| scholarly article | Q13442814 |
| P50 | author | Andreas Friebe | Q87632544 |
| Dieter Groneberg | Q95975128 | ||
| P2093 | author name string | Eugen Zizer | |
| Gudrun Rappold | |||
| Beate Niesler | |||
| Henning Fröhlich | |||
| Amelie Reigl | |||
| Manuel Stuhlinger | |||
| Marie Luise Kollmeyer | |||
| Valerie Catherine Linz | |||
| P2860 | cites work | Evaluation, Diagnosis, and Treatment of Gastrointestinal Disorders in Individuals With ASDs: A Consensus Report | Q22241500 |
| Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy | Q24313460 | ||
| Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology | Q26770773 | ||
| FoxP1 orchestration of ASD-relevant signaling pathways in the striatum | Q27322723 | ||
| Serotonin transporter variant drives preventable gastrointestinal abnormalities in development and function | Q27329816 | ||
| The bowel and beyond: the enteric nervous system in neurological disorders | Q28069344 | ||
| Mutant WD-repeat protein in triple-A syndrome | Q28142964 | ||
| Gastrointestinal symptoms in autism spectrum disorder: a meta-analysis | Q28239007 | ||
| Foxp2 and Foxp1 cooperatively regulate lung and esophagus development | Q28508512 | ||
| Foxp1 regulates cardiac outflow tract, endocardial cushion morphogenesis and myocyte proliferation and maturation | Q28513688 | ||
| Nexilin: a novel actin filament-binding protein localized at cell-matrix adherens junction | Q28571541 | ||
| A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus | Q28943522 | ||
| Disruption of the glucocorticoid receptor gene in the nervous system results in reduced anxiety | Q29615160 | ||
| Gpr177 regulates pulmonary vasculature development | Q30410961 | ||
| Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour | Q30412243 | ||
| Autism gene variant causes hyperserotonemia, serotonin receptor hypersensitivity, social impairment and repetitive behavior | Q30462749 | ||
| Foxp1 is an essential transcriptional regulator for the generation of quiescent naive T cells during thymocyte development. | Q33608726 | ||
| Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits | Q34024006 | ||
| Next-generation sequencing of endoscopic biopsies identifies ARID1A as a tumor-suppressor gene in Barrett's esophagus | Q34547790 | ||
| Foxp1 regulates cortical radial migration and neuronal morphogenesis in developing cerebral cortex | Q35641253 | ||
| Gastrointestinal dysfunction in autism: parental report, clinical evaluation, and associated factors | Q35910826 | ||
| A newly identified susceptibility locus near FOXP1 modifies the association of gastroesophageal reflux with Barrett's esophagus | Q36753025 | ||
| Mutations in GMPPA cause a glycosylation disorder characterized by intellectual disability and autonomic dysfunction | Q37217021 | ||
| Low expression of RBMS3 and SFRP1 are associated with poor prognosis in patients with gastric cancer | Q37447944 | ||
| Pitt-Hopkins Syndrome: intellectual disability due to loss of TCF4-regulated gene transcription. | Q38103810 | ||
| FOXP1-related intellectual disability syndrome: a recognisable entity | Q38666337 | ||
| Motility patterns in mouse colon: gastrointestinal dysfunction induced by anticancer chemotherapy | Q39021857 | ||
| Conservation of trans-acting circuitry during mammalian regulatory evolution | Q39843784 | ||
| Gastrointestinal symptoms in autism spectrum disorder: A review of the literature on ascertainment and prevalence | Q40063696 | ||
| Loss of mammalian Sprouty2 leads to enteric neuronal hyperplasia and esophageal achalasia | Q40413223 | ||
| Dominant role of interstitial cells of Cajal in nitrergic relaxation of murine lower oesophageal sphincter | Q41513725 | ||
| Disrupted nitric oxide signaling due to GUCY1A3 mutations increases risk for moyamoya disease, achalasia and hypertension. | Q41637594 | ||
| Lower esophageal sphincter is achalasic in nNOS(-/-) and hypotensive in W/W(v) mutant mice | Q42506766 | ||
| Loss of Lsc/p115 protein leads to neuronal hypoplasia in the esophagus and an achalasia-like phenotype in mice | Q42989143 | ||
| Prospective investigation of FOXP1 syndrome. | Q43806509 | ||
| Importance of preoperative and postoperative pH monitoring in patients with esophageal achalasia. | Q46014190 | ||
| The prevalence of gastrointestinal problems in children across the United States with autism spectrum disorders from families with multiple affected members. | Q46020123 | ||
| Prevalence of increased esophageal muscle thickness in patients with esophageal symptoms | Q46124393 | ||
| Foxp1 regulation of neonatal vocalizations via cortical development. | Q47402230 | ||
| Foxp1 in Forebrain Pyramidal Neurons Controls Gene Expression Required for Spatial Learning and Synaptic Plasticity. | Q47619822 | ||
| Interstitial cells of Cajal mediate enteric inhibitory neurotransmission in the lower esophageal and pyloric sphincters | Q47787241 | ||
| Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia. | Q48292937 | ||
| Megaoesophagus in Rassf1a-null mice. | Q51742752 | ||
| FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability? | Q53081210 | ||
| Downregulation of RBMS3 is associated with poor prognosis in esophageal squamous cell carcinoma. | Q54567714 | ||
| Nexilin/NEXN controls actin polymerization in smooth muscle and is regulated by myocardin family coactivators and YAP | Q58695777 | ||
| Intestinal dysmotility in a zebrafish () mutant model of autism | Q61805365 | ||
| Truncating Mutation in the Nitric Oxide Synthase 1 Gene Is Associated With Infantile Achalasia | Q62779649 | ||
| Barrett's esophagus in a patient with achalasia | Q70101601 | ||
| Barrett's esophagus after cardiomyotomy for esophageal achalasia | Q72764223 | ||
| Achalasia | Q87121698 | ||
| Murine genetic deficiency of neuronal nitric oxide synthase (nNOS(-/-) ) and interstitial cells of Cajal (W/W(v) ): Implications for achalasia? | Q87654028 | ||
| Cell-specific effects of nitric oxide on the efficiency and frequency of long distance contractions in murine colon | Q92853189 | ||
| P433 | issue | 44 | |
| P921 | main subject | achalasia | Q661015 |
| P304 | page(s) | 22237-22245 | |
| P577 | publication date | 2019-10-14 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Gastrointestinal dysfunction in autism displayed by altered motility and achalasia in Foxp1 +/- mice | |
| P478 | volume | 116 |
| Q95933684 | Emerging evidence for gene mutations driving both brain and gut dysfunction in autism spectrum disorder | cites work | P2860 |
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