Congenital heart disease: ki dolgozik rajta

Intézményenként egy kártya. Célpontra vagy országra szűkítheted a listát.

• Minden célpont
• ERK 0
• PI3K 0
• SGLT2 4
• AKT 0
• SHP2 0
• AMPK 0
• BRAF 0
• FGFR 0
• MAPK 0
• MMP-9 0
• NOTCH1 0
• NRF2 0
• PPAR 0
• RAS 0
• ABL1 0
• ACE2 0
• APP 0
• BCL-2 0
• CDK4/6 0
• CTNNB1 0
• FAK 0
• FTO 0
• GLP-1 0
• GPC3 0
• HDAC 0
• JAK 0
• JNK 0
• KRAS 0
• mTOR 0
• NF1 0
• NRAS 0
• PTEN 0
• STAT3 0
• STING 0
• TNF 0
• TP53 0
• YAP 0

1182 intézményből 24, a friss publikációk és a nyitott vizsgálatok szerint rendezve. Ez nem minőségi rangsor.

Funded research projects that name this disease in their title, terms or summary and have not ended yet: who is funded, where, how much and until when. Organisations only; the funder's page has the details.

• NIH NICHD · R13

  Clinical Practice Guidelines and Research Priorities for Pediatric Critical Illness Follow-up Care

  Boston Children's Hospital· Boston, Egyesült Államok· 14 111 USD awarded in fiscal year 2026· until 2028. aug.

• NIH NICHD · R01

  Neurodevelopmental Effects of Gestational Gabapentin Exposure

  Georgetown University· Washington, Egyesült Államok· 572 237 USD awarded in fiscal year 2026· until 2031. máj.

• NIH NICHD · R03

  Fine Mapping and Phenotypic Association of Chromosome 18 CNVs in the Gabriela Miller Kids First Pediatrics Research Program

  Pennsylvania State University, the· University Park, Egyesült Államok· 289 075 USD awarded in fiscal year 2026· until 2028. aug.

• NIH NHLBI · R21

  AI-facilitated Echocardiography for Early Detection of Acyanotic Congenital Heart Disease in Infants

  Health Research Foundation· Buea, Kamerun· 74 995 USD awarded in fiscal year 2026· until 2028. aug.

• NIH NICHD · R21

  A trisomic porcine model for studying Down syndrome in the gyrencephalic brain

  Boston University Medical Campus· Boston, Egyesült Államok· 449 625 USD awarded in fiscal year 2026· until 2028. aug.

• European Commission (Horizon Europe) · HORIZON-ERC

  Switching cardiomyocyte activity to uncover biology and treat disease. (CARDIOSWITCH)

  Centro Nacional de Investigaciones Cardiovasculares Carlos Iii (F.s.p.)· Madrid, Spanyolország· EU contribution 2 428 125 EUR· until 2031. okt.

  The disease is named only in the funder's project summary, not in the title.

• European Commission (Horizon Europe) · HORIZON-IA

  OPTIMISING THE MANUFACTURING PLATFORM FOR INDIVIDUALIZED IPS CELL BASED HEART REPAIR (iNDUCARE)

  Medizinische Hochschule Hannover· Hannover, Németország· EU contribution 7 985 334 EUR· until 2030. aug.· 7 countries

  The disease is named only in the funder's project summary, not in the title.

• European Commission (Horizon Europe) · HORIZON-ERC-POC

  Congenital Heart Anomaly Representation and Machine-learning for Screening (CHARMS)

  Imperial College of Science Technology and Medicine· London, Egyesült Királyság· EU contribution 150 000 EUR· until 2027. jún.

  The disease is named only in the funder's project summary, not in the title.

• European Commission (Horizon Europe) · HORIZON-EIC

  Polymer-based Stealth Coating of Hemocompatible and Absorbable Stents (StealthStent)

  Biomodics Aps· Kgs Lyngby, Dánia· EU contribution 2 495 679 EUR· until 2028. márc.· 2 countries

  The disease is named only in the funder's project summary, not in the title.

• European Commission (Horizon Europe) · HORIZON-ERC

  Beyond the chromosome: unravelling the interplay between inter-chromosomal genome architecture and mRNA biogenesis (TRANS-3)

  Universita Degli Studi di Torino· Torino, Olaszország· EU contribution 1 769 998 EUR· until 2028. aug.

10 of 378 running projects, newest first. Listed amounts together: 220,8 M USD + 19,8 M EUR.

Sources: NIH RePORTER (U.S. National Institutes of Health, public domain) and CORDIS (European Commission, CC BY 4.0). Changes: filtered by disease, organisations matched to ROR.

Leállított, visszavont és felfüggesztett vizsgálatok, a szponzor által a regiszterben megadott okkal, szó szerint idézve.

• Leállították

  Strong Hearts: A Remote, App-Enabled, Exercise Program for Patients With Congenital Heart Disease (Strong Hearts App)

  NCT05853705· Duke University· Frissítve: 2026. aug. 5.

  “Low participation rate”A regiszter szövege, változtatás nélkül. Forrás

• Visszavonták

  Artificial Intelligence-enabled ECG Detection of Congenital Heart Disease in Children: a Novel Diagnostic Tool

  NCT06383546· Xinhua Hospital, Shanghai Jiao Tong University School of Medicine· Frissítve: 2026. júl. 29.

  “Repeated application of the same project”A regiszter szövege, változtatás nélkül. Forrás

• Visszavonták

  Empiric Pulsed Field Pulmonary Vein Isolation During Atrial Tachycardia Ablation in Adults With Congenital Heart Disease

  NCT06969378· Boston Children's Hospital· Frissítve: 2026. júl. 14.

  “Never started”A regiszter szövege, változtatás nélkül. Forrás

• Leállították

  Characterizing the Effect of Dopamine on Markers of Lymph Re-circulation in Fontan-associated Protein-losing Enteropathy

  NCT03322345· University of Michigan· Frissítve: 2026. júl. 14.

  “Inadequate patient enrollment”A regiszter szövege, változtatás nélkül. Forrás

• Felfüggesztve

  Propranolol Treatment for Postoperative Chylothorax

  NCT06833320· June Wu· Frissítve: 2026. máj. 15.

  “Administrative changes”A regiszter szövege, változtatás nélkül. Forrás

• Visszavonták

  A Study of Pregnancy Outcomes in Congenital Heart Disease

  NCT06678256· Mayo Clinic· Frissítve: 2026. márc. 19.

  “Lack of funding”A regiszter szövege, változtatás nélkül. Forrás

• Visszavonták

  Impedance During Cardiac Catheterization to Build a Non-Invasive Cardiac Output Algorithm

  NCT06171698· Johns Hopkins University· Frissítve: 2025. júl. 14.

  “Closed at site. Investigator no longer at location.”A regiszter szövege, változtatás nélkül. Forrás

• Leállították

  Evaluation of an Investigational Wearable Vital Signs Monitoring Device in Healthy Infants

  NCT05910320· Johns Hopkins University· Frissítve: 2025. júl. 10.

  “Closed at site. Investigator no longer at site.”A regiszter szövege, változtatás nélkül. Forrás

• Visszavonták

  Partial Heart Transplantation

  NCT06055556· Duke University· Frissítve: 2025. júl. 1.

  “Study no longer needed.”A regiszter szövege, változtatás nélkül. Forrás

• Leállították

  A Study Evaluating the Efficacy and Safety of IV L-Citrulline for the Prevention of Clinical Sequelae of Acute Lung Injury Induced by Cardiopulmonary Bypass in Pediatric Patients Undergoing Surgery for Congenital Heart Defects

  NCT05253209· Asklepion Pharmaceuticals, LLC· Frissítve: 2024. szept. 19.

  “Interim Analysis triggered futility”A regiszter szövege, változtatás nélkül. Forrás

Vizsgálatok, amelyek regiszteradata szerint az egyéni résztvevői adatokat (IPD) megosztják.

• Butyric Acid Supplementation for Gut Improvement After Cardiac Surgery in Kids

  NCT06882772· University of Nebraska· Forrás

• A Pragmatic Clinical Trial of the WE BEAT Well-Being Education Program in Adolescent Congenital Heart Disease: WE BEAT CHD Study

  NCT07525843· Carelon Research· Forrás

• Fontan Associated Liver Disease and the Evaluation of Biomarkers for Disease Severity Assessment

  NCT05213598· National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)· Forrás

• Comparison of Erector Spinae Plane Block and Modified Pectoral Fascial Plane Block for Postoperative Analgesia in Pediatric Cardiac Surgery

  NCT07740915· Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital· Forrás

• Skin Pigment/Pulse Oximeter in Congenital Heart Disease (CHD)

  NCT06575270· Icahn School of Medicine at Mount Sinai· Forrás

• Prenatally-initiated Psychological Intervention for Mothers of Infants With Congenital Heart Disease (CHD)

  NCT07582861· Carelon Research· Forrás

• BOND: Direct Breastfeeding to Enhance Maternal and Infant Health in Congenital Heart Disease

  NCT07582848· Carelon Research· Forrás

• Bilateral Ultrasound Guided Superficial Parasternal Intercostal Plane Block Versus Erector Spinae Plane Block

  NCT06958120· Cairo University· Forrás

• Development of Methods for Effective Treatment and Improvement of Common Somatic Diseases in Children

  NCT06267859· Tashkent State Medical University (Tashkent Pediatric Medical Institute), Uzbekistan· Forrás

• Effects of Exercise in Patients With Repaired Coarctation of the Aorta

  NCT07771023· University Medical Centre Ljubljana· Forrás

Publikációk erről a betegségről egy MeSH-módszerkifejezés szerint, például szekvenálási vagy képalkotó módszerre.

• Single-Cell Analysis 9
• Organoids 6
• Mendelian Randomization Analysis 3
• CRISPR-Cas Systems 5
• Gene Expression Profiling 12
• Whole Genome Sequencing 11
• Exome Sequencing 58
• Proteomics 16
• Metabolomics 8
• Mass Spectrometry 4
• Immunohistochemistry 3
• Positron-Emission Tomography 1
• Magnetic Resonance Imaging 135
• Machine Learning 35
• Deep Learning 26
• Cohort Studies 112
• Genome-Wide Association Study 12

• Discovery of novel alleles in Kartagener's syndrome.

  Mamm Genome, 2026. okt.

• Variants in CEP135 Cause Congenital Microcephaly and Primary Ciliary Dyskinesia.

  Pediatr Pulmonol, 2026. okt.

• Clinical and Molecular Delineation of KAT6B-Related Disorders: Novel Variants and Refined Genotype-Phenotype Correlations.

  Hum Mutat, 2026. szept.

• Genetic Spectrum of Cholestasis in Tunisia and Diagnostic Yield of Next-Generation Sequencing: Case Series of 70 Patients.

  Clin Genet, 2026. szept.

• Pathology of Genetic Variants in Spontaneous Coronary Artery Dissection.

  Circulation, 2026. szept.

• A novel de novo multi-exon deletion of SYT1 in a child with Baker-Gordon syndrome.

  BMC Pediatr, 2026. aug.

• Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

  Sci Rep, 2026. aug.

• Genetics in Heterotaxy: A Case Series and Literature Review on DNAH9, PKD1L1, MMP21, and GDF1.

  Clin Genet, 2026. aug.

• Identification and characterisation of a novel homozygous KDM5A variant associated with severe axial hypotonia, seizures, and cardiac anomalies.

  J Hum Genet, 2026. aug.

• Clinical and Genetic Profile of One Molecularly Confirmed and One Clinically Suspected Case of LZTR1 -Related Noonan Syndrome.

  Clin Genet, 2026. aug.

Megmutatjuk, a betegség mely célpontjait említi az absztrakt, és onnan a rajtuk dolgozókhoz jutsz.