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Author Details

Zalman Vaksman
Children's Hospital of Philadelphia
2007
38
15
PMIDPaper TitleJournal TitlePublished Year
37688570BARD1 germline variants induce haploinsufficiency and DNA repair defects in neuroblastoma.J Natl Cancer Inst2024
37688579Germline pathogenic variants in neuroblastoma patients are enriched in BARD1 and predict worse survival.J Natl Cancer Inst2024
37688570BARD1 germline variants induce haploinsufficiency and DNA repair defects in neuroblastoma.J Natl Cancer Inst2024
37688579Germline pathogenic variants in neuroblastoma patients are enriched in BARD1 and predict worse survival.J Natl Cancer Inst2024
36541551Alternative lengthening of telomeres (ALT) in pediatric high-grade gliomas can occur without ATRX mutation and is enriched in patients with pathogenic germline mismatch repair (MMR) variants.Neuro Oncol2023
38076939AutoGVP: a dockerized workflow integrating ClinVar and InterVar germline sequence variant classification.bioRxiv2023
36778420<i>BARD1</i> germline variants induce haploinsufficiency and DNA repair defects in neuroblastoma.bioRxiv2023
36747619Germline pathogenic variants in 786 neuroblastoma patients.medRxiv2023
36541551Alternative lengthening of telomeres (ALT) in pediatric high-grade gliomas can occur without ATRX mutation and is enriched in patients with pathogenic germline mismatch repair (MMR) variants.Neuro Oncol2023
37492101OpenPBTA: The Open Pediatric Brain Tumor Atlas.Cell Genom2023
38076939AutoGVP: a dockerized workflow integrating ClinVar and InterVar germline sequence variant classification.bioRxiv2023
37492101OpenPBTA: The Open Pediatric Brain Tumor Atlas.Cell Genom2023
36747619Germline pathogenic variants in 786 neuroblastoma patients.medRxiv2023
36778420<i>BARD1</i> germline variants induce haploinsufficiency and DNA repair defects in neuroblastoma.bioRxiv2023
35131881Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility.Cancer Epidemiol Biomarkers Prev2022
35131881Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility.Cancer Epidemiol Biomarkers Prev2022
33918978A G316A Polymorphism in the Ornithine Decarboxylase Gene Promoter Modulates MYCN-Driven Childhood Neuroblastoma.Cancers (Basel)2021
33918978A G316A Polymorphism in the Ornithine Decarboxylase Gene Promoter Modulates MYCN-Driven Childhood Neuroblastoma.Cancers (Basel)2021
31605138Neural crest-derived tumor neuroblastoma and melanoma share 1p13.2 as susceptibility locus that shows a long-range interaction with the SLC16A1 gene.Carcinogenesis2020
31613963Pediatric high-grade glioma resources from the Children's Brain Tumor Tissue Consortium.Neuro Oncol2020
32096864Mitochondrial DNA Haplogroups and Susceptibility to Neuroblastoma.J Natl Cancer Inst2020
31605138Neural crest-derived tumor neuroblastoma and melanoma share 1p13.2 as susceptibility locus that shows a long-range interaction with the SLC16A1 gene.Carcinogenesis2020
32796005Somatic structural variation targets neurodevelopmental genes and identifies <i>SHANK2</i> as a tumor suppressor in neuroblastoma.Genome Res2020
33115534Genetic predisposition to longer telomere length and risk of childhood, adolescent and adult-onset ependymoma.Acta Neuropathol Commun2020
32607579European genetic ancestry associated with risk of childhood ependymoma.Neuro Oncol2020
32096864Mitochondrial DNA Haplogroups and Susceptibility to Neuroblastoma.J Natl Cancer Inst2020
33115534Genetic predisposition to longer telomere length and risk of childhood, adolescent and adult-onset ependymoma.Acta Neuropathol Commun2020
32607579European genetic ancestry associated with risk of childhood ependymoma.Neuro Oncol2020
32796005Somatic structural variation targets neurodevelopmental genes and identifies <i>SHANK2</i> as a tumor suppressor in neuroblastoma.Genome Res2020
31613963Pediatric high-grade glioma resources from the Children's Brain Tumor Tissue Consortium.Neuro Oncol2020
30793172Differences in Genomic Profiles and Outcomes Between Thoracic and Adrenal Neuroblastoma.J Natl Cancer Inst2019
31693904Genomic Profiling of Childhood Tumor Patient-Derived Xenograft Models to Enable Rational Clinical Trial Design.Cell Rep2019
31279991Neuroblastoma in relation to joint effects of vitamin A and maternal and offspring variants in vitamin A-related genes: A report of the Children's Oncology Group.Cancer Epidemiol2019
31474320Germline 16p11.2 Microdeletion Predisposes to Neuroblastoma.Am J Hum Genet2019
30793172Differences in Genomic Profiles and Outcomes Between Thoracic and Adrenal Neuroblastoma.J Natl Cancer Inst2019
31693904Genomic Profiling of Childhood Tumor Patient-Derived Xenograft Models to Enable Rational Clinical Trial Design.Cell Rep2019
31474320Germline 16p11.2 Microdeletion Predisposes to Neuroblastoma.Am J Hum Genet2019
31279991Neuroblastoma in relation to joint effects of vitamin A and maternal and offspring variants in vitamin A-related genes: A report of the Children's Oncology Group.Cancer Epidemiol2019
30132831Fine mapping of 2q35 high-risk neuroblastoma locus reveals independent functional risk variants and suggests full-length BARD1 as tumor-suppressor.Int J Cancer2018
30132831Fine mapping of 2q35 high-risk neuroblastoma locus reveals independent functional risk variants and suggests full-length BARD1 as tumor-suppressor.Int J Cancer2018
28033528Neuroblastoma survivors are at increased risk for second malignancies: A report from the International Neuroblastoma Risk Group Project.Eur J Cancer2017
28545128Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma.PLoS Genet2017
28924153Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.Nat Commun2017
29117357Evaluation of Genetic Predisposition for MYCN-Amplified Neuroblastoma.J Natl Cancer Inst2017
28033528Neuroblastoma survivors are at increased risk for second malignancies: A report from the International Neuroblastoma Risk Group Project.Eur J Cancer2017
29117357Evaluation of Genetic Predisposition for MYCN-Amplified Neuroblastoma.J Natl Cancer Inst2017
28924153Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.Nat Commun2017
28545128Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma.PLoS Genet2017
27278669Genomic leftovers: identifying novel microsatellites, over-represented motifs and functional elements in the human genome.Sci Rep2016
27278669Genomic leftovers: identifying novel microsatellites, over-represented motifs and functional elements in the human genome.Sci Rep2016
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Collaborators

Sharon J Diskin
Children's Hospital of Philadelphia
Co-authored papers 25
John M Maris
Children's Hospital of Philadelphia
Co-authored papers 15
Hakon Hakonarson
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 10
Gonzalo L??pez
Children's Hospital of Philadelphia
Co-authored papers 7
Jung Kim
Clinical Genetics Branch, National Cancer Institute
Co-authored papers 5
Kristina A Cole
Perelman School of Medicine, University of Pennsylvania
Co-authored papers 5
Adam C Resnick
Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
Co-authored papers 4
Kristopher R Bosse
Co-authored papers 4
Komal S Rathi
Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
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Douglas R Stewart
Clinical Genetics Branch, National Cancer Institute
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Krutika S Gaonkar
Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
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Andrew F Olshan
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Jan Koster
Amsterdam University Medical Centers location AMC
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Phillip B Storm
Children's Hospital of Philadelphia
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Pichai Raman
Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
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Mariarita Santi
Children's Hospital of Philadelphia
Co-authored papers 3
Javed Khan
Center for Cancer Research, National Cancer Institute
Co-authored papers 3
Jun S Wei
Center for Cancer Research, National Cancer Institute
Co-authored papers 3
Angela J Waanders
Ann & Robert H. Lurie Children's Hospital
Co-authored papers 3
Apexa Modi
Abbvie Inc., Genomics Research Center
Co-authored papers 3
Yiran Guo
Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
Co-authored papers 3
Daniela S Gerhard
National Cancer Institute
Co-authored papers 3
Jaime M Guidry Auvil
National Cancer Institute
Co-authored papers 3
Maura Diamond
Co-authored papers 3
Gregory P Way
Broad Institute of MIT and Harvard
Co-authored papers 2
Rishi R Lulla
Hasbro Children's Hospital, Brown University.
Co-authored papers 2
Mateusz Koptyra
Children's Hospital of Philadelphia
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Yael P Mosse
Perelman School of Medicine at the University of Pennsylvania
Co-authored papers 2
Cassie Kline
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Release 1.2