• A case report of fludarabine associated ectopic atrial bradycardia and literature review of fludarabine induced bradycardia
• A comprehensive study evaluating germline FANCG variants in predisposition to breast and ovarian cancer
• A minimal Fanconi Anemia complex in early diverging fungi
• A naturally occurring canine model of syndromic congenital microphthalmia
• A Novel Autosomal Recessive Candidate Gene Responsible for RASopathy-Like Phenotype and Bone Marrow Failure: <em>RASA3</em>
• A Nutrigenomic View on the Premature-Aging Disease Fanconi Anemia
• A Rare Case Report of Fanconi Anemia-Associated Nuclease 1 Mutation Causing Nephrotic Syndrome
• A Review of the Repair of DNA Double Strand Breaks in the Development of Oral Cancer
• Advanced Analysis and Validation of a microRNA Signature for Fanconi Anemia
• ALDH2 mutations and defense against genotoxic aldehydes in cancer and inherited bone marrow failure syndromes
• Aplastic anemia
• Associated Congenital Abnormalities and Physical Phenotype in Patients with Diamond-Blackfan Anemia May Be Overlooked
• Bayesian meta-analysis of penetrance for cancer risk
• Benign tumors and non-melanoma skin cancers in patients with Fanconi anemia
• Biallelic FANCA variants detected in sisters with isolated premature ovarian insufficiency
• Cancer Precursor Syndromes and Their Detection in the Head and Neck
• CCAR1 promotes DNA repair via alternative splicing
• Cisplatin-induced bone marrow failure in an adult patient with Fanconi anemia
• Citrinin Provoke DNA Damage and Cell-Cycle Arrest Related to Chk2 and FANCD2 Checkpoint Proteins in Hepatocellular and Adenocarcinoma Cell Lines
• Clinical and biological perspectives on non-canonical esophageal squamous cell carcinoma in rare subtypes
• Clinical utility of relative telomere length analysis in pediatric bone marrow failure
• Clinical Validation of the Somatic FANCD2 Mutation (c.2022-5C&gt;T) as a Novel Molecular Biomarker for Early Disease Progression in Chronic Myeloid Leukemia: A Case-Control Study
• Cost-Effectiveness of Unselected Multigene Germline and Somatic Genetic Testing for Epithelial Ovarian Cancer
• Crosstalk between DNA Damage Repair and Metabolic Regulation in Hematopoietic Stem Cells
• Crucial role of the NSE1 RING domain in Smc5/6 stability and FANCM-independent fork progression
• Cutibacterium acnes invades prostate epithelial cells to induce BRCAness as a possible pathogen of prostate cancer
• Deciphering the role of post-translational modifications in fanconi anemia proteins and their influence on tumorigenesis
• Deficiency of Adenosine Deaminase 2
• Diagnosing Fanconi Anemia: A Rare Case Report From Rural India
• Diagnosis, treatment, and surveillance of Diamond-Blackfan anaemia syndrome: international consensus statement
• Diseases with oral malignant potential: Need for change to inform research, policy, and practice
• Donor-type bone marrow aplasia following hematopoietic stem cell transplantation in a child with a novel <em>SAMD9L</em> variant
• Dual role of proliferating cell nuclear antigen monoubiquitination in facilitating Fanconi anemia-mediated interstrand crosslink repair
• Dynamic Tracking of Native Polyclonal Hematopoiesis in Adult Mice
• Expression of Concern: The RSF1 Histone-Remodelling Factor Facilitates DNA Double-Strand Break Repair by Recruiting Centromeric and Fanconi Anaemia Proteins
• Failure to Thrive With Severe Hypokalemia Yields Cystinosis Diagnosis in a 19-Month-Old Female Child: A Case Report
• FANCD2 counteracts O⁶-methylguanine-induced mismatch repair-dependent apoptosis
• FANCM promotes PARP inhibitor resistance by minimizing ssDNA gap formation and counteracting resection inhibition
• Fanconi Anaemia associated with cafe au lait spots: A rare case report
• Fanconi Anemia Complicated by Cervical Precancer, Vulvar, and Oral Squamous Cell Cancer
• Fanconi Anemia in a 31-Year-Old Patient with Multiple Malignant Tumor Foci, Including Appendiceal Cancer, and Multiple Coexisting Pathologies
• Fanconi Anemia, AML, and MDS
• G-quadruplexes are a source of vulnerability in <em>BRCA2</em> deficient granule cell progenitors and medulloblastoma
• Gemcitabine as chemotherapy of head and neck cancer in Fanconi anemia patients
• Genomic alterations in two patients with esophageal carcinosarcoma identified by whole genome sequencing: a case report
• Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study
• Hematopoiesis post anti-CD117 monoclonal antibody treatment in wild-type and Fanconi anemia settings
• Histological and molecular difference in albumen quality between post-adolescent hens and aged hens
• Histone-methyltransferase KMT2D deficiency impairs the Fanconi anemia/BRCA pathway upon glycolytic inhibition in squamous cell carcinoma
• Homozygous Variant of FANCM of the Fanconi Anemia Pathway Causes Premature Ovarian Insufficiency: Investigation of the Pathogenic Mechanism
• HPV induced R-loop formation represses innate immune gene expression while activating DNA damage repair pathways
• Identification of the ferroptosis-related prognostic gene signature in mesothelioma
• Immunohistochemical findings and clinicopathological features of breast cancers with pathogenic germline mutations in Non-BRCA genes
• In Fanconi anemia, impaired accumulation of bone marrow neutrophils during emergency granulopoiesis induces hematopoietic stem cell stress
• In Utero Hematopoietic Stem Cell Transplantation for Fanconi Anemia
• Infrequent fractures and resilient bone mineral density: bone health in patients with Fanconi anemia
• Integrated proteogenomic analysis for inherited bone marrow failure syndrome
• Karyomegalic Interstitial Nephritis in the Allograft Kidney - A Case Report
• Karyomegalic interstitial nephritis, a fascinating histopathologic entity for pathologists: Be watchful of the FAN1 gene mutations
• Lentivirus-mediated gene therapy corrects ribosomal biogenesis and shows promise for Diamond Blackfan anemia
• Long-term combination therapy with metformin and oxymetholone in a Fanconi anemia mouse model
• Longitudinal clinical manifestations of Fanconi anemia: A systematized review
• Loss of CD5-positive T-cells following anti-thymocyte globulin treatment
• MASCC/ISOO Clinical Practice Statement: The risk of secondary oral cancer following hematopoietic cell transplantation
• Mechanisms of the Effect of Maternal Age-Related Oocyte Aging on Fertility: Transcriptomic Sequencing Analysis of a Zebrafish Model
• Medulloblastoma in children with Fanconi anemia: Association with FA-D1/FA-N, SHH type and poor survival independent of treatment strategies
• Men with metastatic prostate cancer carrying a pathogenic germline variant in breast cancer genes: disclosure of genetic test results to relatives
• Mutation characteristics of cancer susceptibility genes in Chinese ovarian cancer patients
• NEIL3: A unique DNA glycosylase involved in interstrand DNA crosslink repair
• Optical Genome Mapping as a New Tool to Overcome Conventional Cytogenetics Limitations in Patients with Bone Marrow Failure
• Oral health-related quality of life in Fanconi anemia: a cross-sectional study
• Outcome of Hematopoietic Stem Cell Transplantation in 813 Pediatric Patients with Fanconi Anemia
• PALB2-mutated human mammary cells display a broad spectrum of morphological and functional abnormalities induced by increased TGFβ signaling
• PCAF promotes R-loop resolution via histone acetylation
• Pediatric acute promyelocytic leukemia and Fanconi anemia: Case report and literature review
• Phenotypic Variability and Cutaneous Features in 2 Siblings with Fanconi Anaemia and FANCA Mutation
• Predictive modeling of gene mutations for the survival outcomes of epithelial ovarian cancer patients
• Recruitment and Retention of Hematopoietic Cell Transplantation and Cellular Therapy Physicians: A Report from the ASTCT Talent Acquisition Task Force
• Reduced anti-Müllerian hormone levels in males with inherited bone marrow failure syndromes
• Removal of TREX1 activity enhances CRISPR-Cas9-mediated homologous recombination
• Research progress on the fanconi anemia signaling pathway in non-obstructive azoospermia
• Reversion from basal histone H4 hypoacetylation at the replication fork increases DNA damage in FANCA deficient cells
• Role of the mesenchymal stromal cells in bone marrow failure of Fanconi Anemia patients
• Spatial organization and functions of Chk1 activation by TopBP1 biomolecular condensates
• Spectrum and characteristics of germline PALB2 pathogenic variants in 1556 early-onset breast cancer patients in China
• Splicing regulation of DNA repair via CCAR1
• STIL facilitates the development and malignant progression of triple-negative breast cancer through activation of Fanconi anemia pathway via interacting with KLF16
• The Compromised Fanconi Anemia Pathway in Prelamin A-Expressing Cells Contributes to Replication Stress-Induced Genomic Instability
• The critical role of the iron-sulfur cluster and CTC components in DOG-1/BRIP1 function in Caenorhabditis elegans
• The DNA Damage Response (DDR) landscape of endometrial cancer defines discrete disease subtypes and reveals therapeutic opportunities
• The Fanconi anemia core complex promotes CtIP-dependent end resection to drive homologous recombination at DNA double-strand breaks
• The guidelines for clinical practice for carriers of germline mutations in hereditary breast, ovarian, prostate, and pancreatic cancer predisposition genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 (4.2024)
• The role of SLFN11 in DNA replication stress response and its implications for the Fanconi anemia pathway
• The splicing factor CCAR1 regulates the Fanconi anemia/BRCA pathway
• The state of the art in the treatment of severe aplastic anemia: immunotherapy and hematopoietic cell transplantation in children and adults
• Transformation of an abnormal karyotype to acute erythroid leukemia in a pediatric patient with Fanconi anemia: A case report
• Two cases of cytopenia associated with multiple malformations
• Two siblings with Fanconi anemia (FANCQ, ERCC4/XPF) presenting with tumor-mimicking lesions in the brain and acute neurological deterioration
• Update on the Use of Thrombopoietin-Receptor Agonists in Pediatrics
• Updates on germline predisposition in pediatric hematologic malignancies: What is the role of flow cytometry?