Michael E. Talkowski

39.0k citations
100 papers · 4.3k · 1 hit paper · h-index 32

Impact in

  • Aging top 2%
  • Genetics top 0.5%
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases

Papers in

  • Genetics 66
    • Genomic variations and chromosomal abnormalities 33
    • Genomics and Rare Diseases 23
    • Genetics and Neurodevelopmental Disorders 19
    • Genetic Associations and Epidemiology 11
  • Molecular Biology 60
    • CRISPR and Genetic Engineering 13
    • Congenital heart defects research 11
Co-authors
James F. Gusella (27 shared papers)Harrison Brand (16 shared papers)Serkan Erdin (24 shared papers)Ryan L. Collins (16 shared papers)Ashok Ragavendran (9 shared papers)Kiran Musunuru (3 shared papers)Chad A. Cowan (3 shared papers)Vishwajit L. Nimgaonkar (12 shared papers)
Journals
The American Journal of Human Genetics (10 papers)Schizophrenia Bulletin (6 papers)European Neuropsychopharmacology (6 papers)Nature Communications (5 papers)Human Molecular Genetics (4 papers)
Partner nations
United StatesUnited KingdomItaly

In The Last Decade

Michael E. Talkowski

98 papers receiving 4.2k citations

Michael E. Talkowski's Hit Papers

Efficient Ablation of Genes in Human Hematopoietic Stem and Effector Cells using CRISPR/Cas9 2014 · 379 citations
3790+4+8Years since publication100200300
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

  • it has ≥500 total citations;
  • it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
  • it reaches the top citation threshold in at least one of its specific research topics.
  1. 2014 Cell stem cell

Peers

Michael E. Talkowski
Comparison fields: 5 of 136
  • Aging 135
  • Genetics 1.9k
  • Business and International Management 123
  • Molecular Biology 2.7k
  • Biological Psychiatry 65
Replace Kathleen A. Worringer with:
Kathleen A. Worringer United States
Zilong Qiu China
Zhaolan Zhou United States
Yann Hérault France
In‐Hyun Park United States
Matthias Heidenreich United States
Kristen Brennand United States
Luciano Conti Italy
Hiroaki Mizukami Japan
Michael E. Talkowski relative to Kathleen A. Worringer United States Kathleen A. Worringer's profile →
Citations per field
00.5×2×3×4.3×
Kathleen A. Worringer · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Michael E. Talkowski, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Michael E. Talkowski Line = papers co-authored together Michael E. Talkowski links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 100 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Efficient Ablation of Genes in Human Hematopoietic Stem and Effector Cells using CRISPR/Cas9
Cell stem cell ·Pankaj Kumar Mandal, Leonardo M. R. Ferreira, Ryan L. Collins, Torsten Meißner, Christian L. Boutwell, Max Friesen, Vladimir Vrbanac, Brian S. Garrison, Alexei Stortchevoi, David Bryder, Kiran Musunuru, Harrison Brand, Andrew M. Tager, Todd M. Allen, Michael E. Talkowski, Derrick J. Rossi, Chad A. Cowan
Hit paper breakdown →		2014379
2
Low Incidence of Off-Target Mutations in Individual CRISPR-Cas9 and TALEN Targeted Human Stem Cell Clones Detected by Whole-Genome Sequencing
Cell stem cell ·Adrian Veres, Bridget S. Gosis, Qiurong Ding, Ryan L. Collins, Ashok Ragavendran, Harrison Brand, Serkan Erdin, Chad A. Cowan, Michael E. Talkowski, Kiran Musunuru
2014378
3
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant
Nature ·Christelle Golzio, Jason R. Willer, Michael E. Talkowski, Edwin C. Oh, Yu Taniguchi, Sébastien Jacquemont, Alexandre Reymond, Mei Sun, Akira Sawa, James F. Gusella, Atsushi Kamiya, J. Beckmann, Nicholas Katsanis
2012264
4
Mapping and phasing of structural variation in patient genomes using nanopore sequencing
Nature Communications ·Mircea Cretu Stancu, Markus J. van Roosmalen, Ivo Renkens, Marleen M. Nieboer, Sjors Middelkamp, Joep de Ligt, Giulia Pregno, Daniela Giachino, Giorgia Mandrile, Jose Espejo Valle-Inclán, Jerome Korzelius, Ewart de Bruijn, Edwin Cuppen, Michael E. Talkowski, Tobias Marschall, Jeroen de Ridder, Wigard P. Kloosterman
2017249
5
Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations
Nature ·Po‐Ru Loh, Giulio Genovese, Robert E. Handsaker, Hilary K. Finucane, Yakir Reshef, Pier Francesco Palamara, Brenda M. Birmann, Michael E. Talkowski, Samuel F. Bakhoum, Steven A. McCarroll, Alkes L. Price
2018229
6
CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors
Proceedings of the National Academy of Sciences ·Aarathi Sugathan, Marta Biagioli, Christelle Golzio, Serkan Erdin, Ian Blumenthal, Poornima Manavalan, Ashok Ragavendran, Harrison Brand, Diane Lucente, Judith H. Miles, Steven D. Sheridan, Alexei Stortchevoi, Manolis Kellis, Stephen J. Haggarty, Nicholas Katsanis, James F. Gusella, Michael E. Talkowski
2014227
7
An Ancient, Unified Mechanism for Metformin Growth Inhibition in C. elegans and Cancer
Cell ·Lianfeng Wu, Ben Zhou, Noriko Oshiro-Rapley, Man Li, João A. Paulo, Christopher M. Webster, Fan Mou, Michael C. Kacergis, Michael E. Talkowski, Christopher E. Carr, Steven P. Gygi, Bin Zheng, Alexander A. Soukas
2016172
8
Next-Generation Sequencing Strategies Enable Routine Detection of Balanced Chromosome Rearrangements for Clinical Diagnostics and Genetic Research
The American Journal of Human Genetics ·Michael E. Talkowski, Carl Ernst, Adrian Heilbut, Colby Chiang, Carrie Hanscom, Amelia M. Lindgren, Andrew Kirby, Shangtao Liu, Bhavana Muddukrishna, Toshiro K. Ohsumi, Yiping Shen, Mark L. Borowsky, Mark J. Daly, Cynthia C. Morton, James F. Gusella
2011120
9
Clinical Diagnosis by Whole-Genome Sequencing of a Prenatal Sample
New England Journal of Medicine ·Michael E. Talkowski, Zehra Ordulu, Vamsee Pillalamarri, Carol B. Benson, Ian Blumenthal, Susan A. Connolly, Carrie Hanscom, Naveed Hussain, Shahrin Pereira, Jonathan Picker, Jill A. Rosenfeld, Lisa G. Shaffer, Louise Wilkins‐Haug, James F. Gusella, Cynthia C. Morton
2012119
10
Cognitive influences in postural control of patients with unilateral vestibular loss
Gait & Posture ·Mark S. Redfern, Michael E. Talkowski, J. Richard Jennings, Joseph M. Furman
2003112
11
A network of dopaminergic gene variations implicated as risk factors for schizophrenia
Human Molecular Genetics ·Michael E. Talkowski, George Kirov, Mikhil Bamne, Lyudmila Georgieva, Gonzalo E. Torres, Hader Mansour, Kodavali V. Chowdari, Vihra Milanova, Joel Wood, Lora McClain, Konasale M. Prasad, Brian H. Shirts, Jianping Zhang, Michael O’Donovan, Michael J. Owen, Bernie Devlin, Vishwajit L. Nimgaonkar
2007105
12
Transcriptional Consequences of 16p11.2 Deletion and Duplication in Mouse Cortex and Multiplex Autism Families
The American Journal of Human Genetics ·Ian Blumenthal, Ashok Ragavendran, Serkan Erdin, Lambertus Klei, Aarathi Sugathan, Jolene R. Guide, Poornima Manavalan, Julian Q. Zhou, Vanessa C. Wheeler, Joshua Z. Levin, Carl Ernst, Kathryn Roeder, Bernie Devlin, James F. Gusella, Michael E. Talkowski
201488
13
Genetic polymorphisms of the RGS4 and dorsolateral prefrontal cortex morphometry among first episode schizophrenia patients
Molecular Psychiatry ·Konasale M. Prasad, Kodavali V. Chowdari, Vishwajit L. Nimgaonkar, Michael E. Talkowski, David A. Lewis, Matcheri S. Keshavan
200483
14
Ectopic expression of RAD52 and dn53BP1 improves homology-directed repair during CRISPR–Cas9 genome editing
Nature Biomedical Engineering ·Bruna S. Paulsen, Pankaj Kumar Mandal, Richard L. Frock, Bariş Boyraz, Rachita Yadav, Srigokul Upadhyayula, Paula Gutierrez‐Martinez, Wataru Ebina, Anders Fasth, Tomas Kirchhausen, Michael E. Talkowski, Suneet Agarwal, Frederick W. Alt, Derrick J. Rossi
201780
15
SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility
The American Journal of Human Genetics ·Samantha L.P. Schilit, Shreya Menon, Corinna Friedrich, Tammy Kammin, Ellen Wilch, Carrie Hanscom, Sizun Jiang, Sabine Kliesch, Michael E. Talkowski, Frank Tüttelmann, Amy J. MacQueen, Cynthia C. Morton
201966
16
Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR
Nature Neuroscience ·Derek J.C. Tai, Ashok Ragavendran, Poornima Manavalan, Alexei Stortchevoi, Catarina M. Seabra, Serkan Erdin, Ryan L. Collins, Ian Blumenthal, Xiaoli Chen, Yiping Shen, Mustafa Şahin, Chengsheng Zhang, Charles Lee, James F. Gusella, Michael E. Talkowski
201653
17
Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palate
Human Genetics ·Amelia M. Lindgren, Tatiana Hoyos, Michael E. Talkowski, Carrie Hanscom, Ian Blumenthal, Colby Chiang, Carl Ernst, Shahrin Pereira, Zehra Ordulu, Carol L. Clericuzio, Joanne M. Drautz, Jill A. Rosenfeld, Lisa G. Shaffer, Lea Velsher, Tania Pynn, Joris Vermeesch, David J. Harris, James F. Gusella, Eric C. Liao, Cynthia C. Morton
201351
18
Autism Spectrum Disorder Genetics
Harvard Review of Psychiatry ·Michael E. Talkowski, Eric Vallabh Minikel, James F. Gusella
201451
19
De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families
The American Journal of Human Genetics ·Jonathan R. Belyeu, Harrison Brand, Harold Wang, Xuefang Zhao, Brent S. Pedersen, Julie Feusier, Meenal Gupta, Thomas J. Nicholas, Joseph Brown, Lisa Baird, Bernie Devlin, Stephan Sanders, Lynn B. Jorde, Michael E. Talkowski, Aaron R. Quinlan
202150
20
Novel, Replicated Associations Between Dopamine D3 Receptor Gene Polymorphisms and Schizophrenia in Two Independent Samples
Biological Psychiatry ·Michael E. Talkowski, Hader Mansour, Kodavali V. Chowdari, Joel Wood, Allison Butler, Panchami G. Varma, Suman Prasad, Prachi Semwal, Triptish Bhatia, Smita N. Deshpande, Bernie Devlin, B.K. Thelma, Vishwajit L. Nimgaonkar
200649

About Michael E. Talkowski

Michael E. Talkowski is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Cognitive Neuroscience and Plant Science, having authored 100 papers that have together received 4.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (33 papers), Genomics and Rare Diseases (23 papers), Genetics and Neurodevelopmental Disorders (19 papers), CRISPR and Genetic Engineering (13 papers), Genetic Associations and Epidemiology (11 papers), Congenital heart defects research (11 papers), Autism Spectrum Disorder Research (9 papers) and Chromosomal and Genetic Variations (8 papers). The work is most often cited by research in Aging (135 citations), Genetics (1.9k citations), Business and International Management (123 citations), Molecular Biology (2.7k citations) and Biological Psychiatry (65 citations). Michael E. Talkowski has collaborated with scholars based in United States, United Kingdom and Italy. Frequent 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. Their work appears in journals such as The American Journal of Human Genetics, Schizophrenia Bulletin, European Neuropsychopharmacology, Nature Communications and Human Molecular Genetics.

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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