LIG Audit Status

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Batch audit-20260421-labels-seed42 · created 2026-04-21 07:03 · seed 42

caucasian
25 reviewed / 25 total
0 pending
Confirmed caucasian 25 · Not caucasian on review 0
white
25 reviewed / 25 total
0 pending
Confirmed white 24 · Not white on review 1
european
10 reviewed / 25 total
15 pending
Confirmed european 10 · Not european on review 0
other
25 reviewed / 25 total
0 pending
Confirmed other 25 · Not other on review 0
none of these labels
0 reviewed / 100 total
100 pending
Confirmed none of these labels 0 · Uses tracked labels on review 0

["Announcement"]

European Journal of Human Genetics · 1996 · article 70112664 · 10.1159/000472219

Review target: none of these labels. Review status: pending

Audit result: pending

Classifier flags: none

No abstract available.
Target Article Journal Status Outcome Reviewer Updated
none of these labels ["Correction: Ethical and public health implications of genetic testing for suicide risk: family and survivor perspectives"]
article 38635275
Genetics in Medicine
2021
pending pending 2026-04-21 07:03
none of these labels ["Issue Information"]
article 49975058
Journal of Genetic Counseling
2019
pending pending 2026-04-21 07:03
none of these labels ["Fetal bowel hyperechogenicity may indicate mild atypical cystic fibrosis: a case associated with a complex CFTR allele"]
article 53388855
Journal of Medical Genetics
2000
pending pending 2026-04-21 07:03
none of these labels ["Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways"]
article 53595520
The American Journal of Human Genetics
2019
pending pending 2026-04-21 07:03
none of these labels ["Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for <i>FOXA2</i> in 20p11.2 deletion syndrome"]
article 54149971
American Journal of Medical Genetics Part A
2019
pending pending 2026-04-21 07:03
none of these labels ["A local score approach improves GWAS resolution and detects minor QTL: application to Medicago truncatula quantitative disease resistance to multiple Aphanomyces euteiches isolates"]
article 55371035
Heredity
2019
pending pending 2026-04-21 07:03
none of these labels ["A glycine transporter SLC6A5 frameshift mutation causes startle disease in Spanish greyhounds"]
article 57520254
Human Genetics
2019
pending pending 2026-04-21 07:03
none of these labels ["Correction: Patient experience and utility of genetic information: a cross-sectional study among patients tested for cancer susceptibility and thrombophilia"]
article 63525563
European Journal of Human Genetics
2018
pending pending 2026-04-21 07:03
none of these labels ["Estimating Causal Effects on a Disease Progression Trait Using Bivariate Mendelian Randomisation"]
article 68050007
Genetic Epidemiology
2024
pending pending 2026-04-21 07:03
none of these labels ["The genetic architecture of ecological adaptation: intraspecific variation in host plant use by the lepidopteran crop pest Chloridea virescens"]
article 68860950
Heredity
2017
pending pending 2026-04-21 07:03
none of these labels ["Syndactylies and Polydactylies:\nEmbryological Overview and\nSuggested Classification"]
article 70102757
European Journal of Human Genetics
1993
pending pending 2026-04-21 07:03
none of these labels ["Announcement"]
article 70112664
European Journal of Human Genetics
1996
pending pending 2026-04-21 07:03
none of these labels ["Detection of homozygous deletions in tumor‐suppressor genes ranging from dozen to hundreds nucleotides in cancer models"]
article 72005142
Human Mutation
2017
pending pending 2026-04-21 07:03
none of these labels ["Bullous Lung Disease in Turner Syndrome: An Underrecognized Comorbidity?"]
article 72215019
American Journal of Medical Genetics Part A
2024
pending pending 2026-04-21 07:03
none of these labels ["Automatic recognition of the <scp>XLHED</scp> phenotype from facial images"]
article 72589974
American Journal of Medical Genetics Part A
2017
pending pending 2026-04-21 07:03
none of these labels ["The Genetic Architecture of Gene Expression in Peripheral Blood"]
article 76575307
The American Journal of Human Genetics
2017
pending pending 2026-04-21 07:03
none of these labels ["Epidemiology of neurofibromatosis type 1 (NF1) in northern Finland"]
article 79499278
Journal of Medical Genetics
2000
pending pending 2026-04-21 07:03
none of these labels ["Novel Clinical Manifestation and Favorable Treatment Outcome of Cochlear Implant in a Chinese Family With Likely Pathogenic Variant of the <scp><i>P2RX2</i></scp> Gene"]
article 82329988
American Journal of Medical Genetics Part A
2024
pending pending 2026-04-21 07:03
none of these labels ["Metatropic dysplasia is associated with increased fracture risk"]
article 84944978
American Journal of Medical Genetics Part A
2016
pending pending 2026-04-21 07:03
none of these labels ["Screening of the BRCA1 gene in Brazilian patients with breast and/or ovarian cancer via high-resolution melting reaction analysis"]
article 85895646
Familial Cancer
2015
pending pending 2026-04-21 07:03
none of these labels ["Mothers’ psychological adaptation to Duchenne/Becker muscular dystrophy"]
article 88090577
European Journal of Human Genetics
2015
pending pending 2026-04-21 07:03
none of these labels ["Acceptability of, and Information Needs Regarding, Next‐Generation Sequencing in People Tested for Hereditary Cancer: A Qualitative Study"]
article 88355411
Journal of Genetic Counseling
2015
pending pending 2026-04-21 07:03
none of these labels ["RASopathy-Associated<i>CBL</i>Germline Mutations Cause Aberrant Ubiquitylation and Trafficking of EGFR"]
article 95375132
Human Mutation
2014
pending pending 2026-04-21 07:03
none of these labels ["Application of an ordered subset analysis approach to the genetics of alcoholism"]
article 100875099
Genetic Epidemiology
1999
pending pending 2026-04-21 07:03
none of these labels ["Standard enrichment methods for targeted next-generation sequencing in high-repeat genomic regions"]
article 101341710
Genetics in Medicine
2013
pending pending 2026-04-21 07:03
none of these labels ["Extremely reduced dispersal and gene flow in an island bird"]
article 102141345
Heredity
2013
pending pending 2026-04-21 07:03
none of these labels ["Newborn bloodspot screening for Duchenne Muscular Dystrophy: 21 years experience in Wales (UK)"]
article 107196477
European Journal of Human Genetics
2013
pending pending 2026-04-21 07:03
none of these labels ["Length Distributions of Identity by Descent Reveal Fine-Scale Demographic History"]
article 108236249
The American Journal of Human Genetics
2012
pending pending 2026-04-21 07:03
none of these labels ["Recommendations for using standardised phenotypes in genetic association studies"]
article 110698605
Human Genomics
2009
pending pending 2026-04-21 07:03
none of these labels ["Analysis of pharmacogenetic traits in two distinct South African populations"]
article 110871826
Human Genomics
2011
pending pending 2026-04-21 07:03
none of these labels ["Rare<i>TP53</i>genetic variant associated with glioma risk and outcome"]
article 111323771
Journal of Medical Genetics
2012
pending pending 2026-04-21 07:03
none of these labels ["<i>KRAS</i> gene mutations in Noonan syndrome familial cases cluster in the vicinity of the switch II region of the G‐domain: Report of another family with metopic craniosynostosis"]
article 112590088
American Journal of Medical Genetics Part A
2012
pending pending 2026-04-21 07:03
none of these labels ["Peroxisomal Disorders"]
article 115660998
Human Genetics
1987
pending pending 2026-04-21 07:03
none of these labels ["Skipping along: an exon skipping therapy shows promise for Duchenne muscular dystrophy"]
article 118083471
Clinical Genetics
2011
pending pending 2026-04-21 07:03
none of these labels ["Haploinsufficiency of HDAC4 Causes Brachydactyly Mental Retardation Syndrome, with Brachydactyly Type E, Developmental Delays, and Behavioral Problems"]
article 124500845
The American Journal of Human Genetics
2010
pending pending 2026-04-21 07:03
none of these labels ["Catechol‐O‐methyltransferase activity in erythrocytes in Down's syndrome"]
article 124860947
Clinical Genetics
1973
pending pending 2026-04-21 07:03
none of these labels ["Intracellular retention of lysosomal enzymes in cystic fibrosis"]
article 124861823
Clinical Genetics
1981
pending pending 2026-04-21 07:03
none of these labels ["Diagnosis of cystic fibrosis homozygotes and heterozygotes from plasma and fibroblast cultures. A three‐generation family study"]
article 124901338
Clinical Genetics
1983
pending pending 2026-04-21 07:03
none of these labels ["Fitzsimmons syndrome: Spastic paraplegia, brachydactyly and cognitive impairment"]
article 129560030
American Journal of Medical Genetics Part A
2009
pending pending 2026-04-21 07:03
none of these labels ["The multidimensionality of schizotypy in nonpsychotic relatives of patients with schizophrenia and its applications in ordered subsets linkage analysis of schizophrenia"]
article 131605007
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
2009
pending pending 2026-04-21 07:03
none of these labels ["Minute Y chromosome derived marker in a child with gonadoblastoma: cytogenetic and DNA studies."]
article 134016697
Journal of Medical Genetics
1992
pending pending 2026-04-21 07:03
none of these labels ["Cystic fibrosis screening and community genetics."]
article 134021707
Journal of Medical Genetics
1990
pending pending 2026-04-21 07:03
none of these labels ["DiGeorge syndrome: an historical review of clinical and cytogenetic features."]
article 134021826
Journal of Medical Genetics
1993
pending pending 2026-04-21 07:03
none of these labels ["Dermatoglyphic findings in Poland's syndrome."]
article 134031330
Journal of Medical Genetics
1980
pending pending 2026-04-21 07:03
none of these labels ["Lancelot Hogben Scientific Humanist. An Unauthorised Autobiography"]
article 134032117
Journal of Medical Genetics
1998
pending pending 2026-04-21 07:03
none of these labels ["Genetical components of physiological tremor."]
article 134041195
Journal of Medical Genetics
1975
pending pending 2026-04-21 07:03
none of these labels ["Medical genetics: advances in brief: An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia"]
article 134041990
Journal of Medical Genetics
1998
pending pending 2026-04-21 07:03
none of these labels ["Partial 12p deletion: a cause for a mental retardation, multiple congenital abnormality syndrome."]
article 134047620
Journal of Medical Genetics
1975
pending pending 2026-04-21 07:03
none of these labels ["Survivors of neuroblastoma and ganglioneuroma and their families."]
article 134047697
Journal of Medical Genetics
1982
pending pending 2026-04-21 07:03
none of these labels ["Fungal mating-types"]
article 136573065
Heredity
1967
pending pending 2026-04-21 07:03
none of these labels ["The genetics of the bee-like patterns of Merodon equestris"]
article 136573315
Heredity
1972
pending pending 2026-04-21 07:03
none of these labels ["Failure to transmit mutant plastids in a pelargonium cross"]
article 136577838
Heredity
1964
pending pending 2026-04-21 07:03
none of these labels ["Variability of outcrossing frequency in Senecio vulgaris L."]
article 136751673
Heredity
1976
pending pending 2026-04-21 07:03
none of these labels ["Reviews"]
article 136751708
Heredity
1977
pending pending 2026-04-21 07:03
none of these labels ["B chromosome selection and fitness in rye"]
article 136756852
Heredity
1978
pending pending 2026-04-21 07:03
none of these labels ["One- and two-sample tests for single-locus inbreeding coefficients using the bootstrap"]
article 137081944
Heredity
1995
pending pending 2026-04-21 07:03
none of these labels ["Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type II"]
article 137550126
Human Mutation
2008
pending pending 2026-04-21 07:03
none of these labels ["Pituitary hypoplasia and growth hormone deficiency in Coffin‐Siris syndrome"]
article 137944981
American Journal of Medical Genetics Part A
2008
pending pending 2026-04-21 07:03
none of these labels ["This Month in the Journal"]
article 138708120
The American Journal of Human Genetics
2007
pending pending 2026-04-21 07:03
none of these labels ["Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease"]
article 138825286
The American Journal of Human Genetics
2024
pending pending 2026-04-21 07:03
none of these labels ["Neuropathy as a presenting feature in fragile X‐associated tremor/ataxia syndrome"]
article 140115125
American Journal of Medical Genetics Part A
2007
pending pending 2026-04-21 07:03
none of these labels ["Clinical features in adults with congenital disorders of glycosylation type Ia (CDG‐Ia)"]
article 140554952
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
2007
pending pending 2026-04-21 07:03
none of these labels ["Ambulatory electrocardiogram analysis in infants treated with recombinant human acid α-glucosidase enzyme replacement therapy for Pompe disease"]
article 148730511
Genetics in Medicine
2006
pending pending 2026-04-21 07:03
none of these labels ["Perceptions and Attitudes about <i>HFE</i> Genotyping Among College‐Age Adults"]
article 151061825
Journal of Genetic Counseling
2005
pending pending 2026-04-21 07:03
none of these labels ["Cardiovascular malformations in Fryns syndrome: Is there a pathogenic role for neural crest cells?"]
article 151579983
American Journal of Medical Genetics Part A
2005
pending pending 2026-04-21 07:03
none of these labels ["Novel frameshift mutation in exon 4 of CFTR gene"]
article 153591575
Human Mutation
1995
pending pending 2026-04-21 07:03
none of these labels ["Masthead"]
article 153596292
Genetic Epidemiology
1992
pending pending 2026-04-21 07:03
none of these labels ["Announcements"]
article 154373265
Journal of Genetic Counseling
1994
pending pending 2026-04-21 07:03
none of these labels ["Identification of a novel mevalonate kinase gene mutation in combination with the common MVK V377I substitution and the low-penetrance TNFRSF1A R92Q mutation"]
article 155883917
European Journal of Human Genetics
2004
pending pending 2026-04-21 07:03
none of these labels ["Congenital hyperinsulinism: Molecular basis of a heterogeneous disease"]
article 157296455
Human Mutation
1999
pending pending 2026-04-21 07:03
none of these labels ["Familial benign hypercalcaemia (FBH; McK. No. 14598, 1983): Linkage studies in a large Dutch family"]
article 157866536
Human Genetics
1984
pending pending 2026-04-21 07:03
none of these labels ["Syndrome of lymphoedema and distichiasis"]
article 157986141
Human Genetics
1980
pending pending 2026-04-21 07:03
none of these labels ["Zur Problematik des Polymorphismus des Bitterschmeckens: Vergleichende Untersuchungen an Thioharnstoffderivaten und Anetholtrithion"]
article 157992480
Human Genetics
1965
pending pending 2026-04-21 07:03
none of these labels ["CG dinucleotide transitions in the factor IX gene account for about half of the point mutations in hemophilia B patients: a Seattle series"]
article 158115024
Human Genetics
1991
pending pending 2026-04-21 07:03
none of these labels ["A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY"]
article 158120864
Human Genetics
1992
pending pending 2026-04-21 07:03
none of these labels ["Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss"]
article 158560591
Human Genetics
2004
pending pending 2026-04-21 07:03
none of these labels ["Mitochondrial DNA polymorphisms as risk factors for Parkinson?s disease and Parkinson?s disease dementia"]
article 159390102
Human Genetics
2004
pending pending 2026-04-21 07:03
none of these labels ["Decreased guanine nucleotide exchange factor activity in eIF2B-mutated patients"]
article 159887206
European Journal of Human Genetics
2004
pending pending 2026-04-21 07:03
none of these labels ["Genomewide Linkage Analysis for Internal Carotid Artery Intimal Medial Thickness: Evidence for Linkage to Chromosome 12"]
article 160383742
The American Journal of Human Genetics
2004
pending pending 2026-04-21 07:03
none of these labels ["Congenital deficiency of alpha‐fetoprotein and associated chromosomal abnormality in the placenta"]
article 162080042
American Journal of Medical Genetics Part A
2003
pending pending 2026-04-21 07:03
none of these labels ["Editorial Notes"]
article 163667182
Journal of Genetic Counseling
2003
pending pending 2026-04-21 07:03
none of these labels ["Kyphomelic dysplasia: a rare form of semilethal skeletal dysplasia"]
article 164025030
Clinical Genetics
2000
pending pending 2026-04-21 07:03
none of these labels ["The Biochemistry of Cell Signalling"]
article 164062585
Heredity
2001
pending pending 2026-04-21 07:03
none of these labels ["Closing Thoughts on Supervision"]
article 165148943
Journal of Genetic Counseling
2000
pending pending 2026-04-21 07:03
none of these labels ["Keyword Index, Volume 89"]
article 165353251
Heredity
2002
pending pending 2026-04-21 07:03
none of these labels ["Uniparental disomy of chromosome 2 resulting in lethal trifunctional protein deficiency due to homozygous ?-subunit mutations"]
article 165475070
Human Mutation
2002
pending pending 2026-04-21 07:03
none of these labels ["A PEX6-Defective Peroxisomal Biogenesis Disorder with Severe Phenotype in an Infant, versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents"]
article 166847665
The American Journal of Human Genetics
2002
pending pending 2026-04-21 07:03
none of these labels ["Mutations in a Novel Gene, TMIE, Are Associated with Hearing Loss Linked to the DFNB6 Locus"]
article 166984727
The American Journal of Human Genetics
2002
pending pending 2026-04-21 07:03
none of these labels ["The effect of reproductive compensation on recessive disorders within consanguineous human populations"]
article 167166854
Heredity
2002
pending pending 2026-04-21 07:03
none of these labels ["Removal of repetitive sequences from FISH probes using PCR-assisted affinity chromatography"]
article 167642881
Human Genetics
1997
pending pending 2026-04-21 07:03
none of these labels ["24 bp deletion and Ala1278 to val mutation of the ATP7B gene in a Sardinian family with Wilson disease"]
article 167670576
Human Mutation
1997
pending pending 2026-04-21 07:03
none of these labels ["Dual blastomere analysis improves reliability of preimplantation trembler mouse diagnosis"]
article 167842271
Human Genetics
1997
pending pending 2026-04-21 07:03
none of these labels ["DNA Pooling in Mutation Detection with Reference to Sequence Analysis"]
article 178617711
The American Journal of Human Genetics
2000
pending pending 2026-04-21 07:03
none of these labels ["Clinical characteristics and genotypes of 201 patients with mucopolysaccharidosis type <scp>II</scp> in China: A retrospective, observational study"]
article 179660410
Clinical Genetics
2023
pending pending 2026-04-21 07:03
none of these labels ["Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome"]
article 180837876
The American Journal of Human Genetics
2000
pending pending 2026-04-21 07:03
none of these labels ["Phenotypes of Patients with “Simple” Mendelian Disorders Are Complex Traits: Thresholds, Modifiers, and Systems Dynamics"]
article 185118234
The American Journal of Human Genetics
2000
pending pending 2026-04-21 07:03
none of these labels ["Further phenotypic delineation of Alazami syndrome"]
article 189303717
American Journal of Medical Genetics Part A
2022
pending pending 2026-04-21 07:03
none of these labels ["Expression of esterase D and other gene markers in trisomy 13"]
article 189509104
Human Genetics
1979
pending pending 2026-04-21 07:03
none of these labels ["A Locus for Autosomal Dominant Colobomatous Microphthalmia Maps to Chromosome 15q12-q15"]
article 191948050
The American Journal of Human Genetics
2000
pending pending 2026-04-21 07:03
none of these labels ["Prenatal detection of cystic fibrosis by ultrasonography: a retrospective study of more than 346 000 pregnancies"]
article 193733087
Journal of Medical Genetics
2002
pending pending 2026-04-21 07:03