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Author Details

Anna Newlin
NorthShore University HealthSystem
1990
22
14
PMIDPaper TitleJournal TitlePublished Year
35646064Utilizing Public Health Frameworks and Partnerships to Ensure Equity in DNA-Based Population Screening.Front Genet2022
35646064Utilizing Public Health Frameworks and Partnerships to Ensure Equity in DNA-Based Population Screening.Front Genet2022
29301143Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.Br J Cancer2018
32913991Postmortem Somatic Sequencing of Tumors From Patients With Suspected Lynch Syndrome Has Clinical Utility for Surviving Relatives.JCO Precis Oncol2018
29301143Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.Br J Cancer2018
29509747Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.Br J Cancer2018
32913991Postmortem Somatic Sequencing of Tumors From Patients With Suspected Lynch Syndrome Has Clinical Utility for Surviving Relatives.JCO Precis Oncol2018
29509747Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.Br J Cancer2018
26869169Evaluation of laboratory perspectives on hereditary cancer panels.Fam Cancer2016
26869169Evaluation of laboratory perspectives on hereditary cancer panels.Fam Cancer2016
27087319Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.Am J Hum Genet2016
27087319Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.Am J Hum Genet2016
25117502Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice.Fam Cancer2014
25117502Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice.Fam Cancer2014
2337786910 rare tumors that warrant a genetics referral.Fam Cancer2013
2337786910 rare tumors that warrant a genetics referral.Fam Cancer2013
22846732Genetic testing by cancer site: ovary.Cancer J2012
22846732Genetic testing by cancer site: ovary.Cancer J2012
20074521Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.Cell2010
20074521Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.Cell2010
18661230Psychological impact of recall in high-risk breast MRI screening.Breast Cancer Res Treat2009
18661230Psychological impact of recall in high-risk breast MRI screening.Breast Cancer Res Treat2009
17207529Genetic study of familial uveal melanoma: association of uveal and cutaneous melanoma with cutaneous and ocular nevi.Ophthalmology2007
17207529Genetic study of familial uveal melanoma: association of uveal and cutaneous melanoma with cutaneous and ocular nevi.Ophthalmology2007
16875934The I1307K APC polymorphism in Ashkenazi Jews with colorectal cancer: clinical and pathologic features.Cancer Genet Cytogenet2006
16875934The I1307K APC polymorphism in Ashkenazi Jews with colorectal cancer: clinical and pathologic features.Cancer Genet Cytogenet2006
14985297Characterization and prevalence of PITX2 microdeletions and mutations in Axenfeld-Rieger malformations.Invest Ophthalmol Vis Sci2004
14985297Characterization and prevalence of PITX2 microdeletions and mutations in Axenfeld-Rieger malformations.Invest Ophthalmol Vis Sci2004
14595441Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).Nat Genet2003
14595441Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).Nat Genet2003
11241501Trisomy 1q42qter "syndrome": additional case report.Am J Med Genet2001
11241501Trisomy 1q42qter "syndrome": additional case report.Am J Med Genet2001
10594873Mosaic trisomy 7 in a patient with pigmentary abnormalities.Am J Med Genet1999
10422858Discordance for keratoconus in two pairs of monozygotic twins.Cornea1999
10594873Mosaic trisomy 7 in a patient with pigmentary abnormalities.Am J Med Genet1999
10422858Discordance for keratoconus in two pairs of monozygotic twins.Cornea1999
8737648Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.Am J Med Genet1996
8737648Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.Am J Med Genet1996
8275571Prenatal detection of an inverted X chromosome in a male.Clin Genet1993
8275571Prenatal detection of an inverted X chromosome in a male.Clin Genet1993
1620349Causal heterogeneity in isolated lissencephaly.Neurology1992
1620349Causal heterogeneity in isolated lissencephaly.Neurology1992
2333913Evidence for a major gene in familial anencephaly.Am J Med Genet1990
2333913Evidence for a major gene in familial anencephaly.Am J Med Genet1990
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Collaborators

Scott M Weissman
Center for Medical Genetics, NorthShore University HealthSystem
Co-authored papers 5
Wendy S Rubinstein
CancerLinQ LLC, American Society of Clinical Oncology
Co-authored papers 3
William D Foulkes
Segal Cancer Centre, Jewish General Hospital
Co-authored papers 3
Susan M Domchek
Co-authored papers 2
Judy Kirk
Co-authored papers 2
Jan Lubinski
Pomeranian Medical University
Co-authored papers 2
Daniel Leongamornlert
Oncogenetics Team The Institute of Cancer Research London UK.
Co-authored papers 2
Nicholas Pachter
King Edward Memorial Hospital
Co-authored papers 2
Freddie C Hamdy
University of Oxford
Co-authored papers 2
Henrik Gr??nberg
Karolinska Institute
Co-authored papers 2
Christopher S Foster
The Institute of Cancer Research
Co-authored papers 2
Declan G Murphy
Peter MacCallum Cancer Centre, University of Melbourne
Co-authored papers 2
Tokhir Dadaev
The Institute of Cancer Research
Co-authored papers 2
Elizabeth Bancroft
The Institute of Cancer Research
Co-authored papers 2
Louise Izatt
Guy's and St Thomas' NHS Foundation Trust
Co-authored papers 2
Rosalind A Eeles
The Institute of Cancer Research
Co-authored papers 2
Christi J van Asperen
Leiden University Medical Center
Co-authored papers 2
Peter J Hulick
Neaman Center for Personalized Medicine, NorthShore University HealthSystem
Co-authored papers 2
Vincent Khoo
The Royal Marsden NHS Foundation Trust and Institute of Cancer Research
Co-authored papers 2
Zsofia Kote-Jarai
The Institute of Cancer Research
Co-authored papers 2
Cezary Cybulski
International Hereditary Cancer Center, Pomeranian Medical University
Co-authored papers 2
Lambertus A Kiemeney
Co-authored papers 2
Haran Sivakumaran
QIMR Berghofer Medical Research Institute
Co-authored papers 1
Sunil R Lakhani
University of Queensland
Co-authored papers 1
Theo Heller
National Institute of Diabetes and Digestive and Kidney Diseases
Co-authored papers 1
Alireza Heravi-Moussavi
Ferdowsi University of Mashhad
Co-authored papers 1
Pavel N Pichurin
Mayo Clinic
Co-authored papers 1
Nicola Waddell
QIMR Berghofer Medical Research Institute
Co-authored papers 1
Robert L Walker
Center for Cancer Research, National Cancer Institute, National Institutes of Health
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Release 1.2