Peter Benn
Overview
Explore the profile of Peter Benn including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
85
Citations
954
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
11.
12.
Demko Z, Prigmore B, Benn P
J Clin Med
. 2022 Aug;
11(16).
PMID: 36012999
Non-invasive prenatal testing (NIPT) for trisomies 21, 18, 13 and monosomy X is widely utilized with massively parallel shotgun sequencing (MPSS), digital analysis of selected regions (DANSR), and single nucleotide...
13.
Cuckle H, Benn P, Yaron Y
Prenat Diagn
. 2022 May;
42(8):959-961.
PMID: 35621153
No abstract available.
14.
Kantor V, Jelsema R, Xu W, DiNonno W, Young K, Demko Z, et al.
Prenat Diagn
. 2022 May;
42(8):994-999.
PMID: 35574995
Objective: An extra haplotype is infrequently encountered in single nucleotide polymorphism(SNP)-based non-invasive prenatal testing (NIPT) and is usually attributed to an undetected twin or triploidy. We reviewed a large series...
15.
Benn P, Rebarber A
Prenat Diagn
. 2021 Jun;
41(10):1233-1240.
PMID: 34170028
Twin pregnancies are common and associated with pregnancy complications and adverse outcomes. Prenatal clinical management is intensive and has been hampered by inferior screening and less acceptable invasive testing. For...
16.
Grati F, Malvestiti F, Gallazzi G, Saragozza S, Grimi B, Agrati C, et al.
Prenat Diagn
. 2021 Mar;
41(6):652-660.
PMID: 33782989
Objective: To provide an estimation of the probability of error when chorionic villi (CV) cytogenetic analysis is limited to a single placental layer; either a direct preparation (Dir) or long-term...
17.
Benn P, Cuckle H, Pergament E
Prenat Diagn
. 2021 Mar;
41(5):642-646.
PMID: 33720446
The presence of high levels of aneuploidy in oocytes and early embryos and their fate is of considerable scientific and clinical importance. The Origins of Aneuploidy Research Consortium (OARC) was...
18.
Benn P
Prenat Diagn
. 2020 Nov;
41(5):564-572.
PMID: 33179335
Uniparental disomy (UPD) is defined as two copies of a whole chromosome derived from the same parent. There can be multiple mechanisms that lead to UPD; these are reviewed in...
19.
Cuckle H, Benn P
Prenat Diagn
. 2020 Sep;
41(5):536-544.
PMID: 32895968
The birth prevalence of each common autosomal trisomy (21, 18 and 13) increases with advancing maternal age and this is the most important epidemiological risk factor. Prevalence during pregnancy is...
20.
Benn P, Grati F
Prenat Diagn
. 2020 Jul;
41(5):519-524.
PMID: 32677063
Objective: To review the mosaic autosomal trisomies in chorionic villi sample (CVS) trophoblasts, mesenchyme, and both cell lineages and to compare them with trisomies in spontaneous abortions. Methods: Mosaic autosomal...