| P50 | author | Merlin Butler | Q57977737 |
| | Syed K Rafi | Q92027361 |
| | Alberto Fernández-Jaén | Q42864302 |
| P2093 | author name string | Owen W Nadeau | |
| | Sara Álvarez | |
| P2860 | cites work | Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority | Q21146621 |
| | I-TASSER server for protein 3D structure prediction | Q21284202 |
| | Towards a proteome-scale map of the human protein–protein interaction network | Q21735930 |
| | A family of Rab27-binding proteins. Melanophilin links Rab27a and myosin Va function in melanosome transport | Q24295585 |
| | Structure of a lipid-bound extended synaptotagmin indicates a role in lipid transfer | Q24298007 |
| | Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly | Q24299324 |
| | A proteome-scale map of the human interactome network | Q24307146 |
| | Elucidation of Rab27 recruitment by its effectors: structure of Rab27a bound to Exophilin4/Slp2-a | Q24336538 |
| | The Protein Data Bank | Q24515306 |
| | Structural basis for chromosome X-linked agammaglobulinemia: a tyrosine kinase disease | Q24564000 |
| | I-TASSER: a unified platform for automated protein structure and function prediction | Q24605680 |
| | Identification of novel families and classification of the C2 domain superfamily elucidate the origin and evolution of membrane targeting activities in eukaryotes | Q24623162 |
| | A quantitative atlas of mitotic phosphorylation | Q24646817 |
| | Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited | Q24647915 |
| | LOMETS: a local meta-threading-server for protein structure prediction | Q24682449 |
| | The amino-acid mutational spectrum of human genetic disease | Q24793270 |
| | Synaptotagmin-1 and synaptotagmin-7 trigger synchronous and asynchronous phases of neurotransmitter release | Q26269844 |
| | Extracellular vesicles round off communication in the nervous system | Q26764878 |
| | Cellular functions of Rab GTPases at a glance | Q26798421 |
| | A mouse model of anxiety molecularly characterized by altered protein networks in the brain proteome. | Q48239883 |
| | STXBP1 promotes Weibel-Palade body exocytosis through its interaction with the Rab27A effector Slp4-a | Q48320838 |
| | Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap. | Q50034912 |
| | A preliminary analysis of association between the down-regulation of microRNA-181b expression and symptomatology improvement in schizophrenia patients before and after antipsychotic treatment. | Q50651086 |
| | An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome | Q55920728 |
| | Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model | Q60045074 |
| | Structural basis of Wiskott-Aldrich syndrome causing mutations in the WH1 domain | Q73350437 |
| | b-series Ganglioside deficiency exhibits no definite changes in the neurogenesis and the sensitivity to Fas-mediated apoptosis but impairs regeneration of the lesioned hypoglossal nerve | Q77079964 |
| | Analysis of the role of Rab27 effector Slp4-a/Granuphilin-a in dense-core vesicle exocytosis | Q82533435 |
| | Characterization and fine localization of two new genes in Xq28 using the genomic sequence/EST database screening approach | Q48063125 |
| | MicroRNA dysregulation in schizophrenia | Q26861195 |
| | Structure of human synaptotagmin 1 C2AB in the absence of Ca2+ reveals a novel domain association | Q27648873 |
| | UCSF Chimera--a visualization system for exploratory research and analysis | Q27860666 |
| | Rab proteins as membrane organizers | Q27860861 |
| | G protein pathways | Q27919625 |
| | MicroRNA-9 controls the expression of Granuphilin/Slp4 and the secretory response of insulin-producing cells | Q28251177 |
| | A protein assembly-disassembly pathway in vitro that may correspond to sequential steps of synaptic vesicle docking, activation, and fusion | Q28255534 |
| | Whole-genome association study of bipolar disorder | Q28271419 |
| | Synaptotagmin I: a major Ca2+ sensor for transmitter release at a central synapse | Q28587672 |
| | Individual common variants exert weak effects on the risk for autism spectrum disorders | Q28943296 |
| | De novo mutations revealed by whole-exome sequencing are strongly associated with autism | Q29547269 |
| | Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations | Q29614573 |
| | STRING v10: protein-protein interaction networks, integrated over the tree of life | Q29615545 |
| | SVD-phy: improved prediction of protein functional associations through singular value decomposition of phylogenetic profiles | Q30002354 |
| | Structural basis of ICF-causing mutations in the methyltransferase domain of DNMT3B. | Q30332535 |
| | Probing the alpha-complementing domain of E. coli beta-galactosidase with use of an insertional pentapeptide mutagenesis strategy based on Mu in vitro DNA transposition. | Q30339082 |
| | Loss of protein structure stability as a major causative factor in monogenic disease. | Q30351402 |
| | Hydrogen bonds involving sulfur atoms in proteins. | Q30362217 |
| | The I-TASSER Suite: protein structure and function prediction. | Q30370293 |
| | Specific Regional and Age-Related Small Noncoding RNA Expression Patterns Within Superior Temporal Gyrus of Typical Human Brains Are Less Distinct in Autism Brains | Q30396876 |
| | Complex salt bridges in proteins: statistical analysis of structure and function | Q30416711 |
| | Using whole-exome sequencing to identify inherited causes of autism | Q30418126 |
| | Association between SNAP-25 gene polymorphisms and cognition in autism: functional consequences and potential therapeutic strategies | Q30419188 |
| | Spectrum of disease-causing mutations in protein secondary structures | Q30500895 |
| | The Rab27a effector exophilin7 promotes fusion of secretory granules that have not been docked to the plasma membrane | Q30534507 |
| | Common genetic variants, acting additively, are a major source of risk for autism | Q30536405 |
| | Colorectal cancer cell-derived microvesicles are enriched in cell cycle-related mRNAs that promote proliferation of endothelial cells | Q30908848 |
| | Evidence for defective Rab GTPase-dependent cargo traffic in immune disorders | Q33408755 |
| | Transcriptional changes in response to X chromosome dosage in the mouse: implications for X inactivation and the molecular basis of Turner Syndrome | Q33528165 |
| | C2A activates a cryptic Ca(2+)-triggered membrane penetration activity within the C2B domain of synaptotagmin I. | Q34010567 |
| | Representing sex in the brain, one module at a time. | Q34033384 |
| | Serum microRNA profiles in children with autism | Q34043327 |
| | Aberrant expression of serum miRNAs in schizophrenia | Q34233578 |
| | The Ras superfamily of small GTPases: the unlocked secrets | Q34400465 |
| | The Mouse Genome Database (MGD): facilitating mouse as a model for human biology and disease | Q34445051 |
| | Evidence for transcriptional factor dysregulation in the dorsal raphe nucleus of patients with major depressive disorder. | Q34453877 |
| | Whole exome sequencing in females with autism implicates novel and candidate genes | Q35016586 |
| | MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro | Q35138690 |
| | Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders | Q35155976 |
| | High-resolution chromosome ideogram representation of currently recognized genes for autism spectrum disorders | Q35381777 |
| | Identification of a human synaptotagmin-1 mutation that perturbs synaptic vesicle cycling | Q35408613 |
| | Exome sequencing can improve diagnosis and alter patient management | Q35641969 |
| | Synaptic dysfunction in neurodevelopmental disorders associated with autism and intellectual disabilities | Q35765423 |
| | Modular genetic control of sexually dimorphic behaviors. | Q35889070 |
| | Hypomethylation of miR-142 promoter and upregulation of microRNAs that target the oxytocin receptor gene in the autism prefrontal cortex | Q35949527 |
| | Rab GTPases implicated in inherited and acquired disorders | Q36090727 |
| | Rab27b is expressed in a wide range of exocytic cells and involved in the delivery of secretory granules near the plasma membrane | Q36095761 |
| | Granuphilin molecularly docks insulin granules to the fusion machinery. | Q36320435 |
| | Replication and meta-analysis of TMEM132D gene variants in panic disorder | Q36589733 |
| | Overshadowed by the amygdala: the bed nucleus of the stria terminalis emerges as key to psychiatric disorders | Q36719172 |
| | A common MECP2 haplotype associates with reduced cortical surface area in humans in two independent populations | Q37340881 |
| | STX1A and Asperger syndrome: a replication study | Q37599630 |
| | The mouse Gene Expression Database (GXD): 2014 update | Q37661857 |
| | GeneAnalytics Pathway Analysis and Genetic Overlap among Autism Spectrum Disorder, Bipolar Disorder and Schizophrenia. | Q37729086 |
| | Presynaptic function in health and disease | Q37877363 |
| | Mechanisms in the bed nucleus of the stria terminalis involved in control of autonomic and neuroendocrine functions: a review | Q38133552 |
| | Solving the molecular diagnostic testing conundrum for Mendelian disorders in the era of next-generation sequencing: single-gene, gene panel, or exome/genome sequencing | Q38252010 |
| | STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy. | Q38729097 |
| | Ultradeep human phosphoproteome reveals a distinct regulatory nature of Tyr and Ser/Thr-based signaling | Q38962630 |
| | The Future of Next-Generation Sequencing in Neurology | Q38987942 |
| | Gene and miRNA expression profiles in autism spectrum disorders | Q39651877 |
| | Functional analysis of Rab27a effector granuphilin in insulin exocytosis | Q40317658 |
| | Novel insights into role of miR-320a-VDAC1 axis in astrocyte-mediated neuronal damage in neuroAIDS. | Q40497318 |
| | Whole-genome sequencing of quartet families with autism spectrum disorder | Q41525456 |
| | The C2 domains of granuphilin are high-affinity sensors for plasma membrane lipids. | Q41901134 |
| | Salt bridges: geometrically specific, designable interactions | Q41989888 |
| | Gene expression profiles of cholinergic nucleus basalis neurons in Alzheimer's disease. | Q42528387 |
| | Rare inherited variation in autism: beginning to see the forest and a few trees | Q43117326 |
| | Modular genetic control of innate behaviors | Q45038807 |
| | The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders | Q45225641 |
| | Heterogeneous dysregulation of microRNAs across the autism spectrum. | Q45942304 |
| | Association of Sex With Recurrence of Autism Spectrum Disorder Among Siblings | Q46432376 |
| | Functional analysis of schizophrenia genes using GeneAnalytics program and integrated databases. | Q47650107 |
| | Protein coding genes as hosts for noncoding RNA expression. | Q47948770 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 13 | |
| P921 | main subject | protein-protein interaction | Q896177 |
| | high-functioning autism | Q1788847 |
| P577 | publication date | 2019-07-09 | |
| P1433 | published in | International Journal of Molecular Sciences | Q3153277 |
| P1476 | title | High Functioning Autism with Missense Mutations in Synaptotagmin-Like Protein 4 (SYTL4) and Transmembrane Protein 187 (TMEM187) Genes: SYTL4- Protein Modeling, Protein-Protein Interaction, Expression Profiling and MicroRNA Studies | |
| P478 | volume | 20 | |