Michael Kennemer

1.5k total citations
4 papers, 181 citations indexed

About

Michael Kennemer is a scholar working on Molecular Biology, Genetics and Organic Chemistry. According to data from OpenAlex, Michael Kennemer has authored 4 papers receiving a total of 181 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Organic Chemistry. Recurrent topics in Michael Kennemer's work include Genomic variations and chromosomal abnormalities (2 papers), RNA modifications and cancer (1 paper) and Cancer Genomics and Diagnostics (1 paper). Michael Kennemer is often cited by papers focused on Genomic variations and chromosomal abnormalities (2 papers), RNA modifications and cancer (1 paper) and Cancer Genomics and Diagnostics (1 paper). Michael Kennemer collaborates with scholars based in United States and Israel. Michael Kennemer's co-authors include Rebecca Truty, Robert L. Nussbaum, Swaroop Aradhya, Eric C. Olivares, Joshua Paul, Stephen E. Lincoln, Steven J. Pitts, Gary E. Swan, Renee Stokowski and David A. Hinds and has published in prestigious journals such as The American Journal of Human Genetics, Neuropsychopharmacology and Genetics in Medicine.

In The Last Decade

Michael Kennemer

4 papers receiving 180 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Michael Kennemer United States	4	92	92	26	25	23	4	181
Julie A. Jurgens United States	11	148 1.6×	124 1.3×	25 1.0×	23 0.9×	10 0.4×	14	298
Haktan Bağış Erdem Türkiye	9	68 0.7×	53 0.6×	19 0.7×	11 0.4×	13 0.6×	34	161
Yaser Heshmati Sweden	9	103 1.1×	36 0.4×	30 1.2×	17 0.7×	23 1.0×	15	201
Agostino Seresini Italy	6	96 1.0×	35 0.4×	28 1.1×	16 0.6×	17 0.7×	8	160
Arthur Sorlin France	8	115 1.3×	86 0.9×	18 0.7×	13 0.5×	6 0.3×	23	224
Minal Menezes Australia	10	195 2.1×	65 0.7×	27 1.0×	16 0.6×	9 0.4×	17	290
Gabrielle Lemire Canada	7	91 1.0×	72 0.8×	12 0.5×	16 0.6×	9 0.4×	16	165
A. Saad Tunisia	9	97 1.1×	130 1.4×	13 0.5×	26 1.0×	24 1.0×	24	255
Ewa Goljan Saudi Arabia	7	90 1.0×	81 0.9×	11 0.4×	11 0.4×	19 0.8×	9	218
Taghreed Shuaib Saudi Arabia	9	133 1.4×	74 0.8×	19 0.7×	18 0.7×	10 0.4×	13	243

Countries citing papers authored by Michael Kennemer

Since Specialization

Citations

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

Fields of papers citing papers by Michael Kennemer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael Kennemer

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

All Works

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4 of 4 papers shown

1.

Truty, Rebecca, Susan Rojahn, Karen Ouyang, et al.. (2023). Patterns of mosaicism for sequence and copy-number variants discovered through clinical deep sequencing of disease-related genes in one million individuals. The American Journal of Human Genetics. 110(4). 551–564. 8 indexed citations

2.

Tan, Christopher, M. Jody Westbrook, Rebecca Truty, et al.. (2020). Incorporating Spinal Muscular Atrophy Analysis by Next-Generation Sequencing into a Comprehensive Multigene Panel for Neuromuscular Disorders. Genetic Testing and Molecular Biomarkers. 24(10). 616–624. 11 indexed citations

3.

Truty, Rebecca, Joshua Paul, Michael Kennemer, et al.. (2018). Prevalence and properties of intragenic copy-number variation in Mendelian disease genes. Genetics in Medicine. 21(1). 114–123. 114 indexed citations

4.

Wessel, Jennifer, Sarah M. McDonald, David A. Hinds, et al.. (2010). Resequencing of Nicotinic Acetylcholine Receptor Genes and Association of Common and Rare Variants with the Fagerström Test for Nicotine Dependence. Neuropsychopharmacology. 35(12). 2392–2402. 48 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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