Developmental Delay Publications

Publications in Developmental Delay

Explore the most influential research papers and scholarly works that have shaped Developmental Delay. Use the concept filter below to focus on a specific sub-area of research.

Developmental Delay

2.4K

Publications

181K

Citations

Showing yearly statistics from 2000-2026.

Page 1

	Year	Citations
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome Annemieke J.M.H. Verkerk, Maura Pieretti, James S. Sutcliffe, Cell Breakpoint Cluster RegionFragile X SyndromeMendelian DisorderGenetic DisorderGenetics	1991	3.5K
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism Stéphane Jamain, Hélène Quach, Catalina Betancur, Nature Genetics Neurodevelopmental DisordersMolecular NeuroscienceSyndromic AutismGenetic DisorderGenetics	2003	1.8K
Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome I. Oberlé, F. Rousseau, Dominique Heitz, Science Phenotypic ExpressionEpigenetic ChangeGeneticsMolecular BiologyEpigenetics	1991	1.5K
Absence of expression of the FMR-1 gene in fragile X syndrome Maura Pieretti, F Zhang, Ying‐Hui Fu, Cell Fragile X SyndromeDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	1991	1.5K
A copy number variation morbidity map of developmental delay Gregory M. Cooper, Bradley P. Coe, Santhosh Girirajan, Nature Genetics MedicineGeneticsCognitive DevelopmentGlobal Developmental DelayDevelopmental Psychology	2011	1.4K
Altered synaptic plasticity in a mouse model of fragile X mental retardation Kimberly M. Huber, Sean Gallagher, Stephen T. Warren, Proceedings of the National Academy of Sciences Developmental Cognitive NeuroscienceSynaptic TransmissionNeurotransmitterStructural PlasticitySocial Sciences	2002	1.3K
Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X Syndrome Victoria Brown, Peng Jin, Stephanie Ceman, Cell Fragile X SyndromeGenetic DisorderGeneticsFmrp-associated Brain MrnasFragile X Spectrum	2001	1.1K
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, The Lancet Genetic MutationsMendelian DisorderGenetic DisorderGeneticsFragile X Spectrum	2012	1.1K
Fmr1 knockout mice: A model to study fragile X mental retardation Cell Knockout MouseMolecular NeurosciencePsychiatryGenetic DisorderGenetics	1994	1K
Correction of Fragile X Syndrome in Mice Gül Dölen, Emily K. Osterweil, B.S. Shankaranarayana Rao, Neuron Knockout MouseFragile X SyndromeMendelian DisorderGenetic DisorderGenetics	2007	970
Fragile X Mental Retardation Protein Targets G Quartet mRNAs Important for Neuronal Function Jennifer C. Darnell, Kirk B. Jensen, Peng Jin, Cell Molecular NeuroscienceDevelopmental BiologyGenetic DisorderGeneticsFragile X Spectrum	2001	943
Fragile X Genotype Characterized by an Unstable Region of DNA Shuancang Yu, Melanie Pritchard, Eric J. Kremer, Science CytogeneticsFragile X GenotypeGeneticsMolecular BiologyMolecular Genetics	1991	796

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