Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

B. Pasini · SciRah

Researcher profile · Semantic Scholar

B. Pasini

Share profile

B. Pasini — researcher profile on SciRah

h-index: 52
Works: 143
Citations: 15K

Most-cited papers

Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
N. Mavaddat, D. Barrowdale, I. Andrulis, S. Domchek +129 more
2011Cancer Epidemiology, Biomarkers and Prevention599 citations Open access
Semantic Scholar
Clinical and molecular genetics of patients with the Carney–Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD
B. Pasini, S. Mcwhinney, Thalia A. Bei, L. Matyakhina +15 more
2008European Journal of Human Genetics473 citations
Semantic Scholar
Recurrent somatic DICER1 mutations in nonepithelial ovarian cancers.
A. Heravi-Moussavi, M. Anglesio, S. Cheng, J. Senz +30 more
2012New England Journal of Medicine472 citations Open access
Semantic Scholar
Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations
T. Rebbeck, T. Friebel, E. Friedman, U. Hamann +238 more
2018Human Mutation299 citations Open access
Semantic Scholar
Does chromosome 17 centromere copy number predict polysomy in breast cancer? A fluorescence in situ hybridization and microarray‐based CGH analysis
C. Marchiò, M. Lambros, P. Gugliotta, L. D. di Cantogno +10 more
2009Journal of Pathology216 citations Open access
Semantic Scholar
Familial gastrointestinal stromal tumors and germ-line mutations.
S. Mcwhinney, B. Pasini, C. Stratakis
2007New England Journal of Medicine214 citations Open access
Semantic Scholar
Extending the phenotypes associated with DICER1 mutations
W. Foulkes, A. Bahubeshi, N. Hamel, B. Pasini +15 more
2011Human Mutation200 citations Open access
Semantic Scholar
Rapid progression of prostate cancer in men with a BRCA2 mutation
S. Narod, S. Neuhausen, G. Vichodez, S. Armel +35 more
2008British Journal of Cancer167 citations Open access
Semantic Scholar
Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma
J. Bayley, Ivonne van Minderhout, M. Weiss, J. Jansen +10 more
2006BMC Medical Genetics156 citations Open access
Semantic Scholar
Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies
A. Antoniou, P. Pharoah, S. Narod, H. Risch +28 more
2005Journal of Medical Genetics153 citations Open access
Semantic Scholar
Succinate dehydrogenase (SDH) D subunit (SDHD) inactivation in a growth-hormone-producing pituitary tumor: a new association for SDH?
P. Xekouki, K. Pacak, M. Almeida, C. Wassif +15 more
2012Journal of Clinical Endocrinology and Metabolism152 citations Open access
Semantic Scholar
Genetics of carney triad: recurrent losses at chromosome 1 but lack of germline mutations in genes associated with paragangliomas and gastrointestinal stromal tumors.
L. Matyakhina, Thalia A. Bei, S. Mcwhinney, B. Pasini +17 more
2007Journal of Clinical Endocrinology and Metabolism152 citations
Semantic Scholar
Association of Type and Location of BRCA1 and BRCA2 Mutations With Risk of Breast and Ovarian Cancer
T. Rebbeck, N. Mitra, F. Wan, O. Sinilnikova +252 more
2015Journal of the American Medical Association (JAMA)147 citations Open access
Semantic Scholar
Incidental Carcinomas in Prophylactic Specimens in BRCA1 and BRCA2 Germ-line Mutation Carriers, With Emphasis on Fallopian Tube Lesions: Report of 6 Cases and Review of the Literature
M. Carcangiu, B. Peissel, B. Pasini, G. Spatti +2 more
2006American Journal of Surgical Pathology131 citations
Semantic Scholar
Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia
A. Spurdle, F. Couch, M. Parsons, L. McGuffog +189 more
2014Breast Cancer Research119 citations Open access
Semantic Scholar
Infertility, treatment of infertility, and the risk of breast cancer among women with BRCA1 and BRCA2 mutations: a case–control study
J. Kotsopoulos, C. Librach, J. Lubiński, J. Gronwald +13 more
2008Cancer Causes and Control117 citations
Semantic Scholar
Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2
Valentina Silvestri, D. Barrowdale, A. Mulligan, S. Neuhausen +142 more
2016Breast Cancer Research111 citations Open access
Semantic Scholar
Prevalence of Hypokalemia and Primary Aldosteronism in 5100 Patients Referred to a Tertiary Hypertension Unit
J. Burrello, S. Monticone, I. Losano, Giovanni Cavaglià +8 more
2020HYPERTENSION106 citations Open access
Semantic Scholar
Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2
A. Mulligan, F. Couch, D. Barrowdale, S. Domchek +186 more
2011Breast Cancer Research102 citations Open access
Semantic Scholar
Liddle Syndrome: Review of the Literature and Description of a New Case
M. Tetti, S. Monticone, J. Burrello, P. Matarazzo +4 more
2018International Journal of Molecular Sciences94 citations Open access
Semantic Scholar
Germline mutations in DNA repair genes predispose asbestos-exposed patients to malignant pleural mesothelioma.
M. Betti, E. Casalone, D. Ferrante, A. Aspesi +17 more
2017Cancer Letters89 citations Open access
Semantic Scholar
Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers.
A. Antoniou, Christiana Kartsonaki, O. Sinilnikova, P. Soucy +175 more
2011Human Molecular Genetics84 citations Open access
Semantic Scholar
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers.
Huong D. Meeks, Hong-Lin Song, K. Michailidou, M. Bolla +249 more
2016Journal of the National Cancer Institute82 citations Open access
Semantic Scholar
Association of a new cationic trypsinogen gene mutation (V39A) with chronic pancreatitis in an Italian family
C. Arduino, P. Salacone, B. Pasini, A. Brusco +8 more
2005Gut70 citations Open access
Semantic Scholar
Recommendations for the implementation of BRCA testing in ovarian cancer patients and their relatives.
S. Gori, M. Barberis, M. Bella, F. Buttitta +25 more
2019Critical reviews in oncology/hematology63 citations Open access
Semantic Scholar
PARP1 expression drives the synergistic antitumor activity of trabectedin and PARP1 inhibitors in sarcoma preclinical models
Y. Pignochino, F. Capozzi, L. D'Ambrosio, C. Dell'aglio +18 more
2017Molecular Cancer62 citations Open access
Semantic Scholar
Sensitivity to asbestos is increased in patients with mesothelioma and pathogenic germline variants in BAP1 or other DNA repair genes
M. Betti, A. Aspesi, D. Ferrante, Marika Sculco +21 more
2018Genes, Chromosomes and Cancer61 citations
Semantic Scholar
Multiple gastrointestinal stromal and other tumors caused by platelet-derived growth factor receptor alpha gene mutations: a case associated with a germline V561D defect.
B. Pasini, L. Matyakhina, Thalia A. Bei, M. Muchow +4 more
2007Journal of Clinical Endocrinology and Metabolism59 citations
Semantic Scholar
Treatment of infertility does not increase the risk of ovarian cancer among women with a BRCA1 or BRCA2 mutation.
J. Gronwald, K. Glass, B. Rosen, B. Karlan +76 more
2016Fertility and Sterility56 citations Open access
Semantic Scholar
Implementation of preventive and predictive BRCA testing in patients with breast, ovarian, pancreatic, and prostate cancer: a position paper of Italian Scientific Societies
A. Russo, L. Incorvaia, E. Capoluongo, P. Tagliaferri +64 more
2022ESMO Open54 citations Open access
Semantic Scholar
Age at first birth and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers
J. Kotsopoulos, J. Lubiński, H. Lynch, J. Klijn +40 more
2007Breast Cancer Research and Treatment54 citations
Semantic Scholar
The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries
Y. Laitman, T. Friebel, D. Yannoukakos, F. Fostira +32 more
2019Human Mutation49 citations Open access
Semantic Scholar
Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes
E. di Gregorio, E. Riberi, E. Belligni, E. Biamino +39 more
2017Clinical Genetics47 citations Open access
Semantic Scholar
Clinical genetic testing for familial melanoma in Italy: a cooperative study.
W. Bruno, P. Ghiorzo, L. Battistuzzi, P. Ascierto +23 more
2009Journal of American Academy of Dermatology47 citations Open access
Semantic Scholar
GENETICS IN ENDOCRINOLOGY: The expanding genetic horizon of primary aldosteronism.
S. Monticone, F. Buffolo, M. Tetti, F. Veglio +2 more
2018European Journal of Endocrinology44 citations Open access
Semantic Scholar
Differences and homologies of chromosomal alterations within and between breast cancer cell lines: a clustering analysis
Milena Rondón-Lagos, Ludovica Verdun di Cantogno, C. Marchiò, N. Rangel +7 more
2014Molecular Cytogenetics44 citations Open access
Semantic Scholar
A Comparison of Bilateral Breast Cancers in BRCA Carriers
J. Weitzel, M. Robson, B. Pasini, S. Manoukian +15 more
2005Cancer Epidemiology, Biomarkers and Prevention44 citations
Semantic Scholar
Predictors of recurrence of pheochromocytoma and paraganglioma: a multicenter study in Piedmont, Italy
M. Parasiliti-Caprino, B. Lucatello, Chiara Lopez, J. Burrello +26 more
2019Hypertension Research42 citations Open access
Semantic Scholar
Ovarian cancer in BRCA1 and BRCA2 gene mutation carriers: analysis of prognostic factors and survival
N. Biglia, P. Sgandurra, V. Bounous, F. Maggiorotto +4 more
2016ecancermedicalscience34 citations Open access
Semantic Scholar
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants
Hong-Yan Li, C. Engel, M. de la Hoya, P. Peterlongo +57 more
2021Genetics in Medicine31 citations Open access
Semantic Scholar
Mutational screening of the RB1 gene in Italian patients with retinoblastoma reveals 11 novel mutations
K. Sampieri, T. Hadjistilianou, F. Mari, Caterina Speciale +11 more
2006Journal of Human Genetics30 citations
Semantic Scholar
Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genes
Chiara Giovenino, S. Trajkova, Lisa Pavinato, S. Cardaropoli +25 more
2023European Journal of Human Genetics26 citations Open access
Semantic Scholar
The expression of LINE1‐MET chimeric transcript identifies a subgroup of aggressive breast cancers
U. Miglio, E. Berrino, M. Panero, G. Ferrero +11 more
2018International Journal of Cancer26 citations Open access
Semantic Scholar
Exploring the link between MORF4L1 and risk of breast cancer
Griselda Martrat, C. Maxwell, Emiko Tominaga, Montserrat Porta-de-la-Riva +130 more
2011Breast Cancer Research26 citations Open access
Semantic Scholar
20 novel point mutations and one large deletion in EXT1 and EXT2 genes: report of diagnostic screening in a large Italian cohort of patients affected by hereditary multiple exostosis.
M. Ciavarella, M. Coco, Filomena Baorda, P. Stanziale +15 more
2013Gene25 citations
Semantic Scholar
Recommendations for the implementation of BRCA testing in the care and treatment pathways of ovarian cancer patients.
C. Pinto, M. Bella, E. Capoluongo, Paola Carrera +20 more
2016Future Oncology24 citations Open access
Semantic Scholar
A large de novo 9p21.3 deletion in a girl affected by astrocytoma and multiple melanoma
S. Frigerio, Vittoria Disciglio, S. Manoukian, B. Peissel +9 more
2014BMC Medical Genetics24 citations Open access
Semantic Scholar
Radiofrequency Ablation for Renal Cancer in Von Hippel–Lindau Syndrome Patients: A Prospective Cohort Analysis
M. Allasia, F. Soria, A. Battaglia, C. Gazzera +9 more
2017Clinical Genitourinary Cancer23 citations
Semantic Scholar
Mutation detection rates associated with specific selection criteria for BRCA1/2 testing in 1854 high-risk families: A monocentric Italian study.
J. Azzollini, G. Scuvera, E. Bruno, P. Pasanisi +9 more
2016European journal of internal medicine22 citations
Semantic Scholar
TERT Promoter Mutations are Associated with Visceral Spreading in Melanoma of the Trunk
S. Osella-Abate, L. Bertero, R. Senetta, S. Mariani +11 more
2019Cancers20 citations Open access
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

S. Manoukian×21
Invite
S. Manoukian — researcher profile on SciRah
P. Radice×15
Invite
P. Radice — researcher profile on SciRah
S. Domchek×12
Invite
S. Domchek — researcher profile on SciRah
B. Peissel×12
Invite
B. Peissel — researcher profile on SciRah

×12

Invite

S. Neuhausen — researcher profile on SciRah

Invite

N. Tung — researcher profile on SciRah

G. Chenevix-Trench×11

Invite

G. Chenevix-Trench — researcher profile on SciRah

A. Antoniou×11

Invite

A. Antoniou — researcher profile on SciRah

H. Nevanlinna×10

Invite

H. Nevanlinna — researcher profile on SciRah

Invite

F. Couch — researcher profile on SciRah

L. McGuffog×10

Invite

L. McGuffog — researcher profile on SciRah

Invite

D. Goldgar — researcher profile on SciRah