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Peter Benn

24PUBLICATIONS
14CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Cell and nuclear divisionFoetal development and medicineObstetrics and gynaecologyReproductive medicine not elsewhere classified
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Publications (24)

Sort by Publication Date:
|Nov 27, 2025
Whole-genome paternal uniparental disomy identified through prenatal single-nucleotide polymorphism-based cell-free DNA screening.

P Benn, K Hashimoto, V Souter

|Sep 28, 2024
Chromosome segregation of human nonhomologous Robertsonian translocations: insights from preimplantation genetic testing.

Peter Benn, Katrina Merrion

|Jul 11, 2024
Accuracy of fetal fraction measurements in a single-nucleotide polymorphism-based noninvasive prenatal test.

Peter Benn, Jingwen Zhang, Daniel Lyons

|Mar 20, 2024
Reproductive Carrier Screening: Identifying Families at Risk for Familial Hypercholesterolemia in the United States.

Vivienne Souter, Emily Becraft, Samantha Brummitt

|Nov 22, 2023
Single gene non-invasive prenatal testing when the father is not available for testing; concerns regarding Wynn et al., Prenatal Diagnosis 2023. 43:1344-54.

John Williams, Peter Benn

|Nov 20, 2022
Positive predictive values and outcomes for uninformative cell-free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO study).

Francesca Romana Grati, Ilaria Bestetti, Daria De Siero

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Frequent Collaborators

4 joint publications

Francesca Romana Grati

3 joint publications

Zachary Demko

3 joint publications

Howard Cuckle

1 joint publications

A L Simon

1 joint publications

Sharon E Plon

1 joint publications

Diana W Bianchi

1 joint publications

Herman Hedriana

1 joint publications

Kimberly Martin

1 joint publications

Wendy DiNonno

1 joint publications

Yuval Yaron

Frequent Collaborators

4 joint publications

Francesca Romana Grati

3 joint publications

Zachary Demko

3 joint publications

Howard Cuckle

1 joint publications

A L Simon

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