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D. Pruss · SciRah

Researcher profile · Semantic Scholar

D. Pruss

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D. Pruss — researcher profile on SciRah

h-index: 21
Works: 48
Citations: 12K

Most-cited papers

A draft sequence of the rice genome (Oryza sativa L. ssp. japonica).
S. Goff, Darrell O. Ricke, Tien-Hung Lan, Gernot G. Presting +51 more
2002Science2,333 citations
Semantic Scholar
The genome of the domesticated apple (Malus × domestica Borkh.)
R. Velasco, A. Zharkikh, J. Affourtit, A. Dhingra +82 more
2010Nature Genetics2,000 citations
Semantic Scholar
A Draft Sequence of the Rice Genome (Oryza sativa L. ssp. japonica)
S. Goff, Darrell O. Ricke, Tien-Hung Lan, Gernot G. Presting +51 more
2002Science1,740 citations
Semantic Scholar
Whole-Genome Shotgun Assembly and Analysis of the Genome of Fugu rubripes
S. Aparício, J. Chapman, E. Stupka, N. Putnam +37 more
2002Science1,606 citations
Semantic Scholar
A High Quality Draft Consensus Sequence of the Genome of a Heterozygous Grapevine Variety
R. Velasco, A. Zharkikh, M. Troggio, Dustin A. Cartwright +53 more
2007PLoS ONE1,018 citations Open access
Semantic Scholar
Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals.
T. S. Frank, A. M. Deffenbaugh, J. Reid, M. Hulick +7 more
2002Journal of Clinical Oncology909 citations
Semantic Scholar
A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes.
D. Easton, A. M. Deffenbaugh, D. Pruss, Cynthia Frye +7 more
2007American Journal of Human Genetics437 citations Open access
Semantic Scholar
Somatic mutations in BRCA1 and BRCA2 could expand the number of patients that benefit from poly (ADP ribose) polymerase inhibitors in ovarian cancer.
B. Hennessy, K. Timms, M. Carey, A. Gutin +15 more
2010Journal of Clinical Oncology386 citations Open access
Semantic Scholar
BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast-ovarian cancer
M. Hall, J. Reid, L. A. Burbidge, D. Pruss +6 more
2009Cancer358 citations Open access
Semantic Scholar
A comprehensive laboratory‐based program for classification of variants of uncertain significance in hereditary cancer genes
J. Eggington, K. Bowles, K. Moyes, S. Manley +11 more
2014Clinical Genetics183 citations Open access
Semantic Scholar
Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance.
G. Chenevix-Trench, S. Healey, S. Lakhani, P. Waring +21 more
2006Cancer Research172 citations
Semantic Scholar
Functional assays for classification of BRCA2 variants of uncertain significance.
Daniel J. Farrugia, M. Agarwal, V. Pankratz, A. M. Deffenbaugh +8 more
2008Cancer Research116 citations Open access
Semantic Scholar
AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia
E. Virts, A. Jankowska, C. Mackay, M. Glaas +28 more
2015Human Molecular Genetics76 citations Open access
Semantic Scholar
Breast cancer brain metastases show increased levels of genomic aberration-based homologous recombination deficiency scores relative to their corresponding primary tumors
M. Dióssy, L. Reiniger, Z. Sztupinszki, M. Krzystanek +15 more
2018bioRxiv74 citations Open access
Semantic Scholar
Functional evaluation of BRCA2 variants mapping to the PALB2-binding and C-terminal DNA-binding domains using a mouse ES cell-based assay.
K. Biswas, R. Das, J. Eggington, Huan-Yu Qiao +14 more
2012Human Molecular Genetics63 citations Open access
Semantic Scholar
Impact of a Cancer Gene Variant Reclassification Program Over a 20-Year Period
L. Esterling, Ranjula Wijayatunge, K. Brown, B. Morris +5 more
2020JCO Precision Oncology44 citations Open access
Semantic Scholar
Development and validation of a new algorithm for the reclassification of genetic variants identified in the BRCA1 and BRCA2 genes
D. Pruss, B. Morris, E. Hughes, J. Eggington +8 more
2014Breast Cancer Research and Treatment42 citations
Semantic Scholar
Sequencing and assembly of highly heterozygous genome of Vitis vinifera L. cv Pinot Noir: problems and solutions.
A. Zharkikh, M. Troggio, D. Pruss, A. Cestaro +11 more
2008Journal of Biotechnology40 citations
Semantic Scholar
The BRCA2 genetic variant IVS7 + 2T → G is a mutation
M. Pyne, A. Brothman, B. Ward, D. Pruss +2 more
2000Journal of Human Genetics29 citations
Semantic Scholar
Exceptions to the rule: Case studies in the prediction of pathogenicity for genetic variants in hereditary cancer genes
E. Rosenthal, K. Bowles, D. Pruss, Aric van Kan +3 more
2015Clinical Genetics27 citations Open access
Semantic Scholar
Development and Validation of a Breast Cancer Polygenic Risk Score on the Basis of Genetic Ancestry Composition
E. Hughes, S. Wagner, D. Pruss, R. Bernhisel +25 more
2022JCO Precision Oncology23 citations Open access
Semantic Scholar
Targeting chromatin disruption: Transcription regulators that acetylate histones.
A. Wolffe, D. Pruss
1996Cell18 citations Open access
Semantic Scholar
Application of haplotype pair analysis for the identification of hemizygous loci
B. Hendrickson, D. Pruss, E. Lyon, T. Scholl
2003Journal of Medical Genetics9 citations Open access
Semantic Scholar
Biochemical and genetic characterisation shows that the BRCA1 IVS20 insertion is a polymorphism
T. Scholl, M. Pyne, Brian E. Ward, D. Pruss
1999Journal of Medical Genetics9 citations Open access
Semantic Scholar
Germline mutations in the â-catenin gene are not associated with the FAP phenotype without an APC mutation
M. Pyne, D. Pruss
8 citations
Semantic Scholar
Apple genome sequencing and post-genomic program at IASMA Research Center
R. Velasco, M. Troggio, A. Zharkikh, S. Salvi +36 more
20096 citations
Semantic Scholar
The molecular landscape of genome instability in prostate cancer (PC)
K. Timms, J. Cuzick, C. Neff, J. Reid +6 more
20165 citations Open access
Semantic Scholar
DNA-protein cross-linking applications for chromatin studies in vitro and in vivo.
D. Pruss, I. Gavin, S. Mel'nik, Sergei G. Bavykin
1999Methods in Enzymology5 citations
Semantic Scholar
Corrigendum to: Breast cancer brain metastases show increased levels of genomic aberration-based homologous recombination deficiency scores relative to their corresponding primary tumors
M. Dióssy, L. Reiniger, Z. Sztupinszki, M. Krzystanek +15 more
2019Annals of Oncology3 citations Open access
Semantic Scholar
Abstract P5-10-02: Development and validation of a polygenic score to predict breast cancer risk in unaffected Hispanic women negative for mutations on a multi-gene hereditary cancer panel
E. Hughes, S. Wagner, D. Pruss, SK Gallagher +8 more
2019Poster Session Abstracts3 citations
Semantic Scholar
The golden delicious apple genome sequencing project: progress and perspectives
R. Velasco, A. Zharkikh, M. Troggio, D. Pruss +24 more
20081 citations
Semantic Scholar
Targeting Chromatin Disruption : Minireview Transcription Regulators that Acetylate Histones
A. Wolffe, D. Pruss
19971 citations
Semantic Scholar
Abstract 3587: Independent validation of polygenic risk scores for overall and triple-negative breast cancer among high-risk African American women.
Yi-Jia Sun, Timothy Simmons, James Li, Armaan Jamal +7 more
2026Cancer Research0 citations
Semantic Scholar
Polygenic Risk Scores for Breast Cancer Among African American Women With High Risk
Yi-Jia Sun, Timothy Simmons, James Li, Armaan Jamal +7 more
2026JAMA Network Open0 citations Open access
Semantic Scholar
Interactions between polygenic variants and clinical factors as predictors of breast cancer risk in the UK Biobank.
Timothy Simmons, E. Hughes, S. Pruthi, Srikanth Jammulapati +8 more
2025Journal of Clinical Oncology0 citations
Semantic Scholar
O04: Longitudinal validation in UK Biobank of a breast cancer risk model combining a multiple-ancestry polygenic score with traditional risk factors
T. Simmons, E. Hughes, Srikanth Jammulapati, D. Pruss +9 more
2025Genetics in Medicine Open0 citations Open access
Semantic Scholar
2025 SMFM Oral Schedule
Seung-Mi Lee, H. Park, Soo-Ran Choi, Jeesun Lee +300 more
2025Pregnancy0 citations Open access
Semantic Scholar
Association of an ancestry-specific variant near the ESR1 gene with cancer risk and breast density in women of self-reported Hispanic ancestry.
E. Hughes, A. Kurian, Eudora Hu, M. Kucera +5 more
2025Journal of Clinical Oncology0 citations Open access
Semantic Scholar
Abstract PS16-01: Longitudinal validation in the UK Biobank of a breast cancer risk assessment tool that combines a polygenic score for all ancestries with traditional risk factors
Timothy Simmons, E. Hughes, Srikanth Jammulapati, D. Pruss +9 more
2025Clinical Cancer Research0 citations
Semantic Scholar
Abstract PS10-07: A second-generation polygenic risk score (PRS) based on genetic ancestry improves breast cancer (BC) risk prediction for all ancestries
Timothy Simmons, E. Hughes, D. Pruss, M. Kucera +10 more
2024Cancer Research0 citations
Semantic Scholar
Improving a polygenic risk score (PRS) for breast cancer (BC) risk assessment in diverse ancestries.
Timothy Simmons, E. Hughes, D. Pruss, M. Kucera +13 more
2024Journal of Clinical Oncology0 citations
Semantic Scholar
646P Prostate cancer metastatic profiles correlate with molecular alterations
O. Cussenot, E. Perrot, L. Brureau, P. Blanchet +6 more
20200 citations Open access
Semantic Scholar
Molecular phenotypes in DNA repair deficiency correlate with specific clinical outcomes subtypes and genetic background
O. Cussenot, E. Perrot, L. Brureau, P. Blanchet +6 more
2019European urology. Supplement0 citations
Semantic Scholar
Fugu rubripes Whole-Genome Shotgun Assembly and Analysis of the Genome of
S. Aparício, J. Chapman, E. Stupka, N. Putnam +37 more
20130 citations
Semantic Scholar
A dense SNP-based genetic linkage map of grapevine (Vitis Vinifera L.) anchored to the sequenced gen
R. Velasco, A. Zharkikh, M. Troggio, Satish K. Bhatnagar +20 more
20070 citations
Semantic Scholar
Vitis vinifera cv. Pinot noir: dealing with heterozygous genomes by merging sanger and pyrosequencing methods
R. Velasco, A. Zharkikh, M. Troggio, Satish K. Bhatnagar +20 more
20070 citations
Semantic Scholar
Deletions importantes dans le gene humain brca1 et utilisation correspondante
Thomas Scholl, Brant C. Hendrickson, Benjamin D. Ward, D. Pruss
20030 citations
Semantic Scholar
Methode d'egalisation d'intensites de bandes sur des gels de sequençage
Nadeem A. Tusneem, D. Pruss, M. Shen, Satish K. Bhatnagar
20010 citations
Semantic Scholar

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