Paulina Paavola

Comprehensive copy number and gene expression profiling of the 17q23 amplicon in human breast cancer

Outi Monni, Maarit Bärlund, Spyro Mousses et al. · Proceedings of the National Academy of Sciences · 2001 · 253 citations · Full text

The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21–q24

Paulina Paavola, Riitta Salonen, Jean Weissenbach et al. · Nature Genetics · 1995 · 113 citations

Developmental Anomaly, Developmental Biology, Genetic Disorder +4

Familial and Sporadic Inflammatory Bowel Disease: Comparison of Clinical Features and Serological Markers in a Genetically Homogeneous Population

Leena Halme, Ulla Turunen, Tiina Heliö et al. · Scandinavian Journal of Gastroenterology · 2002 · 68 citations

Overall survival after stereotactic radiotherapy or surgical metastasectomy in oligometastatic renal cell carcinoma patients treated at two Swedish centres 2005–2014

Mathias Stenman, G. Sinclair, Paulina Paavola et al. · Radiotherapy and Oncology · 2018 · 66 citations

Urology, Surgical Oncology, Overall Survival +8

Clinical and genetic heterogeneity in Meckel syndrome

Paulina Paavola, Riitta Salonen, Alessandra Baumer et al. · Human Genetics · 1997 · 58 citations · Full text

Mendelian Disorder, Clinical Genetic Disorders, Genetic Disorder +6