Michael E. Talkowski

39.0k total citations · 1 hit paper
100 papers, 4.3k citations indexed

About

Michael E. Talkowski is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Michael E. Talkowski has authored 100 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Genetics, 60 papers in Molecular Biology and 13 papers in Cellular and Molecular Neuroscience. Recurrent topics in Michael E. Talkowski's work include Genomic variations and chromosomal abnormalities (33 papers), Genomics and Rare Diseases (23 papers) and Genetics and Neurodevelopmental Disorders (19 papers). Michael E. Talkowski is often cited by papers focused on Genomic variations and chromosomal abnormalities (33 papers), Genomics and Rare Diseases (23 papers) and Genetics and Neurodevelopmental Disorders (19 papers). Michael E. Talkowski collaborates with scholars based in United States, United Kingdom and Italy. Michael E. Talkowski's co-authors include James F. Gusella, Harrison Brand, Serkan Erdin, Ryan L. Collins, Ashok Ragavendran, Kiran Musunuru, Chad A. Cowan, Vishwajit L. Nimgaonkar, Kodavali V. Chowdari and Alexei Stortchevoi and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Michael E. Talkowski

98 papers receiving 4.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Efficient Ablation of Genes in Human Hematopoietic Stem and Effector Cells using CRISPR/Cas9

2014 379 citations Ryan L. Collins, Alexei Stortchevoi et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Michael E. Talkowski United States	32	2.7k	1.9k	489	324	323	100	4.3k
Yann Hérault France	38	3.0k 1.1×	1.8k 1.0×	364 0.7×	288 0.9×	221 0.7×	158	5.8k
Nicoletta Landsberger Italy	30	4.4k 1.6×	2.9k 1.5×	762 1.6×	275 0.8×	278 0.9×	73	5.6k
Jennifer L. Moran United States	33	2.7k 1.0×	2.3k 1.2×	325 0.7×	330 1.0×	264 0.8×	62	4.7k
Tjitske Kleefstra Netherlands	38	3.4k 1.3×	3.7k 2.0×	696 1.4×	483 1.5×	239 0.7×	131	5.7k
Hilde Van Esch Belgium	40	3.5k 1.3×	3.5k 1.8×	682 1.4×	338 1.0×	250 0.8×	148	5.6k
Vera M. Kalscheuer Germany	45	4.4k 1.6×	3.6k 1.9×	407 0.8×	586 1.8×	351 1.1×	152	6.7k
Thierry Bienvenu France	38	2.4k 0.9×	3.2k 1.7×	944 1.9×	379 1.2×	133 0.4×	200	5.6k
Montserrat Milà Spain	34	2.2k 0.8×	1.8k 1.0×	934 1.9×	511 1.6×	199 0.6×	140	4.0k
Fiona Francis France	39	2.9k 1.1×	1.8k 0.9×	336 0.7×	1.2k 3.7×	284 0.9×	103	6.5k

Countries citing papers authored by Michael E. Talkowski

Since Specialization

Citations

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

Fields of papers citing papers by Michael E. Talkowski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael E. Talkowski

This figure shows the co-authorship network connecting the top 25 collaborators of Michael E. Talkowski. A scholar is included among the top collaborators of Michael E. Talkowski 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 E. Talkowski. Michael E. Talkowski 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

Reeve, Mary Pat, Stephanie Loomis, Eija Nissilä, et al.. (2025). Loss of CFHR5 function reduces the risk for age-related macular degeneration. Nature Communications. 16(1). 5766–5766. 1 indexed citations

Li, Haobo, Serkan Erdin, Matthew J. Smith, et al.. (2025). Whole-blood transcriptomic analysis reveals preoperative complement inhibitor deficiencies linked to postoperative delirium. Molecular Psychiatry. 30(10). 4690–4699.

Mahmoud, Medhat, Yongqing Huang, Kiran Garimella, et al.. (2024). Utility of long-read sequencing for All of Us. Nature Communications. 15(1). 837–837. 43 indexed citations

Duyzend, Michael, Pilar Cacheiro, Julius O.B. Jacobsen, et al.. (2024). Improving prenatal diagnosis through standards and aggregation. Prenatal Diagnosis. 44(4). 454–464. 3 indexed citations

Babadi, Mehrtash, Jack Fu, Samuel K. Lee, et al.. (2023). GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data. Nature Genetics. 55(9). 1589–1597. 35 indexed citations

Pérez‐Palma, Eduardo, Tobias Brünger, Konrad Platzer, et al.. (2023). CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants online. Bioinformatics. 39(5). 8 indexed citations

Wahlster, Lara, Jeffrey M. Verboon, Leif S. Ludwig, et al.. (2021). Familial thrombocytopenia due to a complex structural variant resulting in a WAC-ANKRD26 fusion transcript. The Journal of Experimental Medicine. 218(6). 10 indexed citations

Rodriguez, Steven, Benjamin R. Schrank, Isabel Costantino, et al.. (2021). Genome-encoded cytoplasmic double-stranded RNAs, found in C9ORF72 ALS-FTD brain, propagate neuronal loss. Science Translational Medicine. 13(601). 29 indexed citations

Morini, Elisabetta, Dadi Gao, Monica Salani, et al.. (2021). Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage. Journal of genetics and genomics. 49(7). 654–665. 6 indexed citations

10.

Kousi, Maria, Onuralp Söylemez, Niki Mourtzi, et al.. (2020). Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy. Nature Genetics. 52(11). 1145–1150. 21 indexed citations

11.

Kovalenko, Marina, Serkan Erdin, Jason St. Claire, et al.. (2020). Histone deacetylase knockouts modify transcription, CAG instability and nuclear pathology in Huntington disease mice. eLife. 9. 8 indexed citations

12.

Stamou, Maria, Shi‐Yan Ng, Harrison Brand, et al.. (2019). A Balanced Translocation in Kallmann Syndrome Implicates a Long Noncoding RNA, RMST, as a GnRH Neuronal Regulator. The Journal of Clinical Endocrinology & Metabolism. 105(3). e231–e244. 23 indexed citations

13.

Tebaldi, Toma, Toshimi Yoshida, Serkan Erdin, et al.. (2019). Hypomorphic mutation of the mouse Huntington’s disease gene orthologue. PLoS Genetics. 15(3). e1007765–e1007765. 13 indexed citations

14.

Boone, Philip M., Scott Paterson, Kiana Mohajeri, et al.. (2019). Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome. American Journal of Medical Genetics Part A. 182(1). 189–194. 12 indexed citations

15.

Morini, Elisabetta, Dadi Gao, Monica Salani, et al.. (2019). ELP1 Splicing Correction Reverses Proprioceptive Sensory Loss in Familial Dysautonomia. The American Journal of Human Genetics. 104(4). 638–650. 26 indexed citations

16.

Roosmalen, Markus J. van, Ivo Renkens, Marleen M. Nieboer, et al.. (2017). Mapping and phasing of structural variation in patient genomes using nanopore sequencing. Nature Communications. 8(1). 1326–1326. 249 indexed citations

17.

Seabra, Catarina M., Serkan Erdin, Ashok Ragavendran, et al.. (2017). A novel microduplication of ARID1B: Clinical, genetic, and proteomic findings. American Journal of Medical Genetics Part A. 173(9). 2478–2484. 5 indexed citations

18.

Talkowski, Michael E., Carl Ernst, Adrian Heilbut, et al.. (2011). Next-Generation Sequencing Strategies Enable Routine Detection of Balanced Chromosome Rearrangements for Clinical Diagnostics and Genetic Research. The American Journal of Human Genetics. 88(4). 469–481. 120 indexed citations

19.

Prasad, Konasale M., Kodavali V. Chowdari, Vishwajit L. Nimgaonkar, et al.. (2004). Genetic polymorphisms of the RGS4 and dorsolateral prefrontal cortex morphometry among first episode schizophrenia patients. Molecular Psychiatry. 10(2). 213–219. 83 indexed citations

20.

Redfern, Mark S., Michael E. Talkowski, J. Richard Jennings, & Joseph M. Furman. (2003). Cognitive influences in postural control of patients with unilateral vestibular loss. Gait & Posture. 19(2). 105–114. 112 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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