1755-8166

Molecular Cytogenetics

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DOIs for this ISSN

Showing the top 5 of 1182 DOIs, ordered by correction priority.

# Title Missing Priority Citations
1 Chromosomal mosaicism goes global (10.1186/1755-8166-1-26)
Abstract References ORCID License
206.82 116
2 Cytogenetic contribution to uniparental disomy (UPD) (10.1186/1755-8166-3-8)
Abstract References ORCID License
205.69 113
3 On the origin of trisomy 21 Down syndrome (10.1186/1755-8166-1-21)
Abstract References ORCID License
181.95 65
4 GIN'n'CIN hypothesis of brain aging: deciphering the role of… (10.1186/1755-8166-2-23)
Abstract References ORCID License
173.24 53
5 Fluorescence in situ hybridization in combination with the c… (10.1186/1755-8166-3-17)
Abstract References ORCID License
173.24 53
6 Small supernumerary marker chromosomes (sSMC) in humans; are… (10.1186/1755-8166-1-12)
Abstract References ORCID License
156.82 36
7 Chromosome aberrations in a large series of spontaneous misc… (10.1186/1755-8166-7-38)
Abstract References ORCID License
151.85 32
8 Diagnostic utility of novel combined arrays for genome-wide… (10.1186/1755-8166-7-43)
Abstract References ORCID License
150.51 31
9 An easy “SteamDrop” method for high quality plant chromosome… (10.1186/1755-8166-7-21)
Abstract ORCID License
149.34 97
10 X chromosome aneuploidy in the Alzheimer’s disease brain (10.1186/1755-8166-7-20)
Abstract ORCID License
147.98 93
11 Evaluation of three read-depth based CNV detection tools usi… (10.1186/s13039-017-0333-5)
Abstract ORCID License
146.20 88
12 8p23.1 duplication syndrome differentiated from copy number… (10.1186/1755-8166-3-3)
Abstract References ORCID License
144.72 27
13 Unexpected structural complexity of supernumerary marker chr… (10.1186/1755-8166-1-7)
Abstract References ORCID License
141.50 25
14 Juxtaposition of heterochromatic and euchromatic regions by… (10.1186/1755-8166-5-16)
Abstract References ORCID License
141.50 25
15 Low grade mosaic for a complex supernumerary ring chromosome… (10.1186/1755-8166-3-13)
Abstract References ORCID License
139.79 24
16 On the paternal origin of trisomy 21 Down syndrome (10.1186/1755-8166-3-4)
Abstract References ORCID License
139.79 24
17 Germ-line transmission of trisomy 21: Data from 80 families… (10.1186/1755-8166-3-7)
Abstract References ORCID License
139.79 24
18 Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinica… (10.1186/1755-8166-1-18)
Abstract References ORCID License
138.02 23
19 MLPA for confirmation of array CGH results and determination… (10.1186/1755-8166-3-19)
Abstract References ORCID License
138.02 23
20 6p22.3 deletion: report of a patient with autism, severe int… (10.1186/1755-8166-6-4)
Abstract References ORCID License
138.02 23
21 Chromosome distribution in human sperm – a 3D multicolor ban… (10.1186/1755-8166-1-25)
Abstract ORCID License
137.44 67
22 Exosome-delivered microRNAs of “chromosome 19 microRNA clust… (10.1186/1755-8166-5-27)
Abstract ORCID License
136.96 66
23 Genomic SNP array as a gold standard for prenatal diagnosis… (10.1186/1755-8166-5-14)
Abstract ORCID License
136.47 65
24 A novel deletion in proximal 22q associated with cardiac sep… (10.1186/1755-8166-2-9)
Abstract References ORCID License
136.17 22
25 Selection of single blastocysts for fresh transfer via stand… (10.1186/1755-8166-5-24)
ORCID License
133.97 477
26 Identification of mosaic and segmental aneuploidies by next-… (10.1186/s13039-017-0315-7)
Abstract ORCID License
132.81 58
27 Segmental paleotetraploidy revealed in sterlet (Acipenser ru… (10.1186/s13039-015-0194-8)
Abstract ORCID License
131.69 56
28 Array CGH as a first line diagnostic test in place of karyot… (10.1186/1755-8166-6-16)
Abstract ORCID License
127.42 49
29 Why it is crucial to analyze non clonal chromosome aberratio… (10.1186/s13039-016-0223-2)
Abstract ORCID License
126.76 48
30 Karyotypic analysis and FISH mapping of microsatellite motif… (10.1186/1755-8166-6-60)
Abstract ORCID License
124.71 45
31 Early detection and personalized treatment in oral cancer: t… (10.1186/s13039-016-0293-1)
Abstract ORCID License
124.71 45
32 Molecular karyotyping by array CGH in a Russian cohort of ch… (10.1186/1755-8166-5-46)
Abstract ORCID License
123.99 44
33 Chromosomal microarray analysis in the genetic evaluation of… (10.1186/s13039-018-0363-7)
Abstract ORCID License
123.99 44
34 The use of array-CGH in a cohort of Greek children with deve… (10.1186/1755-8166-3-22)
Abstract References ORCID License
123.04 16
35 Genomic imbalances pinpoint potential oncogenes and tumor su… (10.1186/s13039-016-0227-y)
Abstract ORCID License
120.96 40
36 Genomic amplification of BCR/ABL1 and a region downstream of… (10.1186/1755-8166-3-15)
Abstract References ORCID License
120.41 15
37 Differences and homologies of chromosomal alterations within… (10.1186/1755-8166-7-8)
Abstract ORCID License
120.15 39
38 Chromosomal copy number analysis on chorionic villus samples… (10.1186/s13039-015-0210-z)
Abstract ORCID License
120.15 39
39 Intragenic deletion of RBFOX1 associated with neurodevelopme… (10.1186/1755-8166-6-26)
Abstract ORCID License
119.33 38
40 Selection of euploid blastocysts for cryopreservation with a… (10.1186/1755-8166-6-32)
Abstract ORCID License
119.33 38
41 Abnormalities in spontaneous abortions detected by G-banding… (10.1186/1755-8166-7-33)
Abstract ORCID License
119.33 38
42 Incidence of the 22q11.2 deletion in a large cohort of misca… (10.1186/s13039-017-0308-6)
Abstract ORCID License
119.33 38
43 Noninvasive prenatal diagnosis of fetal aneuploidy by circul… (10.1186/s13039-017-0343-3)
Abstract ORCID License
119.33 38
44 Genetic testing for hearing loss in the United States should… (10.1186/1755-8166-6-19)
Abstract ORCID License
118.48 37
45 Inherent variability of cancer-specific aneuploidy generates… (10.1186/s13039-016-0297-x)
Abstract ORCID License
118.48 37
46 Monitoring of gas station attendants exposure to benzene, to… (10.1186/1755-8166-7-15)
Abstract ORCID License
117.62 36
47 Assessment of ERBB2 and EGFR gene amplification and protein… (10.1186/1755-8166-4-14)
Abstract ORCID License
115.81 34
48 Complex small supernumerary marker chromosomes – an update (10.1186/1755-8166-6-46)
Abstract ORCID License
115.81 34
49 Chromosome 22q11.2 microdeletion in monozygotic twins with d… (10.1186/1755-8166-5-13)
Abstract ORCID License
114.86 33
50 Genome profiling of ovarian adenocarcinomas using pangenomic… (10.1186/1755-8166-1-10)
Abstract References ORCID License
114.61 13