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Review Cycle Records

Hereditary Cancer in Clinical Practice

Springer SCIE OA
2026 Emerging Zone 32025 CAS Zone 42025 JCR Q3
135.5Average days
116Median days
19Fastest days
303Longest days
282025 publications

Paper Review Records

All Paper Review Records

10 valid samples · Newest publication first
Review days = acceptance date − received date. PDF, DOI, and publisher-page sources are retained.

19 days

Association analysis of germline variants in GEN1 with a susceptibility to prostate cancer in Polish men

AuthorsKatarzyna Gliniewicz; Klaudia Stempa; Dominika Wokołorczyk; Wojciech Kluźniak; Milena Kiljańczyk; Helena Rudnicka; Tomasz Huzarski; Jacek Gronwald; Jan Uciński; Tadeusz Dębniak; Marta Grabarczyk; Anna Jakubowska; Marek Szwiec; Marcin Lener; Jan Lubiński; Steven A. Narod; Mohammad R. Akbari; Cezary Cybulski

Affiliations1. International Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University in Szczecin, Szczecin, Poland; 2. Department of Clinical Genetics and Pathology, University of Zielona Góra, Zielona Góra, Poland; 3. Independent Laboratory of Molecular Biology and Genetic Diagnostics, Pomeranian Medical University, Szczecin, Poland; 4. Clinics of Oncology, University Hospital in Zielona Góra, Zielona Góra, Poland; 5. Women’s College Hospital, Women’s College Research Institute, University of Toronto, Toronto, Canada; 6. Dalla Lana School of Public Health, University of Toronto, Toronto, Canada

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303 days

Are current Polish guidelines for prophylactic mastectomy sufficient?

AuthorsAdam Stachowski; Cezary Cybulski; Jacek Gronwald; Tomasz Huzarski; Tadeusz Dębniak; Tomasz Byrski; Steven Narod; Rodney Scott; Jan Lubiński

Affiliations1. Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland; 2. Oncology and Chemotherapy Clinic, University Clinical Hospital no. 2 of the Pomeranian Medical University in Szczecin, Szczecin, Poland; 3. Women’s College Research Institute, Women’s College Hospital, University of Toronto, Toronto, Canada; 4. Centre for Cancer Detection and Therapy, Hunter Medical Research Institute, School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, University of Newcastle, Newcastle, Australia; 5. Division of Molecular Medicine, Pathology North, John Hunter Hospital, New Lambton, Australia

Source PDF DOI Publisher page
108 days

Renal cell carcinoma risk among individuals heterozygous for fumarate hydratase variants: further insights into genotype-phenotype correlations

AuthorsTrevor L. Hoffman; Sony Wirio; Vivek Sethumadhavan

Affiliations1. Department of Genetics, Southern California Kaiser Permanente Medical Group, Pasadena, USA; 2. Bernard J. Tyson School of Medicine, Kaiser Permanente, Pasadena, USA; 3. Department of Pathology, Southern California Kaiser Permanente Medical Group, Pasadena, USA

Source PDF DOI Publisher page
124 days

Breast cancer specialists’ experiences and attitudes towards mainstream genetic testing for patients with breast cancer

AuthorsKirsten Allan; Linda Cicciarelli; Catherine Beard; Geoffrey J. Lindeman; G. Bruce Mann; Paul A. James; Laura E. Forrest

Affiliations1. Department of Paediatrics, The University of Melbourne, Parkville, Australia; 2. Parkville Familial Cancer Centre, Peter MacCallum Cancer Centre, Melbourne, Australia; 3. Department of Medicine, The University of Melbourne, Parkville, Australia; 4. The Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia; 5. Department of Surgery, The University of Melbourne, Parkville, Australia; 6. Sir Peter MacCallum, Department of Oncology, The University of Melbourne, Parkville, Australia

Source PDF DOI Publisher page
186 days

Monitoring and treatment patterns of von Hippel-Lindau disease-associated central nervous system hemangioblastomas

AuthorsEric Jonasch; Yan Song; Jonathan Freimark; Manasi Mohan; James Signorovitch; Murali Sundaram

Affiliations1. The University of Texas MD Anderson Cancer Center, Houston, USA; 2. Analysis Group, Inc., Boston, USA; 3. Merck & Co., Inc., Rahway, USA

Source PDF DOI Publisher page
106 days

Impact of germline MMR gene variants on immune checkpoint inhibitors response in patients with MSI-H/dMMR digestive cancers: a retrospective cohort analysis

AuthorsAntoine Dardenne; Camille Loisel; Anna Pellat; Alexandre Perrier; Julie Metras; Thomas Samaille; Yann Parc; Julie Leclerc; Romain Cohen; Thierry André

Affiliations1. Department of Medical Oncology, Saint-Antoine Hospital, AP-HP , Sorbonne University, Paris, France; 2. Department of Genetics, AP-HP, Pitié-Salpêtrière University Hospital, Sorbonne University, Paris, France; 3. Department of Digestive Surgery, AP-HP, Saint-Antoine Hospital, Sorbonne University, Paris, France; 4. Digestive Oncology Department, Gastroenterology, Digestive Endoscopy, Cochin Hospital, AP-HP Centre, Paris, France; 5. Faculty of Médecine, Paris Cité University, Paris, France; 6. Paris Cité University and Sorbonne Paris Nord University, INSERM, INRAe, Center for Research in Epidemiology and Statistics (CRESS), Hôtel Dieu Hospital, Paris, France; 7. Lille University, CNRS, INSERM, CHU Lille, UMR9020-U1277 - CANTHER - Cancer Heterogeneity Plasticity and Resistance to Therapies, Lille, France; 8. Molecular Oncogenetics Unit, Department of Biochemistry and Molecular Biology, Lille University Hospital, Lille, France; 9. Unité Mixte de Recherche Scientifique 938 and SIRIC CURAMUS, Centre de Recherche Saint-Antoine Hospital, Equipe Instabilité des Microsatellites et Cancer, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Inserm, Paris, France

Source PDF DOI Publisher page
60 days

Importance of genetic testing in childhood cancer survivors for hereditary cancer predisposition syndromes

AuthorsAnja Urbas; Polona Ušaj; Boštjan Šeruga; Mateja Krajc; Simona Hotujec; Vida Stegel; Lorna Zadravec Zaletel

Affiliations1. Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia; 2. Division of Medical Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia; 3. Department of Clinical Cancer Genetics, Institute of Oncology Ljubljana, Ljubljana, Slovenia; 4. Department of Molecular Diagnostics, Institute of Oncology Ljubljana, Ljubljana, Slovenia; 5. Biotechnical Faculty, University of Ljubljana, Ljubljana, Slovenia; 6. Division of Radiotherapy, Institute of Oncology Ljubljana, Ljubljana, Slovenia

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82 days

Challenging interpretation of low-level PTCH1 mosaicism in patients with clinically diagnosed Gorlin syndrome: a case series and review of the literature

AuthorsTanya M. Dwarte; Rozanna Alli; Shweta Srinivasa; Fallon Noon; Sumudu Perera Kimmantudawage; Lisa Gordon; Victoria Beshay; Anthony M. Joshua; Raquel Ruiz Araujo; Chris Jalilian; David M. Thomas; Miriam J. Smith; Ingrid Winship; Mandy L. Ballinger; Minmin Li; Katherine M. Tucker; Eliza K. Courtney

Affiliations1. Hereditary Cancer Centre, Prince of Wales Hospital, Randwick, Australia; 2. Genetic Health Queensland, Brisbane, Australia; 3. Family Cancer Service, Westmead Hospital, Westmead, Australia; 4. Genomic Medicine, Royal Melbourne Hospital, Parkville, Australia; 5. Molecular Pathology, Peter MacCallum Cancer Centre, Melbourne, Australia; 6. The Kinghorn Cancer Centre, St Vincent’s Hospital, Garvan Institute of Medical Research, Darlinghurst, Australia; 7. School of Clinical Medicine, UNSW Medicine and Health, UNSW Sydney, Sydney, Australia; 8. Department of Dermatology, Westmead Hospital, Westmead, Australia; 9. Sydney Medical School, Faculty of Medicine and Health, The University of Sydney, Sydney, Australia; 10. Skin Health Institute, Melbourne, Australia; 11. Monash Health, Melbourne, Australia; 12. Centre for Molecular Oncology, UNSW Sydney, Sydney, Australia; 13. Omico, Sydney, Australia; 14. Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK; 15. Manchester Centre for Genomic Medicine, St Mary’s Hospital, Central Manchester University Hospitals, NSH Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK; 16. Department of Medicine, University of Melbourne, Parkville, Australia; 17. Children’s Cancer Institute, Lowy Cancer Centre, UNSW Sydney, Sydney, Australia; 18. Kids Cancer Centre, Sydney Children’s Hospital, Randwick, Australia

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214 days

Genomic profiling in Bulgarian women with ovarian cancer: a dual-sample NGS approach

AuthorsZornitsa Kamburova; Savelina Popovska; Chavdar Tsvetkov

Affiliations1. Department of Medical Genetics, Faculty of Pharmacy, Medical University, Pleven, Bulgaria; 2. Centre of Competence in Personalized Medicine, 3D and Telemedicine, Robotic Assisted and Minimally Invasive Surgery – “Leonardo da Vinci”, Pleven, Bulgaria; 3. Department of General and Clinical Pathology, Faculty of Medicine, Medical University, Pleven, Bulgaria; 4. Department of Midwifery Care, Faculty of Health Care, Medical University, Pleven, Bulgaria

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153 days

A retrospective analysis of risk-reducing salpingo-oophorectomy performed in women diagnosed with hereditary breast and ovarian cancer at our institution

AuthorsYusaku Shimizu; Miho Kitai; Masashi Akada; Michihide Maeda; Eri Yamabe; Reisa Kakubari; Tsuyoshi Hisa; Shoji Kamiura

Affiliations1. Department of Gynecology, Osaka International Cancer Institute, Osaka, Japan; 2. Department of Obstetrics and Gynecology, Ashiya Municipal Hospital, Hyogo, Japan

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SampleLatest 5 valid paper samples from 2026

Average review96.4 days

Median77 days

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