2199-5761

Balkan Journal of Medical Genetics

De Gruyter Poland Sp. z o.o.

View prefix report (10.2478)

Health Score

0 Good

Metadata coverage

Abstract
ORCID
References
License

Extended metadata coverage

Informational — signals of interoperability and funding across the corpus. Not part of the health score.

Funding

Funder
Award / grant

Affiliation & institutional identifiers

Affiliation
ROR ID

Update policy

Update policy

Your prioritized action plan

Ordered by how many DOIs each fix touches — start here, not with every error at once.

1

Attach ORCID iDs across 72 articles

ORCID iDs strengthen author disambiguation and institutional reporting.

High impact72 DOIs

DOIs for this ISSN

Showing the top 5 of 74 DOIs, ordered by correction priority.

# Title Missing Priority Citations
1 The Predisposition for Type 2 Diabetes Mellitus and Metaboli… (10.2478/bjmg-2023-0003)
ORCID
34.51 23
2 A New Clock is Running for Multiple Myeloma: Circadian Clock… (10.2478/bjmg-2022-0026)
ORCID
21.13 6
3 Rare and New Mutations of B-Globin in Azari Population of Ir… (10.2478/bjmg-2022-0016)
ORCID
19.45 5
4 Analysis of Mitochondrial Transfer RNA Mutations in Breast C… (10.2478/bjmg-2022-0020)
ORCID
19.45 5
5 <i>BRCA 1/BRCA 2</i> Pathogenic/Likely P… (10.2478/bjmg-2022-0023)
ORCID
19.45 5
6 Features of the Wolf-Hirschhorn Syndrome (WHS) from Infant t… (10.2478/bjmg-2023-0006)
ORCID
19.45 5
7 Comparison of FGF-8, FGF-10, FGF-Receptor 2, Androgen Recept… (10.2478/bjmg-2024-0002)
ORCID
19.45 5
8 High-Resolution HLA-DRB1 Allele Frequencies in a Romanian Co… (10.2478/bjmg-2024-0009)
ORCID
17.47 4
9 Epidermal Growth Factor Receptor Mutation Status and the Imp… (10.2478/bjmg-2022-0015)
ORCID
15.05 3
10 Adipocyte “Fatty Acid Binding Protein” Gene Polymorphisms (… (10.2478/bjmg-2022-0019)
ORCID
15.05 3
11 Congenital Hepatic Fibrosis as an Early Sign of Presentation… (10.2478/bjmg-2022-0024)
ORCID
15.05 3
12 Polyploidy Phenomenon as a Cause of Early Miscarriages in Ab… (10.2478/bjmg-2023-0002)
ORCID
15.05 3
13 Androgen Insensitivity Syndrome DUE to Non-Coding Variation… (10.2478/bjmg-2023-0012)
ORCID
15.05 3
14 Semilobar Holoprosencephaly Caused by a Novel and De Novo… (10.2478/bjmg-2022-0017)
ORCID
11.93 2
15 <i>SLC26A2</i> Related Diastrophic Dyspl… (10.2478/bjmg-2022-0018)
ORCID
11.93 2
16 High Risk of Gestational Trophoblastic Neoplasia Development… (10.2478/bjmg-2022-0025)
ORCID
11.93 2
17 Association of rs35006907 Polymorphism with Risk of Dilated… (10.2478/bjmg-2023-0004)
ORCID
11.93 2
18 Prognostic Value of <i>CYP1A2</i>… (10.2478/bjmg-2023-0005)
ORCID
11.93 2
19 Sensorineural Hearing Loss in a Child with Succinic Semialde… (10.2478/bjmg-2023-0008)
ORCID
11.93 2
20 Difficulties in Diagnosing Fabry Disease in Patients with Un… (10.2478/bjmg-2023-0010)
ORCID
11.93 2
21 Meaning and Clinical Interest of Minor Malformations and Nor… (10.2478/bjmg-2024-0010)
ORCID
11.93 2
22 Delineation of Partial Chromosomal Abnormalities in Early Pr… (10.2478/bjmg-2024-0014)
ORCID
11.93 2
23 Chromosomal Microarray in Children Born Small for Gestationa… (10.2478/bjmg-2024-0018)
ORCID
11.93 2
24 KDM3A, a Novel Blood-Based Biomarker in Colorectal Carcinoge… (10.2478/bjmg-2022-0021)
ORCID
7.53 1
25 Unusual Manifestation of Extraosseous Ewing Sarcoma: Report… (10.2478/bjmg-2022-0022)
ORCID
7.53 1
26 Molecular Characterization of Microrna Interference and Aris… (10.2478/bjmg-2022-0027)
ORCID
7.53 1
27 Non-Invasive Screening Test Paradox in a Case Born with Mixe… (10.2478/bjmg-2023-0007)
ORCID
7.53 1
28 Differentially Expressed Circulating Long-Noncoding RNAS in… (10.2478/bjmg-2023-0011)
ORCID
7.53 1
29 The Importance of Molecular Biological Analysis for the Labo… (10.2478/bjmg-2024-0001)
ORCID
7.53 1
30 The Spectrum and Frequency of Cystic Fibrosis Mutations in A… (10.2478/bjmg-2024-0004)
ORCID
7.53 1
31 Novel DGAT1 Mutations Identified in Congenital Diarrheal Dis… (10.2478/bjmg-2024-0005)
ORCID
7.53 1
32 The Impact of the COVID-19 Pandemic on Individuals with Down… (10.2478/bjmg-2024-0007)
ORCID
7.53 1
33 Ultra-Early Diffuse Lung Disease in an Infant with Pathogeni… (10.2478/bjmg-2024-0008)
ORCID
7.53 1
34 Association of <i>CYP2C19*2</i>… (10.2478/bjmg-2024-0015)
ORCID
7.53 1
35 Phenotypic Variability of Cowden Syndrome Within a Single Fa… (10.2478/bjmg-2024-0016)
ORCID
7.53 1
36 <i>Interleukin-1β</i> and… (10.2478/bjmg-2024-0017)
ORCID
7.53 1
37 Value of Optical Genome Mapping (OGM) for Diagnostics of Rar… (10.2478/bjmg-2024-0021)
ORCID
7.53 1
38 Qualitative and Quantitative Aspects of Discrepancies betwee… (10.2478/bjmg-2025-0009)
ORCID
7.53 1
39 Nephrotic Syndrome Induced by Tiopronin in a Male Patient wi… (10.2478/bjmg-2025-0012)
ORCID
7.53 1
40 Preventable Hazards from in Vitro Fertilization – A Case Ser… (10.2478/bjmg-2023-0001)
ORCID
0.00 0
41 Two Brothers from Macedonia with Gitelman Syndrome (10.2478/bjmg-2023-0009)
ORCID
0.00 0
42 IGHV Mutational Status in a Cohort of Bulgarian CLL Patients… (10.2478/bjmg-2024-0003)
ORCID
0.00 0
43 <i>ANXA5</i> and <i>… (10.2478/bjmg-2024-0006)
ORCID
0.00 0
44 A Pilot Study of <i>ANXA2, MED12, CALM1<… (10.2478/bjmg-2024-0011)
ORCID
0.00 0
45 In Vitro Analysis of AKR1D1 Interactions with Clopidogrel: E… (10.2478/bjmg-2024-0012)
ORCID
0.00 0
46 Investigation of TLR4 Polymorphism in Children with Vesicour… (10.2478/bjmg-2024-0013)
ORCID
0.00 0
47 Next-Generation Sequencing Infertility Panel in Turkey: Firs… (10.2478/bjmg-2024-0019)
0.00 1
48 <i>CREBBP</i> is a Major Prognostic Biom… (10.2478/bjmg-2024-0020)
ORCID
0.00 0
49 Novel <i>KIF11</i> V… (10.2478/bjmg-2025-0001)
ORCID
0.00 0
50 The Association of <i>ACSL1</i>… (10.2478/bjmg-2025-00015)
ORCID
0.00 0