Publications by authors named "Penelope Roberts"

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Biologically inspired robotic perception-action for soft fruit harvesting in vertical growing environments.
Fuli Wang, Rodolfo Cuan Urquizo, Penelope Roberts, Vishwanathan Mohan, Chris Newenham

Precis Agric· March 2023

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Utility of noninvasive genome-wide screening: a prospective cohort of obstetric patients undergoing diagnostic testing.
Stephanie Guseh, Louise Wilkins-Haug, Anjali Kaimal, Lisa Dunn-Albanese, Sophie Adams, Penelope Roberts

Genet Med· July 2021

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High Fetal Fraction on First Trimester Cell-Free DNA Aneuploidy Screening and Adverse Pregnancy Outcomes.
Lydia L Shook, Mark A Clapp, Penelope S Roberts, Sarah N Bernstein, Ilona T Goldfarb

Am J Perinatol· January 2020

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Low Fetal Fraction and Birth Weight in Women with Negative First-Trimester Cell-Free DNA Screening.
Mark A Clapp, Margaret Berry, Lydia L Shook, Penelope S Roberts, Ilona T Goldfarb

Am J Perinatol· January 2020

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Isolation of cancer stem like cells from human adenosquamous carcinoma of the lung supports a monoclonal origin from a multipotential tissue stem cell.
Jennie P Mather, Penelope E Roberts, Zhuangyu Pan, Francine Chen, Jeffrey Hooley

PLoS One· September 2014

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Establishment of human ovarian serous carcinomas cell lines in serum free media.
Zhuangyu Pan, Jeffrey Hooley, Douglas H Smith, Peter Young, Penelope E Roberts

Methods· March 2012

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Identification of a novel kindred with familial pancreatitis and pancreatic cancer.
Jennifer LaFemina, Penelope A Roberts, Yin P Hung, James F Gusella, Dushyant Sahani

Pancreatology· September 2009

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Isolation and establishment of human tumor stem cells.
Penelope E Roberts

Methods Cell Biol· July 2008

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Identification of 54 large deletions/duplications in TSC1 and TSC2 using MLPA, and genotype-phenotype correlations.
Piotr Kozlowski, Penelope Roberts, Sandra Dabora, David Franz, John Bissler

Hum Genet· May 2007

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Unusually mild tuberous sclerosis phenotype is associated with TSC2 R905Q mutation.
An C Jansen, Ozgur Sancak, Maria Daniela D'Agostino, Amanpreet Badhwar, Penelope Roberts

Ann Neurol· November 2006

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Clinical and genotype studies of cardiac tumors in 154 patients with tuberous sclerosis complex.
Sergiusz Jóźwiak, Katarzyna Kotulska, Jolanta Kasprzyk-Obara, Dorota Domańska-Pakieła, Małgorzata Tomyn-Drabik, Penelope Roberts

Pediatrics· October 2006

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Pathogenesis of tuberous sclerosis subependymal giant cell astrocytomas: biallelic inactivation of TSC1 or TSC2 leads to mTOR activation.
Jennifer A Chan, Hongbing Zhang, Penelope S Roberts, Sergiusz Jozwiak, Grajkowska Wieslawa

J Neuropathol Exp Neurol· December 2004

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A 34 bp deletion within TSC2 is a rare polymorphism, not a pathogenic mutation.
Penelope S Roberts, Vijaya Ramesh, Sandra Dabora, David J Kwiatkowski

Ann Hum Genet· November 2003

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Association between a high-expressing interferon-gamma allele and a lower frequency of kidney angiomyolipomas in TSC2 patients.
Sandra L Dabora, Penelope Roberts, Andres Nieto, Ron Perez, Sergiusz Jozwiak

Am J Hum Genet· October 2002

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SNP identification, haplotype analysis, and parental origin of mutations in TSC2.
Penelope S Roberts, Joon Chung, Sergiusz Jozwiak, Sandra L Dabora, David N Franz

Hum Genet· July 2002

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