Steven D. Klein

997 total citations
31 papers, 677 citations indexed

About

Steven D. Klein is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Steven D. Klein has authored 31 papers receiving a total of 677 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 14 papers in Genetics and 11 papers in Surgery. Recurrent topics in Steven D. Klein's work include Genetic Syndromes and Imprinting (5 papers), Epigenetics and DNA Methylation (4 papers) and Renal and related cancers (4 papers). Steven D. Klein is often cited by papers focused on Genetic Syndromes and Imprinting (5 papers), Epigenetics and DNA Methylation (4 papers) and Renal and related cancers (4 papers). Steven D. Klein collaborates with scholars based in United States, Germany and Australia. Steven D. Klein's co-authors include Julián A. Martínez-Agosto, John Affronti, R. D. Soloway, Johannes A. Romijn, Yoshinori Sakurai, R. M. Carroll, Shahnaz Ghahremani, Stanley F. Nelson, Hane Lee and Éric Vilain and has published in prestigious journals such as Gastroenterology, American Journal of Clinical Nutrition and Annals of Neurology.

In The Last Decade

Steven D. Klein

28 papers receiving 654 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Steven D. Klein United States 15 239 221 145 121 112 31 677
Sonia Salisbury Canada 15 85 0.4× 217 1.0× 169 1.2× 47 0.4× 61 0.5× 22 670
Patrick Rump Netherlands 21 69 0.3× 547 2.5× 487 3.4× 77 0.6× 89 0.8× 39 1.2k
Rivka Kauli Israel 22 116 0.5× 451 2.0× 316 2.2× 46 0.4× 106 0.9× 70 1.3k
David Kronn United States 15 72 0.3× 362 1.6× 270 1.9× 79 0.7× 195 1.7× 35 1.0k
Erica Penman United Kingdom 16 279 1.2× 296 1.3× 42 0.3× 53 0.4× 68 0.6× 24 811
Salvador Castells United States 17 138 0.6× 153 0.7× 380 2.6× 21 0.2× 78 0.7× 51 813
Rachel E. Weitzman United States 13 249 1.0× 125 0.6× 53 0.4× 49 0.4× 114 1.0× 35 763
Masaki Miura Japan 16 169 0.7× 163 0.7× 66 0.5× 60 0.5× 56 0.5× 56 649
Oliver Quarrell United Kingdom 17 57 0.2× 369 1.7× 237 1.6× 39 0.3× 22 0.2× 44 862
Hitoshi Fujioka Japan 15 157 0.7× 93 0.4× 53 0.4× 65 0.5× 93 0.8× 43 646

Countries citing papers authored by Steven D. Klein

Since Specialization
Citations

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

Fields of papers citing papers by Steven D. Klein

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Steven D. Klein. 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 Steven D. Klein. The network helps show where Steven D. Klein may publish in the future.

Co-authorship network of co-authors of Steven D. Klein

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

All Works

20 of 20 papers shown
1.
Arias, Pedro, Steven D. Klein, Julián Nevado, et al.. (2024). Phenotypic spectrum and tumor risk in Simpson‐Golabi‐Behmel syndrome: Case series and comprehensive literature review. American Journal of Medical Genetics Part A. 194(12). e63840–e63840. 4 indexed citations
2.
Kalish, Jennifer M., Gaëlle Bougeard, Garrett M. Brodeur, et al.. (2024). Update on Surveillance for Wilms Tumor and Hepatoblastoma in Beckwith–Wiedemann Syndrome and Other Predisposition Syndromes. Clinical Cancer Research. 30(23). 5260–5269. 9 indexed citations
3.
Klein, Steven D., et al.. (2023). Occurrence of Hepatoblastomas in Patients with Beckwith–Wiedemann Spectrum (BWSp). Cancers. 15(9). 2548–2548. 5 indexed citations
4.
Mullegama, Sureni V., Steven D. Klein, Stephen R. Williams, et al.. (2021). Transcriptome analysis of MBD5-associated neurodevelopmental disorder (MAND) neural progenitor cells reveals dysregulation of autism-associated genes. Scientific Reports. 11(1). 11295–11295. 6 indexed citations
5.
Duffy, Kelly A., et al.. (2021). Epigenetic mosaicism and cell burden in Beckwith–Wiedemann syndrome due to loss of methylation at imprinting control region 2. Molecular Case Studies. 7(6). a006115–a006115. 13 indexed citations
6.
7.
Mullegama, Sureni V., Steven D. Klein, Rebecca Signer, Éric Vilain, & Julián A. Martínez-Agosto. (2018). Mutations in STAG2 cause an X‐linked cohesinopathy associated with undergrowth, developmental delay, and dysmorphia: Expanding the phenotype in males. Molecular Genetics & Genomic Medicine. 7(2). e00501–e00501. 28 indexed citations
8.
Mullegama, Sureni V., Steven D. Klein, T. Niroshini Senaratne, et al.. (2017). De novo loss‐of‐function variants in STAG2 are associated with developmental delay, microcephaly, and congenital anomalies. American Journal of Medical Genetics Part A. 173(5). 1319–1327. 36 indexed citations
9.
Bramble, Matthew S., Allen Lipson, Ascia Eskin, et al.. (2016). Sex-Specific Effects of Testosterone on the Sexually Dimorphic Transcriptome and Epigenome of Embryonic Neural Stem/Progenitor Cells. Scientific Reports. 6(1). 36916–36916. 33 indexed citations
10.
Klein, Steven D., Alexander Goldman, Hane Lee, et al.. (2016). Truncating mutations in APP cause a distinct neurological phenotype. Annals of Neurology. 80(3). 456–460. 18 indexed citations
11.
Klein, Steven D., et al.. (2013). Macrocephaly as a Clinical Indicator of Genetic Subtypes in Autism. Autism Research. 6(1). 51–56. 72 indexed citations
12.
Klein, Steven D., et al.. (2012). Phenotypic progression of skeletal anomalies in CLOVES syndrome. American Journal of Medical Genetics Part A. 158A(7). 1690–1695. 15 indexed citations
13.
Danzi, Sara, Steven D. Klein, & Irwin Klein. (2008). Differential Regulation of the Myosin Heavy Chain Genes α and β in Rat Atria and Ventricles: Role of Antisense RNA. Thyroid. 18(7). 761–768. 20 indexed citations
14.
Klein, Steven D., et al.. (2006). Endoscopic Retrograde Cholangiopancreatography after a Liquid Fatty Meal: Effect on Deep Common Bile Duct Cannulation Time. Endoscopy. 38(3). 241–248. 4 indexed citations
15.
Klein, Steven D. & John Affronti. (2004). Pancreas divisum, an evidence-based review: part I, pathophysiology. Gastrointestinal Endoscopy. 60(3). 419–425. 63 indexed citations
16.
Klein, Steven D. & John Affronti. (2004). Pancreas divisum, an evidence-based review: part II, patient selection and treatment. Gastrointestinal Endoscopy. 60(4). 585–589. 27 indexed citations
17.
Klein, Steven D., Laura S. Hamilton, Daniel F. McCaffrey, & Brian M. Stecher. (2000). ISSUE PAPER: What Do Test Scores in Texas Tell Us?. Defense Technical Information Center (DTIC). 2 indexed citations
18.
Carroll, R. M. & Steven D. Klein. (1995). Effect of energy compared with carbohydrate restriction on the lipolytic response to epinephrine. American Journal of Clinical Nutrition. 62(4). 757–760. 1 indexed citations
19.
Klein, Steven D., et al.. (1992). [Cyclosporin A in therapy of chronic uveitis].. PubMed. 89(5). 411–5. 2 indexed citations
20.
Klein, Steven D., et al.. (1973). Panel discussion on surgical management of inflammatory bowel disease.. PubMed. 60(3). 213–39.

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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