Daniel L. Van Dyke

7.7k citations

183 papers · 4.7k indexed · h-index 41

Co-authors: Lester Weiss Anne E. Wiktor V. Ramesh Babu Ayalew Tefferi Curtis A. Hanson Thomas E. Carey Neil E. Kay Maria J. Worsham
Topics: Genomic variations and chromosomal abnormalities (59 papers)Chronic Lymphocytic Leukemia Research (34 papers)Acute Myeloid Leukemia Research (31 papers)
Cited by: Genetics Hematology
Journals: Proceedings of the National Academy of Sciences JAMA Blood
Partner nations: United States Italy Canada

In The Last Decade

Daniel L. Van Dyke

177 papers receiving 4.6k citations

Peers

Countries citing papers authored by Daniel L. Van Dyke

Since Specialization

Citations

This map shows the geographic impact of Daniel L. Van Dyke's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Daniel L. Van Dyke with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel L. Van Dyke more than expected).

Fields of papers citing papers by Daniel L. Van Dyke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel L. Van Dyke. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Daniel L. Van Dyke. The network helps show where Daniel L. Van Dyke may publish in the future.

Co-authorship network of co-authors of Daniel L. Van Dyke

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel L. Van Dyke. A scholar is included among the top collaborators of Daniel L. Van Dyke based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Daniel L. Van Dyke. Daniel L. Van Dyke is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Utility of Targeted Sequencing Compared to FISH for Detection of Chronic Lymphocytic Leukemia Copy Number Alterations 2024 ·Cancers ·(unknown),(unknown),Daniel R. O’Brien,Erik Jessen,Cecília Bonolo de Campos,Nicholas Boddicker,(unknown),Cristine Allmer,Kari G. Rabe,James R. Cerhan,Sameer A. Parikh,Neil E. Kay,Huihuang Yan,Daniel L. Van Dyke,Susan L. Slager,Esteban Braggio	2
2	Assessing copy number aberrations and copy-neutral loss-of-heterozygosity across the genome as best practice: An evidence-based review from the Cancer Genomics Consortium (CGC) working group for chronic lymphocytic leukemia 2018 ·Cancer Genetics ·Kathy Chun,Gail D. Wenger,Alka Chaubey,Durga Prasad Dash,Rashmi Kanagal‐Shamanna,Sibel Kantarci,Ravindra Kolhe,Daniel L. Van Dyke,Lu Wang,Daynna J. Wolff,Patricia M. Miron	20
3	When are apparently non-clonal abnormalities in bone marrow chromosome studies actually clonal? 2012 ·Cancer Genetics ·(unknown),Rhett P. Ketterling,Daniel L. Van Dyke	2
4	Stimulation of chronic lymphocytic leukemia cells with CpG oligodeoxynucleotide gives consistent karyotypic results among laboratories: a CLL Research Consortium (CRC) Study 2010 ·Cancer Genetics and Cytogenetics ·Nyla A. Heerema,John C. Byrd,(unknown),(unknown),Prasad Koduru,Ayala Aviram,Stephanie A. Smoley,Laura Z. Rassenti,Andrew Greaves,Jennifer R. Brown,R. Kanti,Thomas J. Kipps,Neil E. Kay,Daniel L. Van Dyke	38
5	Refined cytogenetic-risk categorization for overall and leukemia-free survival in primary myelofibrosis: a single center study of 433 patients 2010 ·Leukemia ·Domenica Caramazza,Kebede H. Begna,Naseema Gangat,Rakhee Vaidya,S. Siragusa,Daniel L. Van Dyke,Curtis A. Hanson,Animesh Pardanani,Ayalew Tefferi	119
6	De novo deletion 17p13.1 chronic lymphocytic leukemia shows significant clinical heterogeneity: the M. D. Anderson and Mayo Clinic experience 2009 ·Blood ·Constantine S. Tam,Tait D. Shanafelt,William G. Wierda,Lynne V. Abruzzo,Daniel L. Van Dyke,Susan O’Brien,Alessandra Ferrajoli,Susan Lerner,Alice Lynn,Neil E. Kay,Michael J. Keating	114
7	Dosage Regulation of the Active X Chromosome in Human Triploid Cells 2009 ·PLoS Genetics ·Xinxian Deng,Di Kim Nguyen,R. Scott Hansen,Daniel L. Van Dyke,Stanley M. Gartler,Christine M. Distèche	15
8	FISH analysis helps identify low-level mosaicism in Ullrich-Turner syndrome patients 2004 ·Genetics in Medicine ·Anne E. Wiktor,Daniel L. Van Dyke	19
9	PRDX4, a member of the peroxiredoxin family, is fused to AML1 (RUNX1) in an acute myeloid leukemia patient with a t(X;21)(p22;q22) 2004 ·Genes Chromosomes and Cancer ·Yanming Zhang,(unknown),(unknown),Jianjun Chen,Muhammad Shurafa,Daniel L. Van Dyke,Anne E. Wiktor,Janet D. Rowley	31
10	Diagnostic testing for Prader-Willi syndrome and Angelman syndrome: A cost comparison 2002 ·Genetics in Medicine ·Kristin G. Monaghan,Anne E. Wiktor,Daniel L. Van Dyke	9
11	Prenatal diagnosis of 22q11.2 deletion when ultrasound examination reveals a heart defect 2001 ·Genetics in Medicine ·(unknown),Jacquelyn Roberson,Anne E. Wiktor,(unknown),(unknown),(unknown),Daniel L. Van Dyke	17
12	Duplication 6q21q23 in two unrelated patients 1998 ·American Journal of Medical Genetics ·Victoria M. Pratt,Jacquelyn Roberson,Lester Weiss,Daniel L. Van Dyke	10
13	INCIDENCE AND SIGNIFICANCE OF CHROMOSOME MOSAICISM INVOLVING AN AUTOSOMAL STRUCTURAL ABNORMALITY DIAGNOSED PRENATALLY THROUGH AMNIOCENTESIS: A COLLABORATIVE STUDY 1996 ·Prenatal Diagnosis ·Lillian Y. F. Hsu,(unknown),K Richkind,Daniel L. Van Dyke,Barbara F. Crandall,Debra Saxe,Gabriel S. Khodr,Michael T. Mennuti,Gail Stetten,Wayne A. Miller,Jean H. Priest	80
14	Common clonal origin of synchronous primary head and neck squamous cell carcinomas: Analysis by tumor karyotypes and fluorescence in situ hybridization 1995 ·Human Pathology ·Maria J. Worsham,Sandra R. Wolman,Thomas E. Carey,Richard J. Zarbo,Michael S. Benninger,Daniel L. Van Dyke	82
15	Ullrich‐Turner syndrome with a small ring X chromosome and presence of mental retardation 1992 ·American Journal of Medical Genetics ·Daniel L. Van Dyke,Anne E. Wiktor,(unknown),Dorothy A. Miller,Michał Witt,V. Ramesh Babu,Maria J. Worsham,Jacquelyn Roberson,Lester Weiss	72
16	Mother and son with deletion of 3p25‐pter 1991 ·American Journal of Medical Genetics ·(unknown),Jacquelyn Roberson,Daniel L. Van Dyke,V. Ramesh Babu,Lester Weiss	18
17	Consistent Chromosome Abnormalities in Squamous Cell Carcinoma of the Vulva 1991 ·Genes Chromosomes and Cancer ·Maria J. Worsham,Daniel L. Van Dyke,Seija Grénman,Reidar Grénman,Michael P. Hopkins,James A. Roberts,(unknown),Donald R. Schwartz,Thomas E. Carey	58
18	Secondary trisomy or mosaic “tetrasomy” 8p 1989 ·American Journal of Medical Genetics ·Meinhard Robinow,(unknown),(unknown),(unknown),Daniel L. Van Dyke,V. Ramesh Babu,(unknown),(unknown),(unknown),(unknown)	20
19	Cytogenetic studies of cryptorchid testes 1977 ·Lester Weiss,Richard C. Klugo,Daniel L. Van Dyke	2
20	Thyroid abnormalities in 20 children with Turner syndrome 1977 ·The Journal of Pediatrics ·G. Shashidhar Pai,David C. Leach,Lester Weiss,(unknown),Daniel L. Van Dyke	37

About Daniel L. Van Dyke

Daniel L. Van Dyke is a scholar working on Genetics, Genetics and Hematology, having authored 183 papers that have together received 4.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (59 papers), Chronic Lymphocytic Leukemia Research (34 papers) and Acute Myeloid Leukemia Research (31 papers). The work is most often cited by research in Genetics (1.4k citations), Hematology (925 citations) and Genetics (1.9k citations). Daniel L. Van Dyke has collaborated with scholars based in United States, Italy and Canada. Frequent co-authors include Lester Weiss, Anne E. Wiktor, V. Ramesh Babu, Ayalew Tefferi, Curtis A. Hanson, Thomas E. Carey, Neil E. Kay, Maria J. Worsham, Animesh Pardanani and Benjamin A. Rybicki. Their work appears in journals such as Proceedings of the National Academy of Sciences, JAMA and Blood.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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