Evidence map›Paper›PMID 37415649›Full record

ArticleEuropean journal of breast health2023

A Multicenter Study of Genotype Variation/Demographic Patterns in 2475 Individuals Including 1444 Cases With Breast Cancer in Turkey.

Ibrahim Boga, Sebnem Ozemri Sag, Nilgun Duman, Sevda Yesim Ozdemir, Mahmut Cerkez Ergoren, Kubilay Dalci, Cem Mujde, Cem Kaan Parsak, Cagla Rencuzogullari, Ozge Sonmezler and 27 more

Open access · diamondAbstract read
In one paragraph

Article in European journal of breast health, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Reclassification ofEuropean journal of breast health · 2025
    Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

37 authors at 8 institutions in 4 countries.

Ibrahim BogaCukurova University AGENTEM (Adana Genetic Diseases Diagnosis and Treatment Center), Adana, Turkey.ORCID https://orcid.org/0000-0002-8967-8218
Sebnem Ozemri SagDepartment of Medical Genetics and Genetic Diseases Diagnosis Center, Bursa Uludag University Faculty of Medicine, Bursa, Turkey.ORCID https://orcid.org/0000-0002-3948-8889
Nilgun DumanDepartment of Medical Genetics, Bezmialem Vakif University, Dragos Hospital, Istanbul, Turkey.ORCID https://orcid.org/0000-0003-0396-2240
Sevda Yesim OzdemirDepartment of Medical Genetics, Uskudar University Faculty of Medicine, Istanbul, Turkey.ORCID https://orcid.org/0000-0002-4398-2767
Mahmut Cerkez ErgorenDepartment of Medical Genetics, Near East University Faculty of Medicine, Nicosia, Cyprus.ORCID https://orcid.org/0000-0001-9593-9325
Kubilay DalciDepartment of General Surgery, Cukurova University Faculty of Medicine, Adana, Turkey.ORCID https://orcid.org/0000-0002-3156-4269
Cem MujdeCukurova University AGENTEM (Adana Genetic Diseases Diagnosis and Treatment Center), Adana, Turkey.ORCID https://orcid.org/0000-0002-7563-2948
Cem Kaan ParsakDepartment of General Surgery, Cukurova University Faculty of Medicine, Adana, Turkey.ORCID https://orcid.org/0000-0002-6515-8365
Cagla RencuzogullariCukurova University AGENTEM (Adana Genetic Diseases Diagnosis and Treatment Center), Adana, Turkey.ORCID https://orcid.org/0000-0003-4113-6820
Ozge SonmezlerCukurova University AGENTEM (Adana Genetic Diseases Diagnosis and Treatment Center), Adana, Turkey.ORCID https://orcid.org/0000-0002-2757-718X
Orcun YalavDepartment of General Surgery, Cukurova University Faculty of Medicine, Adana, Turkey.ORCID https://orcid.org/0000-0001-9239-4163
Adem AlemdarDepartment of Translational Medicine, Bursa Uludag University Institute of Health Sciences, Bursa, Turkey.ORCID https://orcid.org/0000-0003-3070-9224
Lamiya AliyevaDepartment of Medical Genetics and Genetic Diseases Diagnosis Center, Bursa Uludag University Faculty of Medicine, Bursa, Turkey.ORCID https://orcid.org/0000-0001-9436-9279
Ozlem BozkurtDepartment of Medical Pathology, Bursa Uludag University Faculty of Medicine, Bursa, Turkey.ORCID https://orcid.org/0000-0002-1282-9030
Sibel CetintasDepartment of Radiation Oncology, Bursa Uludag University Faculty of Medicine, Bursa, Turkey.ORCID https://orcid.org/0000-0002-4483-9284
Erdem CubukcuDepartment of Medical Oncology, Bursa Uludag University Faculty of Medicine, Bursa, Turkey.ORCID https://orcid.org/0000-0002-0070-0889
Adem DeligonulDepartment of Medical Oncology, Bursa Uludag University Faculty of Medicine, Bursa, Turkey.ORCID https://orcid.org/0000-0002-3669-6391
Berkcan DoganDepartment of Medical Genetics and Genetic Diseases Diagnosis Center, Bursa Uludag University Faculty of Medicine, Bursa, Turkey.ORCID https://orcid.org/0000-0001-8061-8131
Cemre Ornek ErguzelogluDepartment of Translational Medicine, Bursa Uludag University Institute of Health Sciences, Bursa, Turkey.ORCID https://orcid.org/0000-0002-5932-4259
Turkkan EvrenselDepartment of Translational Medicine, Bursa Uludag University Institute of Health Sciences, Bursa, Turkey.ORCID https://orcid.org/0000-0002-9732-5340
Sehsuvar GokgozDepartment of General Surgery, Bursa Uludag University Faculty of Medicine, Bursa, Turkey.ORCID https://orcid.org/0000-0003-1394-2630
Kazim SenolDepartment of General Surgery, Bursa Uludag University Faculty of Medicine, Bursa, Turkey.ORCID https://orcid.org/0000-0001-6273-0664
Sahsine TolunayDepartment of Medical Pathology, Bursa Uludag University Faculty of Medicine, Bursa, Turkey.ORCID https://orcid.org/0000-0002-9038-0515
Esra AkyurekDepartment of Medical Genetics, Erciyes University Faculty of Medicine, Kayseri, Turkey.ORCID https://orcid.org/0000-0003-0260-9904
Neslihan BasgozDepartment of Medical Genetics, Erciyes University Faculty of Medicine, Kayseri, Turkey.ORCID https://orcid.org/0000-0003-3567-5721
Nuriye GökçeDepartment of Medical Genetics, Erciyes University Faculty of Medicine, Kayseri, Turkey.ORCID https://orcid.org/0000-0001-7814-5224
Bilge DundarDepartment of Medical Genetics, Erciyes University Faculty of Medicine, Kayseri, Turkey.ORCID https://orcid.org/0000-0002-8553-8162
Figen OzturkDepartment of Pathology, Erciyes University Faculty of Medicine, Kayseri, Turkey.ORCID https://orcid.org/0000-0001-6180-5716
Duygu TaskinDepartment of Medical Genetics, Erciyes University Faculty of Medicine, Kayseri, Turkey.ORCID https://orcid.org/0000-0002-0279-257X
Mercan DemirtasMikrogen Genetic Diagnosis Laboratory, Ankara, Turkey.ORCID https://orcid.org/0009-0003-1562-5652
Murat CagDepartment of Vascular Surgery and Transplantation, Strasbourg University Nouvel Hospital, Strasbourg, France.ORCID https://orcid.org/0000-0003-4006-4079
Omer DikerDepartment of Medical Oncology, Near East University Faculty of Medicine, Nicosia, Cyprus.ORCID https://orcid.org/0000-0001-7162-4812
Polat OlgunDepartment of Medical Oncology, Near East University Faculty of Medicine, Nicosia, Cyprus.ORCID https://orcid.org/0000-0001-8572-4304
Sevcan Tug BozdoganCukurova University AGENTEM (Adana Genetic Diseases Diagnosis and Treatment Center), Adana, Turkey.ORCID https://orcid.org/0000-0001-8572-4304
Munis DundarDepartment of Medical Genetics, Erciyes University Faculty of Medicine, Kayseri, Turkey.ORCID https://orcid.org/0000-0003-0969-4611
Atil BisginCukurova University AGENTEM (Adana Genetic Diseases Diagnosis and Treatment Center), Adana, Turkey.ORCID https://orcid.org/0000-0002-2053-9076
Sehime Gulsun TemelDepartment of Medical Genetics and Genetic Diseases Diagnosis Center, Bursa Uludag University Faculty of Medicine, Bursa, Turkey.ORCID https://orcid.org/0000-0002-9802-0880
Bursa Uludağ Üni̇versi̇tesi̇ · TRCukurova University · TRErciyes University · TRNear East University · CYBezmiâlem Vakıf Üniversitesi · TRHôpital Civil, Strasbourg · FRUniversity of Iowa · USÜsküdar University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Breast cancer (BC) is the most common cancer type in women and may be inherited, mostly in an autosomal dominant pattern. The clinical diagnosis of BC relies on the published diagnostic criteria, and analysis of two genes, Materials and Methods: Mutational analyses for the Results: Overall, mutations were identified in 17% (421/2475), while the percentage of mutation carriers in cases of BC was similar, 16.6% (239/1444). Conclusion: Patients with

Indexed as

BRCA1BRCA2Breast cancergenomic profilingpopulation study

Identifiers

PMID37415649
PMCPMC10320635
OpenAlexW4382982138

What OpenQuestion holds

Textmetadata
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.