):3212-3233. doi: 10.1111/ejn.14149. Epub 2018 Oct 6. Review.

10.

Upcoming strategies in obstetrics: how the technology of clinical audit may reduce cesarean birth.

Paracchini S, Masturzo B, Tangolo D, Roletti E, Piazzese A, Attini R, Rolfo A, Todros T.

Minerva Ginecol. 2017 Dec;69(6):548-554. doi: 10.23736/S0026-4784.17.04035-7.

PMID:
29082725
11.

The DCDC2 deletion is not a risk factor for dyslexia.

Scerri TS, Macpherson E, Martinelli A, Wa WC, Monaco AP, Stein J, Zheng M, Suk-Han Ho C, McBride C, Snowling M, Hulme C, Hayiou-Thomas ME, Waye MMY, Talcott JB, Paracchini S.

Transl Psychiatry. 2017 Jul 25;7(7):e1182. doi: 10.1038/tp.2017.151.

12.

Time remaining in labor and probability of vaginal delivery as a function of the angle of progression in a low risk population with a normal first stage of labor. In-house observational study and comparison with the data in the literature.

Masturzo B, Piazzese A, Paracchini S, Quezada MS, Todros T, Farina A.

Minerva Ginecol. 2018 Feb;70(1):35-43. doi: 10.23736/S0026-4784.17.04091-6. Epub 2017 Jun 7.

PMID:
28590104
13.

Advances in Dyslexia Genetics-New Insights Into the Role of Brain Asymmetries.

Paracchini S, Diaz R, Stein J.

Adv Genet. 2016;96:53-97. doi: 10.1016/bs.adgen.2016.08.003. Epub 2016 Oct 5. Review.

PMID:
27968731
14.

Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.

Pettigrew KA, Frinton E, Nudel R, Chan MTM, Thompson P, Hayiou-Thomas ME, Talcott JB, Stein J, Monaco AP, Hulme C, Snowling MJ, Newbury DF, Paracchini S.

J Neurodev Disord. 2016 Jun 14;8:24. doi: 10.1186/s11689-016-9157-6. eCollection 2016.

15.

The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts.

Shore R, Covill L, Pettigrew KA, Brandler WM, Diaz R, Xu Y, Tello JA, Talcott JB, Newbury DF, Stein J, Monaco AP, Paracchini S.

Hum Mol Genet. 2016 May 1;25(9):1771-9. doi: 10.1093/hmg/ddw047. Epub 2016 Feb 21.

16.

Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.

Pettigrew KA, Reeves E, Leavett R, Hayiou-Thomas ME, Sharma A, Simpson NH, Martinelli A, Thompson P, Hulme C, Snowling MJ, Newbury DF, Paracchini S.

PLoS One. 2015 Aug 11;10(8):e0134997. doi: 10.1371/journal.pone.0134997. eCollection 2015.

17.

Lack of replication for the myosin-18B association with mathematical ability in independent cohorts.

Pettigrew KA, Fajutrao Valles SF, Moll K, Northstone K, Ring S, Pennell C, Wang C, Leavett R, Hayiou-Thomas ME, Thompson P, Simpson NH, Fisher SE; SLI Consortium, Whitehouse AJ, Snowling MJ, Newbury DF, Paracchini S.

Genes Brain Behav. 2015 Apr;14(4):369-76. doi: 10.1111/gbb.12213. Epub 2015 Apr 1.

18.

Genome-wide screening for DNA variants associated with reading and language traits.

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.

Genes Brain Behav. 2014 Sep;13(7):686-701. doi: 10.1111/gbb.12158. Epub 2014 Aug 29.

19.

Reading and language disorders: the importance of both quantity and quality.

Newbury DF, Monaco AP, Paracchini S.

Genes (Basel). 2014 Apr 4;5(2):285-309. doi: 10.3390/genes5020285.

20.

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.

Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER; SLI Consortium, Ring SM, Davey Smith G, Francks C, Paracchini S, Monaco AP, Fisher SE, Newbury DF.

Genes Brain Behav. 2014 Apr;13(4):418-29. doi: 10.1111/gbb.12127. Epub 2014 Mar 24.

21.

Isoflavone content and estrogenic activity of different batches of red clover (Trifolium pratense L.) extracts: an in vitro study in MCF-7 cells.

Spagnuolo P, Rasini E, Luini A, Legnaro M, Luzzani M, Casareto E, Carreri M, Paracchini S, Marino F, Cosentino M.

Fitoterapia. 2014 Apr;94:62-9. doi: 10.1016/j.fitote.2014.01.027. Epub 2014 Feb 5.

PMID:
24508860
22.

The genetic relationship between handedness and neurodevelopmental disorders.

Brandler WM, Paracchini S.

Trends Mol Med. 2014 Feb;20(2):83-90. doi: 10.1016/j.molmed.2013.10.008. Epub 2013 Nov 23. Review.

23.

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.

Simpson NH, Addis L, Brandler WM, Slonims V, Clark A, Watson J, Scerri TS, Hennessy ER, Bolton PF, Conti-Ramsden G, Fairfax BP, Knight JC, Stein J, Talcott JB, O'Hare A, Baird G, Paracchini S, Fisher SE, Newbury DF; SLI Consortium.

Dev Med Child Neurol. 2014 Apr;56(4):346-53. doi: 10.1111/dmcn.12294. Epub 2013 Oct 9.

24.

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.

Brandler WM, Morris AP, Evans DM, Scerri TS, Kemp JP, Timpson NJ, St Pourcain B, Smith GD, Ring SM, Stein J, Monaco AP, Talcott JB, Fisher SE, Webber C, Paracchini S.

PLoS Genet. 2013;9(9):e1003751. doi: 10.1371/journal.pgen.1003751. Epub 2013 Sep 12.

25.

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.

Becker J, Czamara D, Scerri TS, Ramus F, Csépe V, Talcott JB, Stein J, Morris A, Ludwig KU, Hoffmann P, Honbolygó F, Tóth D, Fauchereau F, Bogliotti C, Iannuzzi S, Chaix Y, Valdois S, Billard C, George F, Soares-Boucaud I, Gérard CL, van der Mark S, Schulz E, Vaessen A, Maurer U, Lohvansuu K, Lyytinen H, Zucchelli M, Brandeis D, Blomert L, Leppänen PH, Bruder J, Monaco AP, Müller-Myhsok B, Kere J, Landerl K, Nöthen MM, Schulte-Körne G, Paracchini S, Peyrard-Janvid M, Schumacher J.

Eur J Hum Genet. 2014 May;22(5):675-80. doi: 10.1038/ejhg.2013.199. Epub 2013 Sep 11.

26.

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.

Scerri TS, Darki F, Newbury DF, Whitehouse AJ, Peyrard-Janvid M, Matsson H, Ang QW, Pennell CE, Ring S, Stein J, Morris AP, Monaco AP, Kere J, Talcott JB, Klingberg T, Paracchini S.

PLoS One. 2012;7(11):e50321. doi: 10.1371/journal.pone.0050321. Epub 2012 Nov 28.

27.

Dissection of genetic associations with language-related traits in population-based cohorts.

Paracchini S.

J Neurodev Disord. 2011 Dec;3(4):365-73. doi: 10.1007/s11689-011-9091-6. Epub 2011 Sep 6.

28.

DCDC2, KIAA0319 and CMIP are associated with reading-related traits.

Scerri TS, Morris AP, Buckingham LL, Newbury DF, Miller LL, Monaco AP, Bishop DV, Paracchini S.

Biol Psychiatry. 2011 Aug 1;70(3):237-45. doi: 10.1016/j.biopsych.2011.02.005. Epub 2011 Mar 31.

29.

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.

Newbury DF, Paracchini S, Scerri TS, Winchester L, Addis L, Richardson AJ, Walter J, Stein JF, Talcott JB, Monaco AP.

Behav Genet. 2011 Jan;41(1):90-104. doi: 10.1007/s10519-010-9424-3. Epub 2010 Dec 17.

30.

An allele-specific gene expression assay to test the functional basis of genetic associations.

Paracchini S, Monaco AP, Knight JC.

J Vis Exp. 2010 Nov 3;(45). pii: 2279. doi: 10.3791/2279.

31.

Identification of candidate genes for dyslexia susceptibility on chromosome 18.

Scerri TS, Paracchini S, Morris A, MacPhie IL, Talcott J, Stein J, Smith SD, Pennington BF, Olson RK, DeFries JC, Monaco AP, Richardson AJ.

PLoS One. 2010 Oct 28;5(10):e13712. doi: 10.1371/journal.pone.0013712. Erratum in: PLoS One. 2010;5(12). doi: 10.1371/annotation/2294a38b-878d-42f0-9faf-0822db4a0248. Richardson, Alex J [added].

32.

PCSK6 is associated with handedness in individuals with dyslexia.

Scerri TS, Brandler WM, Paracchini S, Morris AP, Ring SM, Richardson AJ, Talcott JB, Stein J, Monaco AP.

Hum Mol Genet. 2011 Feb 1;20(3):608-14. doi: 10.1093/hmg/ddq475. Epub 2010 Nov 4.

33.

Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.

Paracchini S, Ang QW, Stanley FJ, Monaco AP, Pennell CE, Whitehouse AJ.

Genes Brain Behav. 2011 Mar;10(2):158-65. doi: 10.1111/j.1601-183X.2010.00651.x. Epub 2010 Oct 19.

34.

Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.

Pagnamenta AT, Bacchelli E, de Jonge MV, Mirza G, Scerri TS, Minopoli F, Chiocchetti A, Ludwig KU, Hoffmann P, Paracchini S, Lowy E, Harold DH, Chapman JA, Klauck SM, Poustka F, Houben RH, Staal WG, Ophoff RA, O'Donovan MC, Williams J, Nöthen MM, Schulte-Körne G, Deloukas P, Ragoussis J, Bailey AJ, Maestrini E, Monaco AP; International Molecular Genetic Study Of Autism Consortium.

Biol Psychiatry. 2010 Aug 15;68(4):320-8. doi: 10.1016/j.biopsych.2010.02.002. Epub 2010 Mar 26.

35.

Immunomodulatory activity of the lignan 7-hydroxymatairesinol potassium acetate (HMR/lignan) extracted from the heartwood of Norway spruce (Picea abies).

Cosentino M, Marino F, Maio RC, Delle Canne MG, Luzzani M, Paracchini S, Lecchini S.

Int Immunopharmacol. 2010 Mar;10(3):339-43. doi: 10.1016/j.intimp.2009.12.005. Epub 2009 Dec 11.

PMID:
20005303
36.

CMIP and ATP2C2 modulate phonological short-term memory in language impairment.

Newbury DF, Winchester L, Addis L, Paracchini S, Buckingham LL, Clark A, Cohen W, Cowie H, Dworzynski K, Everitt A, Goodyer IM, Hennessy E, Kindley AD, Miller LL, Nasir J, O'Hare A, Shaw D, Simkin Z, Simonoff E, Slonims V, Watson J, Ragoussis J, Fisher SE, Seckl JR, Helms PJ, Bolton PF, Pickles A, Conti-Ramsden G, Baird G, Bishop DV, Monaco AP.

Am J Hum Genet. 2009 Aug;85(2):264-72. doi: 10.1016/j.ajhg.2009.07.004. Epub 2009 Jul 30.

37.

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.

Dennis MY, Paracchini S, Scerri TS, Prokunina-Olsson L, Knight JC, Wade-Martins R, Coggill P, Beck S, Green ED, Monaco AP.

PLoS Genet. 2009 Mar;5(3):e1000436. doi: 10.1371/journal.pgen.1000436. Epub 2009 Mar 27.

38.

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.

Paracchini S, Steer CD, Buckingham LL, Morris AP, Ring S, Scerri T, Stein J, Pembrey ME, Ragoussis J, Golding J, Monaco AP.

Am J Psychiatry. 2008 Dec;165(12):1576-84. doi: 10.1176/appi.ajp.2008.07121872. Epub 2008 Oct 1.

PMID:
18829873
39.

The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms.

Velayos-Baeza A, Toma C, Paracchini S, Monaco AP.

Hum Mol Genet. 2008 Mar 15;17(6):859-71. Epub 2007 Dec 6.

PMID:
18063668
40.

Alternative splicing in the dyslexia-associated gene KIAA0319.

Velayos-Baeza A, Toma C, da Roza S, Paracchini S, Monaco AP.

Mamm Genome. 2007 Sep;18(9):627-34. Epub 2007 Sep 11.

PMID:
17846832
41.

Estrogenic activity of 7-hydroxymatairesinol potassium acetate (HMR/lignan) from Norway spruce (Picea abies) knots and of its active metabolite enterolactone in MCF-7 cells.

Cosentino M, Marino F, Ferrari M, Rasini E, Bombelli R, Luini A, Legnaro M, Delle Canne MG, Luzzani M, Crema F, Paracchini S, Lecchini S.

Pharmacol Res. 2007 Aug;56(2):140-7. Epub 2007 May 22.

PMID:
17572100
42.

The genetic lexicon of dyslexia.

Paracchini S, Scerri T, Monaco AP.

Annu Rev Genomics Hum Genet. 2007;8:57-79. Review.

PMID:
17444811
43.

Haplotype-specific expression of exon 10 at the human MAPT locus.

Caffrey TM, Joachim C, Paracchini S, Esiri MM, Wade-Martins R.

Hum Mol Genet. 2006 Dec 15;15(24):3529-37. Epub 2006 Nov 3.

PMID:
17085483
44.

Y-chromosomal insights into the genetic impact of the caste system in India.

Zerjal T, Pandya A, Thangaraj K, Ling EY, Kearley J, Bertoneri S, Paracchini S, Singh L, Tyler-Smith C.

Hum Genet. 2007 Mar;121(1):137-44. Epub 2006 Oct 31.

45.

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.

Harold D, Paracchini S, Scerri T, Dennis M, Cope N, Hill G, Moskvina V, Walter J, Richardson AJ, Owen MJ, Stein JF, Green ED, O'Donovan MC, Williams J, Monaco AP.

Mol Psychiatry. 2006 Dec;11(12):1085-91, 1061. Epub 2006 Oct 10.

PMID:
17033633
46.

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.

Paracchini S, Thomas A, Castro S, Lai C, Paramasivam M, Wang Y, Keating BJ, Taylor JM, Hacking DF, Scerri T, Francks C, Richardson AJ, Wade-Martins R, Stein JF, Knight JC, Copp AJ, Loturco J, Monaco AP.

Hum Mol Genet. 2006 May 15;15(10):1659-66. Epub 2006 Apr 6.

PMID:
16600991
47.

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK.

Scerri TS, Fisher SE, Francks C, MacPhie IL, Paracchini S, Richardson AJ, Stein JF, Monaco AP.

J Med Genet. 2004 Nov;41(11):853-7. No abstract available.

48.

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.

Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, Cardon LR, Marlow AJ, MacPhie IL, Walter J, Pennington BF, Fisher SE, Olson RK, DeFries JC, Stein JF, Monaco AP.

Am J Hum Genet. 2004 Dec;75(6):1046-58. Epub 2004 Oct 22.

49.

A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa.

Arredi B, Poloni ES, Paracchini S, Zerjal T, Fathallah DM, Makrelouf M, Pascali VL, Novelletto A, Tyler-Smith C.

Am J Hum Genet. 2004 Aug;75(2):338-45. Epub 2004 Jun 16.

50.

A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N.

Fernandes S, Paracchini S, Meyer LH, Floridia G, Tyler-Smith C, Vogt PH.

Am J Hum Genet. 2004 Jan;74(1):180-7. Epub 2003 Nov 21.

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