Dianne F. Newbury - Concepedia

Author

Dianne F. Newbury

Also Known As

, D F Newbury, D. F. Newbury, D.F. Newbury, DIANNE NEWBURY, Dianne F Newbury, Dianne F. Newbury, Dianne Newbury, Newbury, D., Newbury, DF

118

Publications

4.9K

Citations

H-Index

Concepts

All Affiliations

University of Oxford Centre for Human Genetics Oxford Brookes University Radboud University Nijmegen Max Planck Institute for Psycholinguistics

About

Dianne F. Newbury is an author at University of Oxford specializing in genetics, medicine, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	694
2	Social Sciences	6	6	647
3	Language Studies	3	3	93
4	Health Sciences	2	2	59
5	Cognitive Science	2	2	55

Dianne F. Newbury

Publications

3.8K

Citations

H-Index

Page 1

	Year	Citations
A Functional Genetic Link between Distinct Developmental Language Disorders Sonja C. Vernes, Dianne F. Newbury, Brett S. Abrahams, New England Journal of Medicine	2008	684
A Genomewide Scan for Loci Involved in Attention-Deficit/Hyperactivity Disorder Simon E. Fisher, Clyde Francks, James T. McCracken, The American Journal of Human Genetics AdhdPsychiatryPsychiatric GeneticsNeuroscienceDisease Gene Identification	2002	293
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia Simon E. Fisher, Clyde Francks, Angela J. Marlow, Nature Genetics Genetic DisorderGeneticsChromosome 18NeuroscienceNeurology	2001	270
Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects Dianne F. Newbury, Silvia Paracchini, Tom S. Scerri, Behavior Genetics	2010	227
FOXP2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment Dianne F. Newbury, Enzo Bonora, Janine A. Lamb, The American Journal of Human Genetics Neurodevelopmental DisordersSpecific Language ImpairmentMajor Susceptibility GeneSyndromic AutismGenetic Disorder	2002	216
CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment Dianne F. Newbury, Laura Winchester, Laura Addis, The American Journal of Human Genetics	2009	191
DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits Tom S. Scerri, Andrew P. Morris, Lyn-Louise Buckingham, Biological Psychiatry	2011	181
Discovery of 42 genome-wide significant loci associated with dyslexia Catherine Doust, Pierre Fontanillas, Else Eising, Nature Genetics	2022	134
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people Else Eising, Nazanin Mirza‐Schreiber, Eveline L. de Zeeuw, Proceedings of the National Academy of Sciences	2022	126
Genome‐wide screening for <scp>DNA</scp> variants associated with reading and language traits Alessandro Gialluisi, Dianne F. Newbury, E. G. Wilcutt, Genes Brain & Behavior	2014	123

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