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Items: 20

1.

Language deficits in specific language impairment, attention deficit/hyperactivity disorder, and autism spectrum disorder: An analysis of polygenic risk.

Nudel R, Christiani CAJ, Ohland J, Uddin MJ, Hemager N, Ellersgaard DV, Spang KS, Burton BK, Greve AN, Gantriis DL, Bybjerg-Grauholm J, Jepsen JRM, Thorup AAE, Mors O, Nordentoft M, Werge T.

Autism Res. 2019 Oct 2. doi: 10.1002/aur.2211. [Epub ahead of print]

PMID:
31577390
2.

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration.

Liu X, Helenius D, Skotte L, Beaumont RN, Wielscher M, Geller F, Juodakis J, Mahajan A, Bradfield JP, Lin FTJ, Vogelezang S, Bustamante M, Ahluwalia TS, Pitkänen N, Wang CA, Bacelis J, Borges MC, Zhang G, Bedell BA, Rossi RM, Skogstrand K, Peng S, Thompson WK, Appadurai V, Lawlor DA, Kalliala I, Power C, McCarthy MI, Boyd HA, Marazita ML, Hakonarson H, Hayes MG, Scholtens DM, Rivadeneira F, Jaddoe VWV, Vinding RK, Bisgaard H, Knight BA, Pahkala K, Raitakari O, Helgeland Ø, Johansson S, Njølstad PR, Fadista J, Schork AJ, Nudel R, Miller DE, Chen X, Weirauch MT, Mortensen PB, Børglum AD, Nordentoft M, Mors O, Hao K, Ryckman KK, Hougaard DM, Kottyan LC, Pennell CE, Lyytikainen LP, Bønnelykke K, Vrijheid M, Felix JF, Lowe WL Jr, Grant SFA, Hyppönen E, Jacobsson B, Jarvelin MR, Muglia LJ, Murray JC, Freathy RM, Werge TM, Melbye M, Buil A, Feenstra B.

Nat Commun. 2019 Sep 2;10(1):3927. doi: 10.1038/s41467-019-11881-8.

3.

Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorders.

Nudel R, Benros ME, Krebs MD, Allesøe RL, Lemvigh CK, Bybjerg-Grauholm J, Børglum AD, Daly MJ, Nordentoft M, Mors O, Hougaard DM, Mortensen PB, Buil A, Werge T, Rasmussen S, Thompson WK.

Eur J Hum Genet. 2019 Sep;27(9):1445-1455. doi: 10.1038/s41431-019-0402-9. Epub 2019 Apr 11.

4.

A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment.

Schork AJ, Won H, Appadurai V, Nudel R, Gandal M, Delaneau O, Revsbech Christiansen M, Hougaard DM, Bækved-Hansen M, Bybjerg-Grauholm J, Giørtz Pedersen M, Agerbo E, Bøcker Pedersen C, Neale BM, Daly MJ, Wray NR, Nordentoft M, Mors O, Børglum AD, Bo Mortensen P, Buil A, Thompson WK, Geschwind DH, Werge T.

Nat Neurosci. 2019 Mar;22(3):353-361. doi: 10.1038/s41593-018-0320-0. Epub 2019 Jan 28.

5.

Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study.

Erlangsen A, Appadurai V, Wang Y, Turecki G, Mors O, Werge T, Mortensen PB, Starnawska A, Børglum AD, Schork A, Nudel R, Bækvad-Hansen M, Bybjerg-Grauholm J, Hougaard DM, Thompson WK, Nordentoft M, Agerbo E.

Mol Psychiatry. 2018 Aug 16. doi: 10.1038/s41380-018-0218-y. [Epub ahead of print]

PMID:
30116032
6.

Rational confederation of genes and diseases: NGS interpretation via GeneCards, MalaCards and VarElect.

Rappaport N, Fishilevich S, Nudel R, Twik M, Belinky F, Plaschkes I, Stein TI, Cohen D, Oz-Levi D, Safran M, Lancet D.

Biomed Eng Online. 2017 Aug 18;16(Suppl 1):72. doi: 10.1186/s12938-017-0359-2.

7.

GeneHancer: genome-wide integration of enhancers and target genes in GeneCards.

Fishilevich S, Nudel R, Rappaport N, Hadar R, Plaschkes I, Iny Stein T, Rosen N, Kohn A, Twik M, Safran M, Lancet D, Cohen D.

Database (Oxford). 2017 Jan 1;2017. doi: 10.1093/database/bax028.

8.

MalaCards: an amalgamated human disease compendium with diverse clinical and genetic annotation and structured search.

Rappaport N, Twik M, Plaschkes I, Nudel R, Iny Stein T, Levitt J, Gershoni M, Morrey CP, Safran M, Lancet D.

Nucleic Acids Res. 2017 Jan 4;45(D1):D877-D887. doi: 10.1093/nar/gkw1012. Epub 2016 Nov 28. Review.

9.

VarElect: the phenotype-based variation prioritizer of the GeneCards Suite.

Stelzer G, Plaschkes I, Oz-Levi D, Alkelai A, Olender T, Zimmerman S, Twik M, Belinky F, Fishilevich S, Nudel R, Guan-Golan Y, Warshawsky D, Dahary D, Kohn A, Mazor Y, Kaplan S, Iny Stein T, Baris HN, Rappaport N, Safran M, Lancet D.

BMC Genomics. 2016 Jun 23;17 Suppl 2:444. doi: 10.1186/s12864-016-2722-2.

10.

The GeneCards Suite: From Gene Data Mining to Disease Genome Sequence Analyses.

Stelzer G, Rosen N, Plaschkes I, Zimmerman S, Twik M, Fishilevich S, Stein TI, Nudel R, Lieder I, Mazor Y, Kaplan S, Dahary D, Warshawsky D, Guan-Golan Y, Kohn A, Rappaport N, Safran M, Lancet D.

Curr Protoc Bioinformatics. 2016 Jun 20;54:1.30.1-1.30.33. doi: 10.1002/cpbi.5.

PMID:
27322403
11.

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.

12.

An investigation of NFXL1, a gene implicated in a study of specific language impairment.

Nudel R.

J Neurodev Disord. 2016 Apr 5;8:13. doi: 10.1186/s11689-016-9146-9. eCollection 2016.

13.

Increased Power for Detection of Parent-of-Origin Effects via the Use of Haplotype Estimation.

Howey R, Mamasoula C, Töpf A, Nudel R, Goodship JA, Keavney BD, Cordell HJ.

Am J Hum Genet. 2015 Sep 3;97(3):419-34. doi: 10.1016/j.ajhg.2015.07.016. Epub 2015 Aug 27.

14.

Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment.

Villanueva P, Nudel R, Hoischen A, Fernández MA, Simpson NH, Gilissen C, Reader RH, Jara L, Magdalena Echeverry M, Francks C, Baird G, Conti-Ramsden G, O'Hare A, Bolton PF, Hennessy ER; SLI Consortium, Palomino H, Carvajal-Carmona L, Veltman JA, Cazier JB, De Barbieri Z, Fisher SE, Newbury DF.

PLoS Genet. 2015 Jun 26;11(6):e1005336. doi: 10.1371/journal.pgen.1005336. eCollection 2015 Jun. No abstract available.

15.

Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2.

Moralli D, Nudel R, Chan MT, Green CM, Volpi EV, Benítez-Burraco A, Newbury DF, García-Bellido P.

Mol Cytogenet. 2015 Jun 10;8:36. doi: 10.1186/s13039-015-0148-1. eCollection 2015.

16.

Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.

Villanueva P, Nudel R, Hoischen A, Fernández MA, Simpson NH, Gilissen C, Reader RH, Jara L, Echeverry MM, Francks C, Baird G, Conti-Ramsden G, O'Hare A, Bolton PF, Hennessy ER; SLI Consortium, Palomino H, Carvajal-Carmona L, Veltman JA, Cazier JB, De Barbieri Z, Fisher SE, Newbury DF.

PLoS Genet. 2015 Mar 17;11(3):e1004925. doi: 10.1371/journal.pgen.1004925. eCollection 2015 Mar. Erratum in: PLoS Genet. 2015 Jun;11(6):e1005336. Echeverry, Maria Magdalena [corrected to Echeverry, María Magdalena].

17.

Genome-Wide Studies of Specific Language Impairment.

Reader RH, Covill LE, Nudel R, Newbury DF.

Curr Behav Neurosci Rep. 2014;1(4):242-250. Review.

18.

FOXP2.

Nudel R, Newbury DF.

Wiley Interdiscip Rev Cogn Sci. 2013 Sep;4(5):547-560. doi: 10.1002/wcs.1247. Epub 2013 Aug 13. Review.

19.

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.

20.

Associations of HLA alleles with specific language impairment.

Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER; SLI Consortium, Monaco AP, Knight JC, Winney B, Fisher SE, Newbury DF.

J Neurodev Disord. 2014 Jan 17;6(1):1. doi: 10.1186/1866-1955-6-1.

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