Publications by authors named "Ron Nudel"

23Publications

Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders - Findings from a Danish population-based study.

Brain Behav Immun 2020 Jun 11. Epub 2020 Jun 11.

CORE-Copenhagen Research Centre for Mental Health, Mental Health Centre Copenhagen, Copenhagen University Hospital, Copenhagen, Denmark; Department of Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark. Electronic address:

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http://dx.doi.org/10.1016/j.bbi.2020.06.014DOI Listing
June 2020

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

Nat Commun 2019 09 2;10(1):3927. Epub 2019 Sep 2.

Department of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.

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http://dx.doi.org/10.1038/s41467-019-11881-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718389PMC
September 2019

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

Nucleic Acids Res 2017 01 28;45(D1):D877-D887. Epub 2016 Nov 28.

Department of Molecular Genetics, the Weizmann Institute of Science, Rehovot, 76100, Israel

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http://dx.doi.org/10.1093/nar/gkw1012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210521PMC
January 2017

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

Authors:
Ron Nudel

J Neurodev Disord 2016 5;8:13. Epub 2016 Apr 5.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN UK.

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http://dx.doi.org/10.1186/s11689-016-9146-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4822306PMC
April 2016

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

Am J Hum Genet 2015 Sep 27;97(3):419-34. Epub 2015 Aug 27.

Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, NE1 3BZ, UK. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2015.07.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4564992PMC
September 2015

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

Mol Cytogenet 2015 10;8:36. Epub 2015 Jun 10.

Faculty of Linguistics, Philology and Phonetics, University of Oxford, Walton Street, Oxford, OX1 2HG UK ; Faculty of Modern languages, University of Oxford, 47 Wellington Square, Oxford, OX1 2JF UK.

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http://dx.doi.org/10.1186/s13039-015-0148-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460787PMC
June 2015

Genome-Wide Studies of Specific Language Impairment.

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

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN UK ; St John's College, University of Oxford, Oxford, OX1 3JP UK.

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http://dx.doi.org/10.1007/s40473-014-0024-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228195PMC
January 2014

FOXP2.

Wiley Interdiscip Rev Cogn Sci 2013 Sep 13;4(5):547-560. Epub 2013 Aug 13.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.1002/wcs.1247DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992897PMC
September 2013