Author details

Full Name

Kristin Zelley

Affiliation

ORCID

Career Start Year

2012

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37428016	Rates of Intervention and Cancer Detection on Initial versus Subsequent Whole-body MRI Screening in Li-Fraumeni Syndrome.		2023
35232817	A novel <i>TP53</i> tandem duplication in a child with Li-Fraumeni syndrome.	Cold Spring Harb Mol Case Stud	2022
35923098	Looking closely at overgrowth: Constitutional mosaicism in PTEN hamartoma tumor syndrome.	Clin Genet	2022
35278038	Neuroblastoma and cutaneous angiosarcoma in a child with PTEN hamartoma tumor syndrome.	Pediatr Blood Cancer	2022
33097490	Phenotypic Differences in Juvenile Polyposis Syndrome With or Without a Disease-causing <i>SMAD4</i>/<i>BMPR1A</i> Variant.	Cancer Prev Res (Phila)	2021
32554798	A germline <i>PALB2</i> pathogenic variant identified in a pediatric high-grade glioma.	Cold Spring Harb Mol Case Stud	2020
32246378	Frequency of radiation-induced malignancies post-adjuvant radiotherapy for breast cancer in patients with Li-Fraumeni syndrome.	Breast Cancer Res Treat	2020
33887726	The Clinical Spectrum of PTEN Hamartoma Tumor Syndrome: Exploring the Value of Thyroid Surveillance.	Horm Res Paediatr	2020
32817165	A pedigree-based prediction model identifies carriers of deleterious de novo mutations in families with Li-Fraumeni syndrome.	Genome Res	2020
32675277	A Rare <i>TP53</i> Mutation Predominant in Ashkenazi Jews Confers Risk of Multiple Cancers.	Cancer Res	2020
31211762	Gastrointestinal Polyposis in Pediatric Patients.	Journal of Pediatric Gastroenterology and Nutrition	2019
32783018	Pediatric Somatic Tumor Sequencing Identifies Underlying Cancer Predisposition.	JCO Precis Oncol	2019
30243621	Earlier Colorectal Cancer Screening May Be Necessary In Patients With Li-Fraumeni Syndrome.	Gastroenterology	2019
29204812	Tumor Screening in Beckwith-Wiedemann Syndrome: Parental Perspectives.	Journal of Genetic Counseling	2018
30009566	Parent-child communication surrounding genetic testing for Li-Fraumeni syndrome: Living under the cloud of cancer.	Pediatr Blood Cancer	2018
29909594	The Influence of Adolescence on Parents' Perspectives of Testing and Discussing Inherited Cancer Predisposition.	J Genet Couns	2018
28303452	Should Genetic Testing be Offered for Children? The Perspectives of Adolescents and Emerging Adults in Families with Li-Fraumeni Syndrome.	J Genet Couns	2017
28674121	Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.	Clin Cancer Res	2017
28674120	Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma.	Clin Cancer Res	2017
28674117	Genetic Counselor Recommendations for Cancer Predisposition Evaluation and Surveillance in the Pediatric Oncology Patient.	Clin Cancer Res	2017
28620009	Recommendations for Cancer Surveillance in Individuals with RASopathies and Other Rare Genetic Conditions with Increased Cancer Risk.	Clin Cancer Res	2017
28066990	Management of adrenal masses in patients with Beckwith-Wiedemann syndrome.	Pediatr Blood Cancer	2017
25223899	Parent decision-making around the genetic testing of children for germline TP53 mutations.	Cancer	2015
25706929	Diagnosis of 9q22.3 microdeletion syndrome in utero following identification of craniosynostosis, overgrowth, and skeletal anomalies.	Am J Med Genet A	2015
26204294	Diagnostic Performance of Whole-Body MRI as a Tool for Cancer Screening in Children With Genetic Cancer-Predisposing Conditions.	AJR Am J Roentgenol	2015
24857136	Predisposition to pediatric and hematologic cancers: a moving target.	Am Soc Clin Oncol Educ Book	2014
23692048	Treatment of Epstein Barr virus-induced haemophagocytic lymphohistiocytosis with rituximab-containing chemo-immunotherapeutic regimens.	Br J Haematol	2013
23532898	Bilateral pheochromocytomas, hemihyperplasia, and subtle somatic mosaicism: the importance of detecting low-level uniparental disomy.	Am J Med Genet A	2013
23804593	Clinical features of three girls with mosaic genome-wide paternal uniparental isodisomy.	Am J Med Genet A	2013
24451799	Identification, management, and evaluation of children with cancer-predisposition syndromes.	Am Soc Clin Oncol Educ Book	2012