B Kattman

8.4k total citations
25 papers, 676 citations indexed

About

B Kattman is a scholar working on Genetics, Molecular Biology and Pharmacology. According to data from OpenAlex, B Kattman has authored 25 papers receiving a total of 676 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Pharmacology. Recurrent topics in B Kattman's work include Genomics and Rare Diseases (8 papers), Pharmacogenetics and Drug Metabolism (5 papers) and Cancer Genomics and Diagnostics (4 papers). B Kattman is often cited by papers focused on Genomics and Rare Diseases (8 papers), Pharmacogenetics and Drug Metabolism (5 papers) and Cancer Genomics and Diagnostics (4 papers). B Kattman collaborates with scholars based in United States and United Kingdom. B Kattman's co-authors include Melissa Landrum, Adriana Malheiro, Victoria M. Pratt, Bernard Esquivel, Megan Kane, Stuart A. Scott, Munir Pirmohamed, J. Bradley Holmes, Lon Phan and Alejandro A. Schäffer and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Oncology and Bioinformatics.

In The Last Decade

B Kattman

22 papers receiving 666 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
B Kattman United States	9	207	179	126	82	77	25	676
Megan Kane United States	11	259 1.3×	98 0.5×	114 0.9×	85 1.0×	69 0.9×	28	660
Roslan Harun Malaysia	16	232 1.1×	73 0.4×	68 0.5×	163 2.0×	90 1.2×	36	678
Christodoulos Flordellis Greece	17	368 1.8×	78 0.4×	95 0.8×	74 0.9×	56 0.7×	45	883
Marilu Fiegenbaum Brazil	17	176 0.9×	187 1.0×	108 0.9×	98 1.2×	48 0.6×	61	891
K. I. Pritchard Canada	8	75 0.4×	219 1.2×	96 0.8×	247 3.0×	52 0.7×	25	563
Evgeny Krynetskiy United States	16	245 1.2×	70 0.4×	69 0.5×	83 1.0×	37 0.5×	36	729
Marcelo R. Luizon Brazil	23	291 1.4×	115 0.6×	89 0.7×	64 0.8×	271 3.5×	86	1.3k
Charlotte Brasch‐Andersen Denmark	19	497 2.4×	198 1.1×	177 1.4×	302 3.7×	124 1.6×	49	1.1k
Santosh Philips United States	15	169 0.8×	217 1.2×	139 1.1×	171 2.1×	56 0.7×	40	574
Christian Hengstenberg Germany	20	367 1.8×	173 1.0×	46 0.4×	38 0.5×	45 0.6×	37	1.1k

Countries citing papers authored by B Kattman

Since Specialization

Citations

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

Fields of papers citing papers by B Kattman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B Kattman

This figure shows the co-authorship network connecting the top 25 collaborators of B Kattman. A scholar is included among the top collaborators of B Kattman 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 B Kattman. B Kattman 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

Malheiro, Adriana, Megan Kane, Douglas Hoffman, et al.. (2025). P306: MedGen: An integrated and comprehensive resource for medical genetics concepts and concept-associated information. Genetics in Medicine Open. 3. 102271–102271. 1 indexed citations

Ward, Minghong, J. S. Bloom, Mike Feolo, et al.. (2025). P604: Advancing genomic research: Enhancing dbGaP interoperability with FHIR APIs. Genetics in Medicine Open. 3. 102452–102452.

Phan, Lon, et al.. (2024). The evolution of dbSNP: 25 years of impact in genomic research. Nucleic Acids Research. 53(D1). D925–D931. 26 indexed citations

Landrum, Melissa, Shanmuga Chitipiralla, Kuljeet Kaur, et al.. (2024). ClinVar: updates to support classifications of both germline and somatic variants. Nucleic Acids Research. 53(D1). D1313–D1321. 22 indexed citations

Pratt, Victoria M., Stuart A. Scott, Munir Pirmohamed, et al.. (2021). Codeine Therapy and CYP2D6 Genotype.

Malheiro, Adriana, Baoshan Gu, Chao Chen, et al.. (2020). How the NIH Genetic Testing Registry and Medical Genetics Summaries can help oncologists adopt pharmacogenetics guidelines.. Journal of Clinical Oncology. 38(15_suppl). e14141–e14141.

Holmes, J. Bradley, et al.. (2019). SPDI: data model for variants and applications at NCBI. Bioinformatics. 36(6). 1902–1907. 26 indexed citations

Jin, Yumi, Alejandro A. Schäffer, Michael Feolo, J. Bradley Holmes, & B Kattman. (2019). GRAF-pop: A Fast Distance-Based Method To Infer Subject Ancestry from Multiple Genotype Datasets Without Principal Components Analysis. G3 Genes Genomes Genetics. 9(8). 2447–2461. 33 indexed citations

Azzariti, Danielle R., Erin Rooney Riggs, Annie Niehaus, et al.. (2018). Points to consider for sharing variant-level information from clinical genetic testing with ClinVar. Molecular Case Studies. 4(1). a002345–a002345. 16 indexed citations

10.

Landrum, Melissa & B Kattman. (2018). ClinVar at five years: Delivering on the promise. Human Mutation. 39(11). 1623–1630. 120 indexed citations

11.

Savatt, Juliann M., Danielle R. Azzariti, W. Andrew Faucett, et al.. (2018). ClinGen's GenomeConnect registry enables patient‐centered data sharing. Human Mutation. 39(11). 1668–1676. 24 indexed citations

12.

Rubinstein, Wendy S., Adriana Malheiro, B Kattman, et al.. (2016). Landscape scanning of cancer gene panels: A report from the NIH Genetic Testing Registry (GTR).. Journal of Clinical Oncology. 34(15_suppl). e13120–e13120. 1 indexed citations

13.

McLeod, H. L., et al.. (2012). Atomoxetine Therapy and CYP2D6 Genotype -- Medical Genetics Summaries. 3 indexed citations

14.

McLeod, H. L., et al.. (2012). Metoprolol Therapy and CYP2D6 Genotype -- Medical Genetics Summaries. 2 indexed citations

15.

McLeod, H. L., et al.. (2012). Azathioprine Therapy and TPMT Genotype -- Medical Genetics Summaries. 4 indexed citations

16.

McLeod, H. L., et al.. (2012). Flurbiprofen Therapy and CYP2C9 Genotype -- Medical Genetics Summaries. 1 indexed citations

17.

McLeod, H. L., et al.. (2012). Carisoprodol Therapy and CYP2C19 Genotype -- Medical Genetics Summaries. 2 indexed citations

18.

McLeod, H. L., et al.. (2012). Irinotecan Therapy and UGT1A1 Genotype -- Medical Genetics Summaries. 2 indexed citations

19.

McLeod, H. L., et al.. (2012). Celecoxib Therapy and CYP2C9 Genotype -- Medical Genetics Summaries. 1 indexed citations

20.

McLeod, H. L., et al.. (2012). Deutetrabenazine Therapy and CYP2D6 Genotype -- Medical Genetics Summaries. 3 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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