Michael D. Graf

937 total citations
11 papers, 186 citations indexed

About

Michael D. Graf is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Michael D. Graf has authored 11 papers receiving a total of 186 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Pediatrics, Perinatology and Child Health and 3 papers in Molecular Biology. Recurrent topics in Michael D. Graf's work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and T-cell and Retrovirus Studies (2 papers). Michael D. Graf is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and T-cell and Retrovirus Studies (2 papers). Michael D. Graf collaborates with scholars based in United States, Germany and Netherlands. Michael D. Graf's co-authors include Stuart Schwartz, David J. Driscoll, Eric Libby, Steven Jacobson, Allen Waziri, Samantha S. Soldan, Ayse Anil Timur, Qing K. Wang, Taketo Kawanishi and Tanya Lehky and has published in prestigious journals such as Journal of Virology, The Journal of Infectious Diseases and Journal of Medical Genetics.

In The Last Decade

Michael D. Graf

11 papers receiving 176 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Michael D. Graf United States	7	84	52	39	39	38	11	186
Teena Koshy India	9	61 0.7×	30 0.6×	16 0.4×	74 1.9×	29 0.8×	41	250
Jianchi Ding United States	11	88 1.0×	27 0.5×	29 0.7×	96 2.5×	160 4.2×	20	570
Benjamin R. Sessions United States	13	76 0.9×	43 0.8×	11 0.3×	176 4.5×	33 0.9×	31	325
Yung‐Tsi Bolon United States	10	28 0.3×	9 0.2×	16 0.4×	48 1.2×	95 2.5×	36	306
Jiadi Wen United States	9	124 1.5×	125 2.4×	16 0.4×	84 2.2×	57 1.5×	22	264
Ken Dowell United Kingdom	13	98 1.2×	246 4.7×	16 0.4×	61 1.6×	61 1.6×	21	572
Kaifeng Wu China	7	58 0.7×	18 0.3×	8 0.2×	76 1.9×	4 0.1×	13	164
T.K. Yoon South Korea	10	71 0.8×	56 1.1×	15 0.4×	155 4.0×	74 1.9×	22	413
Caroline Eozénou France	12	159 1.9×	16 0.3×	11 0.3×	149 3.8×	94 2.5×	17	329

Countries citing papers authored by Michael D. Graf

Since Specialization

Citations

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

Fields of papers citing papers by Michael D. Graf

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael D. Graf

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

All Works

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11 of 11 papers shown

Graf, Michael D., Luiz Olavo Bonino da Silva Santos, Stefan Decker, et al.. (2024). A study on interoperability between two Personal Health Train infrastructures in leukodystrophy data analysis. Scientific Data. 11(1). 663–663. 3 indexed citations

Graf, Michael D., et al.. (2013). Genetic Testing Insurance Coverage Trends: A Review of Publicly Available Policies from the Largest us Payers. Personalized Medicine. 10(3). 235–243. 41 indexed citations

Harris, Heather A., et al.. (2011). Analysis of Insurance Preauthorization Requests for BRCA1 and BRCA2 Genetic Testing: Experience of the Humana Genetic Guidance Program. Personalized Medicine. 8(5). 563–569. 1 indexed citations

Graf, Michael D., et al.. (2006). Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study. Journal of Medical Genetics. 43(8). 660–664. 39 indexed citations

Timur, Ayse Anil, Michael D. Graf, Stuart Schwartz, et al.. (2004). Identification and Molecular Characterization of a de novo Supernumerary Ring Chromosome 18 in a Patient with Klippel‐Trenaunay Syndrome. Annals of Human Genetics. 68(4). 353–361. 40 indexed citations

Schwartz, Stuart & Michael D. Graf. (2003). Microdeletion Syndromes: Characteristics and Diagnosis. Molecular Cytogenetics. 204. 275–290. 4 indexed citations

Graf, Michael D. & Stuart Schwartz. (2003). Molecular Approaches for Delineating Marker Chromosomes. Molecular Cytogenetics. 204. 211–218. 2 indexed citations

Graf, Michael D., et al.. (2002). Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screening. Prenatal Diagnosis. 22(8). 645–648. 7 indexed citations

Waziri, Allen, et al.. (2000). Characterization and Sequencing of Prototypic Human T-Lymphotropic Virus Type 1 (HTLV-1) from an HTLV-1/2 Seroindeterminate Patient. Journal of Virology. 74(5). 2178–2185. 20 indexed citations

10.

Soldan, Samantha S., Michael D. Graf, Allen Waziri, et al.. (1999). HTLV‐I/II Seroindeterminate Western Blot Reactivity in a Cohort of Patients with Neurological Disease. The Journal of Infectious Diseases. 180(3). 685–694. 15 indexed citations

11.

Sorgo, W., Ludwig Gortner, Peter Bartmann, et al.. (1991). Gonadal Agenesis in a 46, XY Female with Multiple Malformations and Positive Testing for the Sex-Determining Region of the Y Chromosome. Hormone Research. 35(3-4). 124–131. 14 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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