| scholarly article | Q13442814 |
| P50 | author | Stephen W. Scherer | Q7610775 |
| James F. Gusella | Q1602688 | ||
| Gustavo Turecki | Q3121397 | ||
| Patrick F. Sullivan | Q56249782 | ||
| Fabrice Jollant | Q56748302 | ||
| Cynthia Morton | Q57471012 | ||
| Gilles Maussion | Q60533242 | ||
| Christina M. Hultman | Q65824971 | ||
| Christian Marshall | Q89518827 | ||
| Lisa G Shaffer | Q91772223 | ||
| Sébastien Jacquemont | Q92881209 | ||
| Carl Ernst | Q107855650 | ||
| Carrie Hanscom | Q114432075 | ||
| Ian Blumenthal | Q114432076 | ||
| Zehra Ordulu | Q114579850 | ||
| Ilaria Kolobova | Q125306138 | ||
| Pamela Sklar | Q17386505 | ||
| Colby Chiang | Q42290458 | ||
| Scott Bell | Q43545877 | ||
| Michael E. Talkowski | Q47502242 | ||
| Santhosh Girirajan | Q47503889 | ||
| Jill A Rosenfeld | Q55712565 | ||
| Ryan L Collins | Q55718373 | ||
| P2093 | author name string | Dimitri J Stavropoulos | |
| Martin Alda | |||
| Steve McCarroll | |||
| Colm O'Dushlaine | |||
| Cristiana Cruceanu | |||
| Jin Szatkiewicz | |||
| Nicolas Menjot de Champfleur | |||
| Melissa T Carter | |||
| Vanessa Ota | |||
| P2860 | cites work | Molecular characterization of 1q44 microdeletion in 11 patients reveals three candidate genes for intellectual disability and seizures | Q59697891 |
| Netrin-G2 and netrin-G2 ligand are both required for normal auditory responsiveness | Q81529466 | ||
| The netrin protein family | Q21183890 | ||
| The netrin-G1 ligand NGL-1 promotes the outgrowth of thalamocortical axons | Q24299100 | ||
| Differential expression of two distinct forms of mRNA encoding members of a dipeptidyl aminopeptidase family | Q24563476 | ||
| Complementary expression and neurite outgrowth activity of netrin-G subfamily members | Q28216202 | ||
| A family-based association study and gene expression analyses of netrin-G1 and -G2 genes in schizophrenia | Q28306895 | ||
| An unbiased expression screen for synaptogenic proteins identifies the LRRTM protein family as synaptic organizers | Q28508414 | ||
| NGL family PSD-95-interacting adhesion molecules regulate excitatory synapse formation | Q28586738 | ||
| Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder | Q28943293 | ||
| Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations | Q29030218 | ||
| Trans-synaptic adhesions between netrin-G ligand-3 (NGL-3) and receptor tyrosine phosphatases LAR, protein-tyrosine phosphatase delta (PTPdelta), and PTPsigma via specific domains regulate excitatory synapse formation | Q33810171 | ||
| A de novo convergence of autism genetics and molecular neuroscience | Q33830989 | ||
| Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research | Q33865401 | ||
| A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders | Q34039999 | ||
| Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders. | Q34288660 | ||
| Clinical diagnosis by whole-genome sequencing of a prenatal sample | Q34315784 | ||
| Dipeptidyl-peptidase-like-proteins confer high sensitivity to the scorpion toxin AmmTX3 to Kv4-mediated A-type K+ channels. | Q34329832 | ||
| Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci | Q34495555 | ||
| Netrin G1 mutations are an uncommon cause of atypical Rett syndrome with or without epilepsy | Q34695209 | ||
| Copy number variation in schizophrenia in Sweden | Q34742638 | ||
| Further delineation of the SATB2 phenotype | Q35150491 | ||
| Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation | Q35669713 | ||
| Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries. | Q35923213 | ||
| Axonal netrin-Gs transneuronally determine lamina-specific subdendritic segments. | Q35970983 | ||
| PopGen: population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships | Q36402170 | ||
| Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilities | Q36451466 | ||
| Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation | Q37156064 | ||
| Protein tyrosine phosphatases PTPδ, PTPσ, and LAR: presynaptic hubs for synapse organization | Q37213119 | ||
| The NGL family of leucine-rich repeat-containing synaptic adhesion molecules | Q37494844 | ||
| Cognitive and behavioral characterization of 16p11.2 deletion syndrome | Q37770943 | ||
| NGL-2 regulates input-specific synapse development in CA1 pyramidal neurons. | Q39239841 | ||
| Describing sequencing results of structural chromosome rearrangements with a suggested next-generation cytogenetic nomenclature | Q41035876 | ||
| Laminets: laminin- and netrin-related genes expressed in distinct neuronal subsets | Q43924921 | ||
| Trans-synaptic adhesion between NGL-3 and LAR regulates the formation of excitatory synapses | Q46104305 | ||
| Profiling brain expression of the spermidine/spermine N1-acetyltransferase 1 (SAT1) gene in suicide | Q46157854 | ||
| Identification and characterization of satellite III subfamilies to the acrocentric chromosomes | Q48367199 | ||
| Netrin-G/NGL complexes encode functional synaptic diversification. | Q48451546 | ||
| Satellite III sequences on 14p and their relevance to Robertsonian translocation formation. | Q51967224 | ||
| Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes. | Q53204200 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | neurodevelopmental disorder | Q3450985 |
| P304 | page(s) | 395-406 | |
| P577 | publication date | 2016-10-19 | |
| P1433 | published in | American Journal of Medical Genetics | Q4744254 |
| P1476 | title | Implication of LRRC4C and DPP6 in neurodevelopmental disorders. | |
| P478 | volume | 173 |
| Q47862323 | A novel Gerstmann-Sträussler-Scheinker disease mutation defines a precursor for amyloidogenic 8 kDa PrP fragments and reveals N-terminal structural changes shared by other GSS alleles. |
| Q58590857 | Convergence of independent DISC1 mutations on impaired neurite growth via decreased UNC5D expression |
| Q52590811 | DPP6 Loss Impacts Hippocampal Synaptic Development and Induces Behavioral Impairments in Recognition, Learning and Memory. |
| Q92891250 | Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes |
| Q60923007 | Identifying Genomic Variations in Monozygotic Twins Discordant for Autism Spectrum Disorder Using Whole-Genome Sequencing |
| Q64908139 | Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability. |
| Q47111463 | Mapping a shared genetic basis for neurodevelopmental disorders. |
| Q92477978 | NGL-1/LRRC4C Deletion Moderately Suppresses Hippocampal Excitatory Synapse Development and Function in an Input-Independent Manner |
| Q39027831 | Netrin G1: its downregulation in the nucleus accumbens of cocaine-conditioned mice and genetic association in human cocaine dependence |
| Q64994782 | Predicting human disease mutations and identifying drug targets from mouse gene knockout phenotyping campaigns. |
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