Daniel Dykas

1.1k total citations
15 papers, 681 citations indexed

About

Daniel Dykas is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Daniel Dykas has authored 15 papers receiving a total of 681 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Epidemiology. Recurrent topics in Daniel Dykas's work include Liver Disease Diagnosis and Treatment (5 papers), Genomics and Rare Diseases (4 papers) and Diet, Metabolism, and Disease (3 papers). Daniel Dykas is often cited by papers focused on Liver Disease Diagnosis and Treatment (5 papers), Genomics and Rare Diseases (4 papers) and Diet, Metabolism, and Disease (3 papers). Daniel Dykas collaborates with scholars based in United States, Italy and Sweden. Daniel Dykas's co-authors include A. Bale, Nicola Santoro, Sonia Caprio, Bridget Pierpont, Melissa Shaw, Hongyu Zhao, Romy Kursawe, Roger D. Klein, Leif Groop and A.J. Pakstis and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Hepatology.

In The Last Decade

Daniel Dykas

13 papers receiving 662 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Daniel Dykas United States	9	423	284	140	133	121	15	681
Giorgio Zanette Italy	12	228 0.5×	306 1.1×	116 0.8×	63 0.5×	335 2.8×	21	812
Eduardo Larrañaga Spain	10	221 0.5×	170 0.6×	31 0.2×	29 0.2×	96 0.8×	32	470
Kazuhiro Kashiwagi Japan	17	143 0.3×	46 0.2×	93 0.7×	27 0.2×	102 0.8×	46	617
Stephan Buch Germany	14	236 0.6×	100 0.4×	54 0.4×	15 0.1×	169 1.4×	32	661
Jung‐Min Lee South Korea	11	206 0.5×	127 0.4×	34 0.2×	33 0.2×	148 1.2×	37	526
Takehisa Suekane Japan	11	137 0.3×	42 0.1×	45 0.3×	31 0.2×	89 0.7×	28	401
Ryan S. Huss United States	9	368 0.9×	156 0.5×	13 0.1×	26 0.2×	126 1.0×	16	523
Travis Monchamp United States	6	181 0.4×	418 1.5×	420 3.0×	47 0.4×	201 1.7×	8	915
Elaine Drobny United States	8	116 0.3×	116 0.4×	113 0.8×	18 0.1×	99 0.8×	10	511
George Philips United States	6	193 0.5×	29 0.1×	59 0.4×	17 0.1×	133 1.1×	12	464

Countries citing papers authored by Daniel Dykas

Since Specialization

Citations

This map shows the geographic impact of Daniel Dykas'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 Dykas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel Dykas more than expected).

Fields of papers citing papers by Daniel Dykas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel Dykas. 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 Dykas. The network helps show where Daniel Dykas may publish in the future.

Co-authorship network of co-authors of Daniel Dykas

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel Dykas. A scholar is included among the top collaborators of Daniel Dykas 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 Dykas. Daniel Dykas is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

Abdelhamed, Zakia, et al.. (2024). P602: Genetic modifiers as a basis for phenotypic variability in mosaic trisomy 8. SHILAP Revista de lepidopterología. 2. 101508–101508.

Zafar, Mohammad A., Deqiong Ma, Hui Zhang, et al.. (2024). Somatic Variants Acquired Later in Life Associated with Thoracic Aortic Aneurysms: JAK2 V617F. Genes. 15(7). 883–883.

Hakim, Aaron, Aimée M. Deaton, Lucas D. Ward, et al.. (2023). Advancing diagnosis and management of liver disease in adults through exome sequencing. EBioMedicine. 95. 104747–104747. 12 indexed citations

Towne, Meghan C., Daniel Dykas, Armin Attar, et al.. (2022). Abstract 554: The Association Of Multiple Variants In The TNXB Gene With Vascular Aneurysms And Dissections. Arteriosclerosis Thrombosis and Vascular Biology. 42(Suppl_1). 1 indexed citations

Wen, Jiadi, Hongyan Chai, Daniel Dykas, et al.. (2022). Detecting regions of homozygosity improves the diagnosis of pathogenic variants and uniparental disomy in pediatric patients. American Journal of Medical Genetics Part A. 188(6). 1728–1738. 1 indexed citations

Hakim, Aaron, Xuchen Zhang, Elif A Oral, et al.. (2019). Clinical utility of genomic analysis in adults with idiopathic liver disease. Journal of Hepatology. 70(6). 1214–1221. 49 indexed citations

Gulati, Ashima, A. Bale, Daniel Dykas, et al.. (2018). TREX1 Mutation Causing Autosomal Dominant Thrombotic Microangiopathy and CKD—A Novel Presentation. American Journal of Kidney Diseases. 72(6). 895–899. 12 indexed citations

Umano, Giuseppina Rosaria, Sonia Caprio, Anna Di Sessa, et al.. (2018). The rs626283 Variant in the MBOAT7 Gene is Associated with Insulin Resistance and Fatty Liver in Caucasian Obese Youth. The American Journal of Gastroenterology. 113(3). 376–383. 47 indexed citations

Seidelmann, Sara B., Emily Smith, Lakshman Subrahmanyan, et al.. (2017). Application of Whole Exome Sequencing in the Clinical Diagnosis and Management of Inherited Cardiovascular Diseases in Adults. Circulation Cardiovascular Genetics. 10(1). 38 indexed citations

10.

Ziganshin, Bulat A., Daniel Dykas, Paris Charilaou, et al.. (2015). Routine Genetic Testing for Thoracic Aortic Aneurysm and Dissection in a Clinical Setting. The Annals of Thoracic Surgery. 100(5). 1604–1611. 92 indexed citations

11.

Lee, Eun‐Ju, Daniel Dykas, A. Bale, et al.. (2015). Whole Exome Sequencing in Evaluation of Thrombophilia: A Novel 33-Gene Panel. Blood. 126(23). 3529–3529. 1 indexed citations

12.

Santoro, Nicola, Hongyu Zhao, A.J. Pakstis, et al.. (2011). Variant in the glucokinase regulatory protein ( GCKR ) gene is associated with fatty liver in obese children and adolescents. Hepatology. 55(3). 781–789. 194 indexed citations

13.

Santoro, Nicola, Romy Kursawe, Ebe D’Adamo, et al.. (2010). A Common Variant in the Patatin-Like Phospholipase 3 Gene ( PNPLA3 ) Is Associated with Fatty Liver Disease in Obese Children and Adolescents. Hepatology. 52(4). 1281–1290. 178 indexed citations

14.

Klein, Roger D., Erik C. Thorland, Patrick R. Gonzales, et al.. (2006). A Multiplex Assay for the Detection and Mapping of Complex Glycerol Kinase Deficiency. Clinical Chemistry. 52(10). 1864–1870. 5 indexed citations

15.

Klein, Roger D., Daniel Dykas, & A. Bale. (2005). Clinical testing for the nevoid basal cell carcinoma syndrome in a DNA diagnostic laboratory. Genetics in Medicine. 7(9). 611–619. 51 indexed citations

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.

Explore authors with similar magnitude of impact