Kent E. Kruckeberg

438 total citations
9 papers, 350 citations indexed

About

Kent E. Kruckeberg is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Kent E. Kruckeberg has authored 9 papers receiving a total of 350 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Genetics and 2 papers in Hematology. Recurrent topics in Kent E. Kruckeberg's work include Genetics and Neurodevelopmental Disorders (2 papers), Trace Elements in Health (2 papers) and Hemoglobinopathies and Related Disorders (2 papers). Kent E. Kruckeberg is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Trace Elements in Health (2 papers) and Hemoglobinopathies and Related Disorders (2 papers). Kent E. Kruckeberg collaborates with scholars based in United States. Kent E. Kruckeberg's co-authors include Stephen N. Thibodeau, Daniel J. Schaid, David J. Tester, Karen Snow, David J. Brandhagen, Narasimhan Nagan, Piero Rinaldo, Michael K. Porayko, William Alvarez and Jürgen Ludwig and has published in prestigious journals such as Hepatology, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

In The Last Decade

Kent E. Kruckeberg

9 papers receiving 338 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kent E. Kruckeberg United States	8	180	132	62	54	53	9	350
Lilia Romdhane Tunisia	12	150 0.8×	189 1.4×	19 0.3×	37 0.7×	6 0.1×	29	394
Konstantina Kosma Greece	10	130 0.7×	137 1.0×	19 0.3×	28 0.5×	21 0.4×	30	288
Abelardo Solano Spain	11	265 1.5×	52 0.4×	11 0.2×	15 0.3×	6 0.1×	14	407
Selwa A.F. Al-Hazzaa Saudi Arabia	10	112 0.6×	71 0.5×	10 0.2×	41 0.8×	9 0.2×	27	365
Kaplan Jc France	12	185 1.0×	67 0.5×	16 0.3×	36 0.7×	4 0.1×	50	405
Lucia Perone Italy	12	198 1.1×	217 1.6×	10 0.2×	19 0.4×	12 0.2×	21	361
Bobo Xie China	13	178 1.0×	106 0.8×	9 0.1×	14 0.3×	3 0.1×	38	366
Faouzi Mâazoul Tunisia	13	424 2.4×	345 2.6×	5 0.1×	30 0.6×	7 0.1×	46	567
Caleb Bupp United States	13	251 1.4×	164 1.2×	8 0.1×	18 0.3×	10 0.2×	43	424
Massimiliano Cocca Italy	9	91 0.5×	92 0.7×	96 1.5×	78 1.4×	26 0.5×	20	352

Countries citing papers authored by Kent E. Kruckeberg

Since Specialization

Citations

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

Fields of papers citing papers by Kent E. Kruckeberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kent E. Kruckeberg. 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 Kent E. Kruckeberg. The network helps show where Kent E. Kruckeberg may publish in the future.

Co-authorship network of co-authors of Kent E. Kruckeberg

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

All Works

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9 of 9 papers shown

Baudhuin, Linnea M., Ming Mai, Amy J. French, et al.. (2005). Analysis of hMLH1 and hMSH2 Gene Dosage Alterations in Hereditary Nonpolyposis Colorectal Cancer Patients by Novel Methods. Journal of Molecular Diagnostics. 7(2). 226–235. 21 indexed citations

Cradic, Kendall W, et al.. (2004). Substitution of 3′-Phosphate Cap with a Carbon-Based Blocker Reduces the Possibility of Fluorescence Resonance Energy Transfer Probe Failure in Real-Time PCR Assays. Clinical Chemistry. 50(6). 1080–1082. 15 indexed citations

Kruckeberg, Kent E. & Stephen N. Thibodeau. (2004). Pyrosequencing Technology as a Method for the Diagnosis of Multiple Endocrine Neoplasia Type 2. Clinical Chemistry. 50(3). 522–529. 12 indexed citations

Nagan, Narasimhan, et al.. (2003). The frequency of short-chain acyl-CoA dehydrogenase gene variants in the US population and correlation with the C4-acylcarnitine concentration in newborn blood spots. Molecular Genetics and Metabolism. 78(4). 239–246. 52 indexed citations

Brandhagen, David J., Virgil F. Fairbanks, W P Baldus, et al.. (2000). Prevalence and Clinical Significance of Hfe Gene Mutations in Patients With Iron Overload. The American Journal of Gastroenterology. 95(10). 2910–2914. 16 indexed citations

Nguyen, Tu T., Kent E. Kruckeberg, John F. O’Brien, et al.. (2000). Familial Splenomegaly: Macrophage Hypercatabolism of Lipoproteins Associated with Apolipoprotein E Mutation [Apolipoprotein E (Δ149 Leu)]. The Journal of Clinical Endocrinology & Metabolism. 85(11). 4354–4358. 25 indexed citations

Brandhagen, David J., William Alvarez, Terry M. Therneau, et al.. (2000). Iron overload in cirrhosis— HFE genotypes and outcome after liver transplantation. Hepatology. 31(2). 456–460. 64 indexed citations

Snow, K., et al.. (1994). Sequence analysis of the fragile X trinucleotide repeat: Correlations with stability and haplotype and implications for the origin of fragile X alleles. The American Journal of Human Genetics. 55. 1 indexed citations

Snow, Karen, David J. Tester, Kent E. Kruckeberg, Daniel J. Schaid, & Stephen N. Thibodeau. (1994). Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation. Human Molecular Genetics. 3(9). 1543–1551. 144 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.

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