Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

K. Krysiak · SciRah

Researcher profile · Semantic Scholar

K. Krysiak

Share profile

K. Krysiak — researcher profile on SciRah

h-index: 24
Works: 164
Citations: 3,880

Most-cited papers

Standards for the Classification of Pathogenicity of Somatic Variants in Cancer (Oncogenicity): Joint Recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)
P. Horák, M. Griffith, Arpad M. Danos, B. Pitel +43 more
2022Genetics in Medicine231 citations Open access
Semantic Scholar
A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer
A. Wagner, B. Walsh, Georgia Mayfield, D. Tamborero +35 more
2020Nature Genetics142 citations Open access
Semantic Scholar
CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase
K. Krysiak, Arpad M. Danos, J. Saliba, Joshua F. McMichael +61 more
2022Nucleic Acids Res.40 citations Open access
Semantic Scholar
Phase I/Dose Expansion Trial of Brentuximab vedotin/Lenalidomide in Relapsed or Refractory Diffuse Large B-cell Lymphoma.
J. Ward, M. Berrien-Elliott, Felicia Gomez, Jingqin R Luo +16 more
2021Blood31 citations Open access
Semantic Scholar
Mutations associated with progression in follicular lymphoma predict inferior outcomes at diagnosis: Alliance A151303
D. Russler-Germain, K. Krysiak, Cody A. Ramirez, Matthew Mosior +19 more
2023Blood Advances24 citations Open access
Semantic Scholar
Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).
P. Horák, M. Griffith, Arpad M. Danos, B. Pitel +43 more
2022Genetics in Medicine23 citations Open access
Semantic Scholar
Large scale genotype- and phenotype-driven machine learning in Von Hippel-Lindau disease
Andreea Chiorean, K. Farncombe, Sean Delong, Veronica Andric +21 more
2022Human Mutation17 citations Open access
Semantic Scholar
Neoantigen landscape supports feasibility of personalized cancer vaccine for follicular lymphoma
Cody A. Ramirez, M. Becker-Hapak, K. Singhal, D. Russler-Germain +29 more
2022medRxiv15 citations Open access
Semantic Scholar
A community approach to the cancer variant interpretation bottleneck
K. Krysiak, Arpad M. Danos, Susanna Kiwala, Joshua F. McMichael +48 more
2022Nature Cancer12 citations Open access
Semantic Scholar
Ultra-Deep Sequencing Reveals the Mutational Landscape of Classical Hodgkin Lymphoma
Felicia Gomez, Bryan Fisk, Joshua F. McMichael, Matthew Mosior +27 more
2021medRxiv12 citations Open access
Semantic Scholar
Impact of a 40-Gene Targeted Panel Test on Physician Decision Making for Patients With Acute Myeloid Leukemia
Erica K. Barnell, Kenneth F. Newcomer, Zachary L. Skidmore, K. Krysiak +21 more
2021JCO Precision Oncology10 citations Open access
Semantic Scholar
Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers
Zachary L. Skidmore, J. Kunisaki, Yiing Lin, Kelsy C. Cotto +14 more
2022Cancer Genetics7 citations Open access
Semantic Scholar
A Comparative Analysis of RAS Variants in Patients with Disorders of Somatic Mosaicism.
Y. Hou, Michael J. Evenson, M. Corliss, L. Mahapatra +19 more
2022Genetics in Medicine7 citations Open access
Semantic Scholar
Modified Rules for Classification of Variants Associated With Disorders of Somatic Mosaicism
Fernando Zazueta Leon-Quintero, Kevin M. Bowling, Alexa Dickson, M. Corliss +7 more
2024Clinical Genetics6 citations Open access
Semantic Scholar
Heterozygous HMGB1 loss‐of‐function variants are associated with developmental delay and microcephaly
K. Uguen, K. Krysiak, S. Audebert-Bellanger, S. Redon +24 more
2021Clinical Genetics6 citations
Semantic Scholar
Haploinsufficiency of multiple del(5q) genes induce B cell abnormalities in mice
Tuo-En Liu, Tanzir Ahmed, K. Krysiak, C. Shirai +7 more
2020Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis6 citations Open access
Semantic Scholar
Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers
Zachary L. Skidmore, J. Kunisaki, Yiing Lin, Kelsy C. Cotto +14 more
2021bioRxiv5 citations Open access
Semantic Scholar
Accessing clinical-grade genomic classification data through the ClinGen Data Platform
Karen P. Dalton, H. Rehm, Matt W. Wright, Mark E. Mandell +5 more
2022Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing4 citations Open access
Semantic Scholar
Evaluating Language Models for Biomedical Fact-Checking: A Benchmark Dataset for Cancer Variant Interpretation Verification
C. Reisle, Cameron J. Grisdale, K. Krysiak, Arpad M. Danos +12 more
2025bioRxiv3 citations Open access
Semantic Scholar
Comprehensive Analysis of TEK Variants in Patients With Vascular Malformations
Reza Ghasemi, M. Corliss, Kevin M. Bowling, K. Krysiak +7 more
2024Clinical Genetics3 citations
Semantic Scholar
Multi-Platform Curation in the Development of ACMG/AMP Specifications for Von Hippel-Lindau (VHL) Disease
Deborah I. Ritter, C. Badduke, K. Doonanco, H. Kang +23 more
2026Genetics in Medicine2 citations Open access
Semantic Scholar
Multi-Platform Curation in the Development of ACMG/AMP Specifications for Von Hippel Lindau (VHL) Disease
D. Ritter, C. Badduke, K. Doonanco, Hc Kang +23 more
2025medRxiv1 citations Open access
Semantic Scholar
35. Evolution of a variant curation procedures in the open-access cancer variant interpretation knowledgebase CIViC
K. Krysiak, Arpad M. Danos, J. Saliba, Susanna Kiwala +7 more
2023Cancer Genetics1 citations
Semantic Scholar
16. Enhancement of pediatric cancer curation and representation through expert-guided data mining and ontology refinement
J. Saliba, Jake Lever, K. Krysiak, Lana M. Sheta +19 more
2022Cancer Genetics1 citations
Semantic Scholar
Abstract 1193: Enhancing pediatric cancer variant curation and representation through standardized classification and automation
J. Saliba, Jake Lever, K. Krysiak, Arpad M. Danos +17 more
2022Cancer Research1 citations
Semantic Scholar
Mutations Associated with Progression in Follicular Lymphoma Predict Inferior Outcomes in Newly Diagnosed Patients (Alliance 151303)
D. Russler-Germain, K. Krysiak, Cody A. Ramirez, Matthew Mosior +17 more
2022Blood1 citations Open access
Semantic Scholar
20. A resource for our clinical genomics community: The Compendium of Cancer Genome Aberrations (CCGA)
J. Hodge, B. Pitel, B. Davis, L. Cooley +10 more
2020Cancer Genetics1 citations
Semantic Scholar
Searching the Druggable Genome using Large Language Models
Lars Schimmelpfennig, M. Cannon, Quentin Cody, Joshua F. McMichael +6 more
2026bioRxiv0 citations Open access
Semantic Scholar
P562: The diagnostic yield of clinical testing for somatic variation in cortical malformations and epilepsy*
R. Duan, M. Corliss, Kevin M. Bowling, Jason Walker +6 more
2026Genetics in Medicine Open0 citations Open access
Semantic Scholar
Exome sequencing of Hodgkin and non-Hodgkin composite lymphomas identifies shared somatic mutations indicative of common founding precursors
Felicia Gomez, L. Shea, S. Sharavanan, D. Russler-Germain +15 more
2026Cancer Genetics0 citations
Semantic Scholar
Searching the druggable genome using large language models
Lars Schimmelpfennig, M. Cannon, Quentin Cody, Joshua F. McMichael +6 more
2026Bioinformatics0 citations Open access
Semantic Scholar
P631: Clinical utility of rapid genome sequencing in pediatric patients with cardiac phenotypes
Kevin M. Bowling, Matheus Vernet Machado Bressan Wilke, Michelle Thompson, Alexa Dickson +19 more
2026Genetics in Medicine Open0 citations Open access
Semantic Scholar
P592: Diagnostic utility of next-generation sequencing for somatic mosaicism: Insights from routine clinical practice
R. Mikaeel, M. Corliss, Kevin M. Bowling, K. Krysiak +5 more
2026Genetics in Medicine Open0 citations Open access
Semantic Scholar
P801: Low-level somatic convoluted indel variants in C-terminal region of TEK revealed by deep sequencing on patients with vascular malformations
R. Duan, Alexa Dickson, M. Corliss, K. Krysiak +3 more
2025Genetics in Medicine Open0 citations Open access
Semantic Scholar
Tailored Approaches in the Treatment of Patients With Colorectal Cancer Harboring Tropomyosin Receptor Kinase Fusion and Microsatellite Instability-High: A Case Report and Literature Review.
Samuel Kim, Malak Itani, Xiuli Liu, Lulu Sun +13 more
2025JCO Precision Oncology0 citations
Semantic Scholar
66. Progress and future of the Compendium of Cancer Genome Aberrations (CCGA)
Jennelle C. Hodge, Eric McGinnis, Sumire Kitahara, Fabiola Quintero-Rivera +24 more
2025Cancer Genetics0 citations
Semantic Scholar
P715: Testing indications and diagnostic yield of clinical exome sequencing in a US Midwestern patient cohort
Michelle Thompson, Mathues Vernet Machado Bressan Wilke, Alexa Dickson, M. Corliss +9 more
2025Genetics in Medicine Open0 citations Open access
Semantic Scholar
50. Updates to the CIViC knowledgebase: The fusion feature type
Arpad M. Danos, K. Krysiak, Saliba Jason, Adam C. Coffman +9 more
2025Cancer Genetics0 citations
Semantic Scholar
80. Integrating expert knowledge for somatic variant interpretation: Achievements and future directions of ClinGen somatic
J. Saliba, Arpad M. Danos, K. Krysiak, Adam C. Coffman +24 more
2025Cancer Genetics0 citations Open access
Semantic Scholar
7. Application of expert panel-derived oncogenicity guidelines in BCR::ABL1-like B-lymphoblastic leukemia/lymphoma
Mark G. Evans, K. Krysiak, J. Saliba, C. Kesserwan +35 more
2025Cancer Genetics0 citations
Semantic Scholar
A prospective Study of whole genome sequencing for genomic profiling and risk determination in MDS
R. de Jesus, Samuel Urrutia, David Spencer, Eric Duncavage +9 more
2025Blood0 citations
Semantic Scholar
P324: Research analysis of clinical exome sequence data to detect diabetes-related genetic variation
Matheus Wilke, Matheus Vernet Machado Bressan Wilke, Michelle Thompson, S. Jho +13 more
2025Genetics in Medicine Open0 citations Open access
Semantic Scholar
Improving diagnostic accuracy for hematologic malignancies: the impact of clear test nomenclature on BCR::ABL1 test ordering in electronic medical records
P. Hernandez, K. Krysiak, B. Parikh, Ronald Jackups
2025Journal of Pathology Informatics0 citations Open access
Semantic Scholar
41. Step 2 updates for the oncogenic assessment of FLT3 variants by the ClinGen FLT3 somatic cancer variant curation expert
Nathan Kopp, Mani Coumarane, Rong He, Yuwen Li +14 more
2024Cancer Genetics0 citations
Semantic Scholar
28. Addition of non-gene features to the CIViC data model
Arpad M. Danos, K. Krysiak, Adam C. Coffman, Joshua F. McMichael +5 more
2024Cancer Genetics0 citations
Semantic Scholar
57. Developing oncogenicity guidelines for BCR::ABL1-like B-lymphoblastic leukemia/lymphoma through expert consensus
K. Krysiak, J. Saliba, C. Kesserwan, Yassmine M. N. Akkari +34 more
2024Cancer Genetics0 citations
Semantic Scholar
1. Enrichment of Hodgkin and Reed-Sternberg (HRS) cells using size-based microfiltration
Brianna Munnich, K. Krysiak, B. Brown, Richard Cote +5 more
2024Cancer Genetics0 citations Open access
Semantic Scholar
54. Creation of a knowledgebase of high-quality assertions of the clinical actionability of somatic variants in cancer
J. Saliba, Arpad M. Danos, K. Krysiak, Adam C. Coffman +24 more
2024Cancer Genetics0 citations
Semantic Scholar
40. Prioritization of defining and supportive diagnostic variants in pediatric tumors
Laura B. Corson, J. Saliba, L. Satgunaseelan, Dianne E. Sylvester +20 more
2024Cancer Genetics0 citations
Semantic Scholar
25. Enhancing precision oncology: The value of open-source knowledgebase integration
Cameron J. Grisdale, E. Pleasance, Connor Frey, C. Reisle +21 more
2024Cancer Genetics0 citations
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

M. Griffith×31
Invite
M. Griffith — researcher profile on SciRah
O. Griffith×30
Invite
O. Griffith — researcher profile on SciRah
Arpad M. Danos×18
Invite
Arpad M. Danos — researcher profile on SciRah
J. Saliba×14
Invite
J. Saliba — researcher profile on SciRah

×13

Invite

A. Wagner — researcher profile on SciRah

Invite

G. Raca — researcher profile on SciRah

Joshua F. McMichael×12

Invite

Joshua F. McMichael — researcher profile on SciRah

Adam C. Coffman×10

Invite

Adam C. Coffman — researcher profile on SciRah

Susanna Kiwala×10

Invite

Susanna Kiwala — researcher profile on SciRah

Cameron J. Grisdale×10

Invite

Cameron J. Grisdale — researcher profile on SciRah

Julie A. Neidich×10

Invite

Julie A. Neidich — researcher profile on SciRah

Invite

M. Corliss — researcher profile on SciRah