Douglas R. Stewart

Also affiliated with Cancer Genetics (United States), Division of Cancer Epidemiology and Genetics

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 2%percentile

3.3Author DataRank

Indexed papers

8in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 8 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Pathogenic Germline Variants in Cancer Susceptibility Genes in Children and Young Adults With Rhabdomyosarcoma

JCO Precision Oncology(2021)10.1200/po.20.00218

Top 16%

1.3DataRank

Top 16%45 citations

Nicholas Light, Vallijah Subasri, Erin L. Young, Talía Wegman-Ostrosky, Donald A. Barkauskas +21 more

Papers

Driven by 78 papers — median percentile 36. Top paper: “ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)”.

ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2021)10.1038/s41436-021-01172-3

N/A

13.5DataRank · unranked

563 citations

Kristy Lee, Wendy K. Chung, Allan Gordon, Gail E. Herman, Teri E. Klein +13 more

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2021)10.1038/s41436-021-01171-4

N/A

9.7DataRank · unranked

266 citations

Kristy Lee, Allan Gordon, Laura M. Amendola, Kathy Adelman, Sherri J. Bale +13 more

Genomic and evolutionary classification of lung cancer in never smokers

Nature Genetics(2021)10.1038/s41588-021-00920-0

N/A

5.4DataRank · unranked

248 citations

Philippe Joubert, Naser Ansari‐Pour, Zhao Wei, Phuc H. Hoang, Rachel Lokanga +56 more

Variable population prevalence estimates of germline TP53 variants: A gnomAD-based analysis

Human Mutation(2018)10.1002/humu.23673

N/A

4.7DataRank · unranked

96 citations

Megan N. Frone, Payal P. Khincha, Jung Kim, Amina Amadou, Fernanda P. Fortes +12 more

Correction to: ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2021)10.1038/s41436-021-01278-8

N/A

1.6DataRank · unranked

29 citations

Kristy Lee, Wendy K. Chung, Allan Gordon, Gail E. Herman, Teri E. Klein +13 more

Germline pathogenic variants in neuroblastoma patients are enriched in BARD1 and predict worse survival

JNCI Journal of the National Cancer Institute(2023)10.1093/jnci/djad183

N/A

1.3DataRank · unranked

27 citations

Zalman Vaksman, Laura E. Egolf, Rebecca S. Kaufman, Perry Evans, Karina L. Conkrite +23 more

Pathogenic Germline Variants in Cancer Susceptibility Genes in Children and Young Adults With Rhabdomyosarcoma

JCO Precision Oncology(2021)10.1200/po.20.00218

Top 16%

1.3DataRank

Top 16%45 citations

Nicholas Light, Vallijah Subasri, Erin L. Young, Talía Wegman-Ostrosky, Donald A. Barkauskas +21 more

OpenPBTA: The Open Pediatric Brain Tumor Atlas

Cell Genomics(2023)10.1016/j.xgen.2023.100340

Top 16%

1.3DataRank

Top 16%62 citations

Krutika S. Gaonkar, Stephanie J. Spielman, Candace L. Savonen, Chanté J. Bethell, Run Jin +61 more

Update on Cancer Predisposition Syndromes and Surveillance Guidelines for Childhood Brain Tumors

Clinical Cancer Research(2024)10.1158/1078-0432.ccr-23-4033

N/A

0.929DataRank · unranked

47 citations

Anirban Das, Rose B. McGee, Yoshiko Nakano, Jack Brzezinski, Sarah Scollon +14 more

ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2023)10.1016/j.gim.2023.100866

N/A

0.911DataRank · unranked

433 citations

Kristy Lee, Noura S. Abul‐Husn, Laura M. Amendola, Kyle B. Brothers, Wendy K. Chung +9 more

Specifications of the ACMG/AMP Variant Classification Guidelines for Germline DICER1 Variant Curation

Human Mutation(2023)10.1155/2023/9537832

N/A

0.746DataRank · unranked

15 citations

Megan N. Frone, Hannah C. Cox, Stephanie B. Crowley, Susan Hiraki, Noriko N. Yokoyama +20 more

Germline Cancer Predisposition Variants in Pediatric Rhabdomyosarcoma: A Report From the Children’s Oncology Group

JNCI Journal of the National Cancer Institute(2020)10.1093/jnci/djaa204

N/A

0.705DataRank · unranked

109 citations

Saumya D. Sisoudiya, Bailey A. Martin‐Giacalone, Michael M. Khayat, Shannon Dugan‐Perez, Deborah A. Marquez-Do +16 more

Advancing RAS/RASopathy therapies: An NCI‐sponsored intramural and extramural collaboration for the study of RASopathies

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61485

N/A

0.624DataRank · unranked

63 citations

Megan N. Frone, Karen W. Gripp, Bruce D. Gelb, Lisa Schoyer, Lisa Schill +17 more

Germline Exome Sequencing for Men with Testicular Germ Cell Tumor Reveals Coding Defects in Chromosomal Segregation and Protein-targeting Genes

European Urology(2023)10.1016/j.eururo.2023.05.008

N/A

0.579DataRank · unranked

19 citations

Jung Kim, Jonathan P. Bradfield, Scott M. Damrauer, Kurt D’Andrea, Lawrence H. Einhorn +14 more

A Genome-First Approach to Characterize DICER1 Pathogenic Variant Prevalence, Penetrance, and Phenotype

JAMA Network Open(2021)10.1001/jamanetworkopen.2021.0112

N/A

0.578DataRank · unranked

46 citations

Jung Kim, Ana F. Best, Zongming E. Chen, Ying Hu, Jeremy S. Haley +15 more

A genotype-first approach to exploring Mendelian cardiovascular traits with clear external manifestations

Genetics in Medicine(2020)10.1038/s41436-020-00973-2

N/A

0.564DataRank · unranked

42 citations

Nihir Patel, Madeline Lui, Arden Moscati, Ron Do, Douglas R. Stewart +6 more

DICER1 RNase IIIb domain mutations trigger widespread miRNA dysregulation and MAPK activation in pediatric thyroid cancer

Frontiers in Endocrinology(2023)10.3389/fendo.2023.1083382

N/A

0.561DataRank · unranked

41 citations

Victoria Casado‐Medrano, Erin R. Reichenberger, Zachary Spangler, Michele Scheerer, Amber Isaza +10 more

Incidence of Benign Meningiomas in the United States: Current and Future Trends

JNCI Cancer Spectrum(2021)10.1093/jncics/pkab035

N/A

0.529DataRank · unranked

33 citations

Douglas R. Stewart, Victoria Kennerley, Valentina I. Petkov, Philip S. Rosenberg, Ana F. Best +1 more

Comparative clinical and genomic analysis of neurofibromatosis type 2-associated cranial and spinal meningiomas

Scientific Reports(2020)10.1038/s41598-020-69074-z

N/A

0.524DataRank · unranked

32 citations

Ramita Dewan, Nancy F. Hansen, Settara C. Chandrasekharappa, Abhik Ray‐Chaudhury, Kristine Jones +7 more

Update on Pediatric Cancer Surveillance Recommendations for Patients with Neurofibromatosis Type 1, Noonan Syndrome, CBL Syndrome, Costello Syndrome, and Related RASopathies

Clinical Cancer Research(2024)10.1158/1078-0432.ccr-24-1611

N/A

0.524DataRank · unranked

32 citations

Anirban Das, Sarah Scollon, Sarah G. Mitchell, Mary‐Louise C. Greer, Marielle E. Yohe +22 more

Update on Pediatric Surveillance Recommendations for PTEN Hamartoma Tumor Syndrome, DICER1- Related Tumor Predisposition, and Tuberous Sclerosis Complex

Clinical Cancer Research(2024)10.1158/1078-0432.ccr-24-1947

N/A

0.515DataRank · unranked

30 citations

Suzanne P. MacFarland, Melissa R. Perrino, Sarah G. Mitchell, Junne Kamihara, Alexander T. Nelson +18 more

Increase in power by obtaining 10 or more controls per case when type-1 error is small in large-scale association studies

BMC Medical Research Methodology(2023)10.1186/s12874-023-01973-x

N/A

0.505DataRank · unranked

28 citations

Sonja I. Berndt, Mitchell J. Machiela, Douglas R. Stewart, Montserrat García‐Closas, Jung Kim +4 more

A Genome-First Approach to Estimate Prevalence of Germline Pathogenic Variants and Risk of Pancreatic Cancer in Select Cancer Susceptibility Genes

Cancers(2022)10.3390/cancers14133257

N/A

0.483DataRank · unranked

24 citations

Jung Kim, Jeremy S. Haley, Sun Young Kim, H. Shanker Rao, David J. Carey +3 more

Adult-Onset Cancer Predisposition Syndromes in Children and Adolescents—To Test or not to Test?

Clinical Cancer Research(2024)10.1158/1078-0432.ccr-23-3683

N/A

0.477DataRank · unranked

23 citations

Philip J. Lupo, Kristin Zelley, Jaclyn Schienda, Kim E. Nichols, Douglas R. Stewart +6 more

In search of genetic factors predisposing to familial hairy cell leukemia (HCL): exome-sequencing of four multiplex HCL pedigrees

Leukemia(2020)10.1038/s41375-019-0702-7

N/A

0.464DataRank · unranked

7 citations

Anand Pathak, Samantha Jones, Ramita Dewan, Jessica Merberg, Sirisha Karra +17 more

Alternative 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-Oncology(2022)10.1093/neuonc/noac278

N/A

0.457DataRank · unranked

20 citations

Heba Ijaz, Krutika S. Gaonkar, Rebecca S. Kaufman, Run Jin, Anastasios Karras +18 more

Gynecologic and reproductive health in patients with pathogenic germline variants in DICER1

Gynecologic Oncology(2020)10.1016/j.ygyno.2019.12.037

N/A

0.449DataRank · unranked

19 citations

Laura A. Harney, Nina Vyas, Averyl Bachi, Ann G. Carr, D. Ashley Hill +5 more

Genome-first approach of the prevalence and cancer phenotypes of pathogenic or likely pathogenic germline TP53 variants

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100242

N/A

0.449DataRank · unranked

19 citations

Natasha T. Strande, Jung Kim, Jeremy S. Haley, Jessica N. Hatton, Megan N. Frone +13 more

Testicular Sertoli cell tumour and potentially testicular Leydig cell tumour are features of DICER1 syndrome

Journal of Medical Genetics(2021)10.1136/jmedgenet-2020-107434

N/A

0.406DataRank · unranked

14 citations

Lauren M. Vasta, Valérie Duflos, Carole Corsini, Catherine Dubois d’Enghien, Mary L. McMaster +17 more

AutoGVP: a dockerized workflow integrating ClinVar and InterVar germline sequence variant classification

Bioinformatics(2024)10.1093/bioinformatics/btae114

N/A

0.406DataRank · unranked

14 citations

Ammar S. Naqvi, Ryan J Corbett, Rebecca S. Kaufman, Zalman Vaksman, Miguel A. Brown +9 more

Update on Cancer and Central Nervous System Tumor Surveillance in Pediatric NF2 -, SMARCB1 -, and LZTR1 -Related Schwannomatosis

Clinical Cancer Research(2025)10.1158/1078-0432.ccr-24-3278

N/A

0.373DataRank · unranked

11 citations

Marjolijn C.J. Jongmans, Gail E. Tomlinson, Mary‐Louise C. Greer, Sarah Scollon, Sarah G. Mitchell +18 more

Unusual phenotypes in patients with a pathogenic germline variant in DICER1

Familial Cancer(2021)10.1007/s10689-021-00271-z

N/A

0.373DataRank · unranked

11 citations

Miriam Elbracht, Julia Carlens, Peter Deutz, Felix Zeppernick, Lisa Lassay +10 more

OpenPBTA: An Open Pediatric Brain Tumor Atlas

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.13.507832

Top 49%

0.363DataRank

Top 49%7 citations

Krutika S. Gaonkar, Candace L. Savonen, Stephanie J. Spielman, Chanté J. Bethell, Run Jin +59 more

Update on Cancer Screening in Children with Syndromes of Bone Lesions, Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome, and Other Rare Syndromes

Clinical Cancer Research(2024)10.1158/1078-0432.ccr-24-2171

N/A

0.360DataRank · unranked

10 citations

Sun Young Kim, Sarah G. Mitchell, Marjolijn C.J. Jongmans, Jonathan D. Wasserman, Melissa R. Perrino +14 more

A genome-first approach to characterize DICER1 pathogenic variant prevalence, penetrance and cancer, thyroid, and other phenotypes in 2 population-scale cohorts

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101846

Top 50%

0.355DataRank

Top 50%9 citations

Jeremy S. Haley, Jessica N. Hatton, Uyenlinh L Mirshahi, H. Shanker Rao, Mark Ramos +6 more

Inflated expectations: Rare-variant association analysis using public controls

PLoS ONE(2023)10.1371/journal.pone.0280951

N/A

0.345DataRank · unranked

9 citations

Danielle M. Karyadi, Stephen W. Hartley, Bin Zhu, Mingyi Wang, Dongjing Wu +15 more

Endemic Burkitt Lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility

Leukemia(2020)10.1038/s41375-020-01052-w

N/A

0.312DataRank · unranked

7 citations

Isaac Otim, Martin D. Ogwang, Mingyi Wang, Bin Zhu, Nathan Cole +31 more

Genome-first determination of the prevalence and penetrance of eight germline myeloid malignancy predisposition genes: a study of two population-based cohorts

Leukemia(2024)10.1038/s41375-024-02436-y

N/A

0.312DataRank · unranked

7 citations

Jung Kim, Jeremy S. Haley, Mark Ramos, Uyenlinh L Mirshahi, David J. Carey +3 more

The landscape of rare genetic variants in familial Waldenström macroglobulinemia

Blood Neoplasia(2024)10.1016/j.bneo.2024.100013

N/A

0.294DataRank · unranked

3 citations

Jung Kim, Wen Luo, Jia Liu, C. Edmund Graham, Kristine Jones +7 more

Germline pathogenic variants in 786 neuroblastoma patients

medRxiv(2023)10.1101/2023.01.23.23284864

N/A

0.292DataRank · unranked

6 citations

Zalman Vaksman, Laura E. Egolf, Rebecca S. Kaufman, Perry Evans, Karina L. Conkrite +23 more

Most Fanconi anemia heterozygotes are not at increased cancer risk: A genome-first DiscovEHR cohort population study

Genetics in Medicine(2023)10.1016/j.gim.2023.101042

N/A

0.292DataRank · unranked

6 citations

Burak Altintas, Jeremy S. Haley, Jung Kim, Mark Ramos, David J. Carey +3 more

Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition

Clinical Cancer Research(2025)10.1158/1078-0432.ccr-24-2785

N/A

0.292DataRank · unranked

6 citations

Lisa Golmard, Jung Kim, Riyue Bao, Frank Y. Lin, Angshumoy Roy +32 more

Genomic ascertainment for UBA1 variants and VEXAS syndrome: a population-based study

medRxiv(2022)10.1101/2022.07.27.22277962

N/A

0.241DataRank · unranked

4 citations

Dale L. Bodian, Vandan Shah, Uyenlinh L Mirshahi, Jung Kim, Yi Ding +11 more

Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family

Familial Cancer(2021)10.1007/s10689-021-00267-9

N/A

0.241DataRank · unranked

4 citations

Mai Xu, Michael R. Sargen, Hyunbum Jang, Mingzhen Zhang, Tongwu Zhang +24 more

AutoGVP: a dockerized workflow integrating ClinVar and InterVar germline sequence variant classification

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.29.569103

N/A

0.208DataRank · unranked

3 citations

Ammar S. Naqvi, Ryan J. Corbett, Rebecca S. Kaufman, Zalman Vaksman, Miguel A. Brown +9 more

Genomic ascertainment of CHEK2 -related cancer predisposition

medRxiv(2024)10.1101/2024.08.07.24311613

N/A

0.179DataRank · unranked

1 citations

Jung Kim, Mark Ramos, Jeremy S. Haley, Diane T. Smelser, H. Shanker Rao +6 more

Lack of pathogenic germline DICER1 variants in males with testicular germ-cell tumors

Cancer Genetics(2020)10.1016/j.cancergen.2020.10.002

N/A

0.165DataRank · unranked

2 citations

Mary L. McMaster, Laura A. Harney, Alexander Ling, Jung Kim, Anne K. Harris +11 more

Increased frequency of CHEK2 germline pathogenic variants among individuals with dermatofibrosarcoma protuberans

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101895

N/A

0.165DataRank · unranked

2 citations

Jung Kim, Jeremy S. Haley, Hayley P Barker, Piyushkumar A. Mundra, Mandy L. Ballinger +5 more

Data underlying OpenPBTA Manuscript Figures and Molecular Alterations

Zenodo (CERN European Organization for Nuclear Research)(2023)10.5281/zenodo.7805407

Top 78%

0.104DataRank

Top 78%1 citations

Krutika S. Gaonkar, Stephanie J. Spielman, Candace L. Savonen, Chanté J. Bethell, Run Jin +63 more

Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family

medRxiv(2021)10.1101/2021.04.20.21254596

N/A

0.104DataRank · unranked

1 citations

Mai Xu, Michael R. Sargen, Hyunbum Jang, Mingzhen Zhang, Tongwu Zhang +24 more

TERT c.3150 G > C (p.K1050N): a founder Ashkenazi Jewish variant associated with telomere biology disorders

npj Genomic Medicine(2025)10.1038/s41525-025-00501-8

N/A

0.104DataRank · unranked

1 citations

Emília M. Pinto, Tianna Zhao, Logan P Zeigler, Jung Kim, Neelam Giri +18 more

A literature review and pooled case analysis of cardiofaciocutaneous syndrome to estimate cancer risk

Genetics in Medicine(2025)10.1016/j.gim.2025.101423

N/A

0.104DataRank · unranked

1 citations

Toniya Brown, Sonia Bhala, Anaqa Faizer, Muzzammil Ahmadzada, Alicia A. Livinski +6 more

Congenital anomalies and health outcomes among survivors of childhood cancer: A report from the childhood cancer survivor study.

Journal of Clinical Oncology(2023)10.1200/jco.2023.41.16_suppl.e22021

N/A

0DataRank · unranked

0 citations

Weiyu Qiu, Jeremy M. Schraw, Sogol Mostoufi‐Moab, Lisa Mirabello, Douglas R. Stewart +9 more

Investigation of cancer predisposition in Fanconi anemia heterozygotes: A DiscovEHR cohort population study.

Journal of Clinical Oncology(2023)10.1200/jco.2023.41.16_suppl.10589

N/A

0DataRank · unranked

0 citations

Burak Altintas, Jeremy S. Haley, Jung Kim, David J. Carey, Douglas R. Stewart +2 more

Genome‐wide association study of café‐au‐lait macule number in neurofibromatosis type 1

Molecular Genetics & Genomic Medicine(2020)10.1002/mgg3.1400

N/A

0DataRank · unranked

5 citations

Paula L. Hyland, Alexander Pemov, Jeremy Sabourin, Andrea Baldwin, Sara Bass +6 more

Data underlying OpenPBTA Manuscript Figures and Molecular Alterations

Zenodo (CERN European Organization for Nuclear Research)(2023)10.5281/zenodo.7877739

Top 100%

0DataRank

Top 100%0 citations

Krutika S. Gaonkar, Stephanie J. Spielman, Candace L. Savonen, Chanté J. Bethell, Run Jin +63 more

DICER1-Related Tumor Predisposition: Identification of At-risk Individuals and Recommended Surveillance Strategies

Clinical Cancer Research(2024)10.1158/1078-0432.ccr-24-1532

N/A

0DataRank · unranked

29 citations

Alexander T. Nelson, Paige Mallinger, Anne K. Harris, Junne Kamihara, Shari Baldinger +26 more

Data underlying OpenPBTA Manuscript Figures and Molecular Alterations

Zenodo (CERN European Organization for Nuclear Research)(2023)10.5281/zenodo.7805408

Top 100%

0DataRank

Top 100%0 citations

Krutika S. Gaonkar, Stephanie J. Spielman, Candace L. Savonen, Chanté J. Bethell, Run Jin +63 more

Figure S2 from Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition

Figshare(2025)10.1158/1078-0432.29052955

N/A

0DataRank · unranked

0 citations

Lisa Golmard, Jung Kim, Riyue Bao, Frank Y. Lin, Angshumoy Roy +32 more

Germline Genetic Testing and Survival Outcomes Among Children With Rhabdomyosarcoma

JAMA Network Open(2024)10.1001/jamanetworkopen.2024.4170

N/A

0DataRank · unranked

13 citations

He Li, Michael E. Scheurer, Dana L. Casey, Shannon Dugan‐Perez, Deborah A. Marquez-Do +19 more

Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2024)10.1016/j.gim.2024.101142

N/A

0DataRank · unranked

13 citations

Kristy Lee, Noura S. Abul‐Husn, Laura M. Amendola, Kyle B. Brothers, Wendy K. Chung +8 more

Issue Information

Human Mutation(2018)10.1002/humu.23568

N/A

0DataRank · unranked

0 citations

R. Donald Harvey, Tracy Dudding‐Byth, Liliana Catherine Patiño, Isabelle Beau, Adrien Morel +135 more

Figure S3 from Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition

Figshare(2025)10.1158/1078-0432.29052952

N/A

0DataRank · unranked

0 citations

Lisa Golmard, Jung Kim, Riyue Bao, Frank Y. Lin, Angshumoy Roy +32 more

Figure S1 from Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition

(2025)10.1158/1078-0432.29052958

N/A

0DataRank · unranked

0 citations

Lisa Golmard, Jung Kim, Riyue Bao, Frank Y. Lin, Angshumoy Roy +32 more

Supplementary Table Legend 1 from Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition

Figshare(2025)10.1158/1078-0432.29052940

N/A

0DataRank · unranked

0 citations

Lisa Golmard, Jung Kim, Riyue Bao, Frank Y. Lin, Angshumoy Roy +32 more

Genome-wide investigation of rare germline copy-number variants in retinoblastoma

medRxiv(2024)10.1101/2024.11.19.24316720

N/A

0DataRank · unranked

0 citations

Jung Kim, Jazmyn Bess, Sungduk Kim, Paul S. Albert, Nathalie Japkowicz +3 more

Germline Genetic Testing and Survival Outcomes Among Children With Rhabdomyosarcoma

UNC Libraries(2024)10.17615/m7sp-3e70

N/A

0DataRank · unranked

0 citations

Shannon Dugan‐Perez, Michael E. Scheurer, Sharon E. Plon, Brian D. Crompton, Philip J. Lupo +19 more

ACMG SF v3.3 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2025)10.1016/j.gim.2025.101454

N/A

0DataRank · unranked

56 citations

Noura S. Abul‐Husn, Laura M. Amendola, Kyle B. Brothers, Wendy K. Chung, Michael H. Gollob +11 more

Supplementary Data 1 from Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition

Figshare(2025)10.1158/1078-0432.29052943

Top 100%

0DataRank

Top 100%0 citations

Lisa Golmard, Jung Kim, Riyue Bao, Frank Y. Lin, Angshumoy Roy +32 more

Management of individuals with heterozygous germline pathogenic variants in RAD51C, RAD51D, and BRIP1: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2025)10.1016/j.gim.2025.101557

N/A

0DataRank · unranked

5 citations

Jianbang Chiang, Esteban Astiazarán-Symonds, Judith Balmañà, Ilana Cass, F. Kommoss +13 more

Symposium report—ethical and social considerations regarding return of secondary findings in atomic bomb survivors

Carcinogenesis(2025)10.1093/carcin/bgaf059

N/A

0DataRank · unranked

2 citations

Douglas R. Stewart, Arikuni Uchimura, Ken-ichi Arita, Yvonne Bombard, Megan N. Frone +18 more

Management of individuals with germline pathogenic/likely pathogenic variants in CHEK2: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2023)10.1016/j.gim.2023.100870

N/A

0DataRank · unranked

83 citations

Esteban Astiazarán-Symonds, Laura M. Amendola, Judith Balmañà, William D. Foulkes, Paul A. James +9 more

Prolonged Heparin Re‐Exposure in a Patient With Previous Heparin‐Induced Thrombocytopenia ( HIT )

International Journal of Laboratory Hematology(2025)10.1111/ijlh.14552

N/A

0DataRank · unranked

0 citations

Gina M. Ney, Khanh Nghiem, Shelley S. Kalsi, Charles D. Bolan, Katherine R. Calvo +8 more

Cancer in Costello syndrome: a systematic review and meta-analysis

British Journal of Cancer(2023)10.1038/s41416-023-02229-7

N/A

0DataRank · unranked

21 citations

Gina M. Ney, Cecilia Higgs, Leatrisse Oba, Radhika Srivastava, Alicia A. Livinski +3 more

ALT in Pediatric High-Grade Gliomas Can Occur without ATRX Mutation and is Enriched in Patients with Pathogenic Germline MMR Variants

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.08.05.502870

N/A

0DataRank · unranked

0 citations

Heba Ijaz, Krutika S. Gaonkar, Rebecca S. Kaufman, Run Jin, Anastasios Karras +18 more

Examination of Genetic Susceptibility in Radiation-Associated Meningioma

Radiation Research(2022)10.1667/rade-21-00035.1

N/A

0DataRank · unranked

0 citations

JONG HUN Kim, Kristine Jones, Aurélie Vogt, Siegal Sadetzki, Douglas R. Stewart +1 more

Cancer incidence and surveillance strategies in individuals withRASopathies

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2022)10.1002/ajmg.c.32018

N/A

0DataRank · unranked

25 citations

Andrea M. Gross, Alicia A. Livinski, Christian P. Kratz, Douglas R. Stewart, Gina M. Ney

Type I and Ir pleuropulmonary blastoma (PPB): A report from the International PPB/DICER1 Registry

Cancer(2022)10.1002/cncr.34593

N/A

0DataRank · unranked

24 citations

Anne K. Harris, Dave Watson, Doug Miniati, Mike Finch, Junne Kamihara +15 more

Douglas R. Stewart

Indexed papers

Top data-sharing exemplar

Papers