J. Papp

Semmelweis University — Hungary

Biochemistry, Genetics and Molecular Biology · Life Sciences

33h-index4.6kcitations259works2.22yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Inflammatory Bowel Disease(39), BRCA gene mutations in cancer(20), Genetic factors in colorectal cancer(20), Plant Physiology and Cultivation Studies(20), Pancreatitis Pathology and Treatment(19)

Publications249 total

Processed Transcript Insertion as a Novel Germline Mutational Mechanism in BRCA1-Associated Hereditary Breast Cancer
Cancers·2025Open Access
Double Pathogenic or Likely Pathogenic Variants in Cancer Predisposition Genes in Hungarian Cancer Patients
International Journal of Molecular Sciences·2025· 2 citedOpen Access
Exploring SDHA variants: navigating predisposition and incidental findings
Endocrine Abstracts·2025
[Pathogenic large duplication in TP53 as a hereditary predisposing factor in breast cancer].
PubMed·2025
[Pathogenic role of CHEK2 variants in Hungarian cancer patients: implications for breast cancer risk and genetic counselling].
PubMed·2025
Gastrointestinalis amyloidosis – retrospektív elemzés egy budapesti centrum adatai alapján
Orvosi Hetilap·2025· 1 citedOpen Access
The impact of glucocorticoid receptor transactivation on context-dependent cell migration dynamics
Scientific Reports·2025· 4 citedOpen Access
Whole genome sequencing completes the molecular genetic testing workflow of patients with Lynch syndrome
npj Genomic Medicine·2025· 4 citedOpen Access
Comprehensive Clinical Genetics, Molecular and Pathological Evaluation Efficiently Assist Diagnostics and Therapy Selection in Breast Cancer Patients with Hereditary Genetic Background
International Journal of Molecular Sciences·2024· 10 citedOpen Access
Spectrum and genotyping strategies of “dark” genetic matter in germline susceptibility genes of tumor syndromes
Critical Reviews in Oncology/Hematology·2024· 1 citedOpen Access
The Impact of Protein Glycosylation on the Identification of Patients with Pediatric Appendicitis
International Journal of Molecular Sciences·2024Open Access
Peripheral immunophenotyping reveals lymphocyte stimulation in healthy women living with hereditary breast and ovarian cancer syndrome
iScience·2024· 1 citedOpen Access
Cost-effectiveness of Genetic Testing of Endocrine Tumor Patients Using a Comprehensive Hereditary Cancer Gene Panel
The Journal of Clinical Endocrinology & Metabolism·2024· 7 citedOpen Access
Adapting to Change: AI’s Potential Impacts on Journalism
Pázmány Law Review·2024· 1 citedOpen Access
Publisher Correction: Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma
Scientific Reports·2023Open Access
Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma
Scientific Reports·2023· 4 citedOpen Access
Challenging interpretation of germline TP53 variants based on the experience of a national comprehensive cancer centre
Scientific Reports·2023· 5 citedOpen Access
PALB2 Variants Extend the Mutational Profile of Hungarian Patients with Breast and Ovarian Cancer
Cancers·2023· 5 citedOpen Access
High diagnostic yield of multigene panel testing in patients with endocrine tumors
Endocrine Abstracts·2023
Genome sequencing-based discovery of a novel deep intronic APC pathogenic variant causing exonization
European Journal of Human Genetics·2023· 9 citedOpen Access
page 1 of 13Next →

Frequent Co-authors

Péter L. Lakatos(35), Mária Papp(13), Edith Oláh(12), I Altorjay(10), Károly Palatka(9), Ágota Kovács(9), Tamás Molnár(9), Zsolt Tulassay(9), Pál Miheller(8), Simon Fischer(8), Tamás Szamosi(7), M. Udvardy(5), Zsolt Tulassay(5), Judit Tumpek(4), Gábor Veres(4), Péter Fuszek(4), Pál Demeter(4), Anikó Bozsik(4), Marietta Eva Kovacs(3), Ildikó Földi(3)