Steven A. McCarroll

214.4k total citations · 14 hit papers
108 papers, 23.5k citations indexed

About

Steven A. McCarroll is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Steven A. McCarroll has authored 108 papers receiving a total of 23.5k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Genetics, 52 papers in Molecular Biology and 10 papers in Plant Science. Recurrent topics in Steven A. McCarroll's work include Genomic variations and chromosomal abnormalities (40 papers), Genetic Associations and Epidemiology (31 papers) and Genomics and Rare Diseases (29 papers). Steven A. McCarroll is often cited by papers focused on Genomic variations and chromosomal abnormalities (40 papers), Genetic Associations and Epidemiology (31 papers) and Genomics and Rare Diseases (29 papers). Steven A. McCarroll collaborates with scholars based in United States, United Kingdom and Sweden. Steven A. McCarroll's co-authors include James Nemesh, Evan Z. Macosko, Melissa Goldman, Nolan Kamitaki, David Altshuler, Robert E. Handsaker, Joshua R. Sanes, Aviv Regev, Karthik Shekhar and Anindita Basu and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Steven A. McCarroll

108 papers receiving 23.2k citations

Hit Papers

5 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.

Highly Parallel Genome-wide Expression Profiling of Individual Cells Using Nanoliter Droplets

2015 4.6k citations James Nemesh, Melissa Goldman et al. profile →
Genes that act downstream of DAF-16 to influence the lifespan of Caenorhabditis elegans

2003 1.8k citations Coleen T. Murphy, Steven A. McCarroll et al. Nature profile →
Schizophrenia risk from complex variation of complement component 4

2016 1.5k citations Giulio Genovese, Robert E. Handsaker et al. Nature profile →
Genome-wide detection and characterization of positive selection in human populations

2007 1.4k citations Steven A. McCarroll et al. Nature profile →
Single-Cell RNA Sequencing of Microglia throughout the Mouse Lifespan and in the Injured Brain Reveals Complex Cell-State Changes

2018 1.4k citations Alec Wysoker, James Nemesh et al. profile →
Molecular Diversity and Specializations among the Cells of the Adult Mouse Brain

2018 943 citations Alec Wysoker, Melissa Goldman et al. profile →
Cell diversity and network dynamics in photosensitive human brain organoids

2017 870 citations Melissa Goldman, Steven A. McCarroll et al. Nature profile →
Comprehensive Classification of Retinal Bipolar Neurons by Single-Cell Transcriptomics

2016 722 citations James Nemesh, Melissa Goldman et al. profile →
Copy number variation: New insights in genome diversity

2006 592 citations Steven A. McCarroll, David Altshuler et al. profile →
A molecular census of arcuate hypothalamus and median eminence cell types

2017 560 citations Melissa Goldman, Steven A. McCarroll et al. Nature Neuroscience profile →
Common deletion polymorphisms in the human genome

2005 527 citations Steven A. McCarroll, Mark J. Daly et al. Nature Genetics profile →
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

2008 507 citations Joshua M. Korn, Steven A. McCarroll et al. Nature Genetics profile →
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

2018 293 citations Alexander Gusev, Nicholas Mancuso et al. Nature Genetics profile →
Long somatic DNA-repeat expansion drives neurodegeneration in Huntington’s disease

2025 45 citations Robert E. Handsaker, Nora Reed et al. profile →

Peers

Countries citing papers authored by Steven A. McCarroll

Since Specialization

Citations

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

Fields of papers citing papers by Steven A. McCarroll

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Steven A. McCarroll. 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 Steven A. McCarroll. The network helps show where Steven A. McCarroll may publish in the future.

Co-authorship network of co-authors of Steven A. McCarroll

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

#	Work	Indexed citations
1	Higher dopamine D1 receptor expression in prefrontal parvalbumin neurons underlies higher distractibility in marmosets versus macaques 2025 ·Communications Biology ·Mary Kate P. Joyce, (unknown), Fenna M. Krienen, Jude F. Mitchell, Shaojie Ma, Wataru Inoue, Anirvan S. Nandy, Dibyadeep Datta, Alvaro Duque, Jon I. Arellano, Rahul Gupta, Guillermo González‐Burgos, David A. Lewis, Nenad Šestan, Steven A. McCarroll, Julio Martínez-Trujillo, Seán Froudist‐Walsh, Amy F.T. Arnsten	2
2	High-dimensional phenotyping to define the genetic basis of cellular morphology 2024 ·Nature Communications ·Matthew Tegtmeyer, Jatin Arora, Samira Asgari, Beth A. Cimini, Ajay Nadig, (unknown), (unknown), Gregory P. Way, Erin Weisbart, Aparna Nathan, Tiffany Amariuta, Kevin Eggan, Marzieh Haghighi, Steven A. McCarroll, Luke J. O’Connor, Anne E. Carpenter, Shantanu Singh, Ralda Nehme, Soumya Raychaudhuri	21
3	BCFtools/liftover: an accurate and comprehensive tool to convert genetic variants across genome assemblies 2024 ·Bioinformatics ·Giulio Genovese, Nicole B. Rockweiler, Bryan R. Gorman, Tim B. Bigdeli, (unknown), Carlos N. Pato, (unknown), Steven A. McCarroll	27
4	Robust induction of functional astrocytes using NGN2 expression in human pluripotent stem cells 2023 ·iScience ·Martin H. Berryer, Matthew Tegtmeyer, Loïc Binan, Vera Valakh, (unknown), (unknown), (unknown), (unknown), Daniel Meyer, Olli Pietiläinen, Francesca Rapino, Samouil L. Farhi, Lee L. Rubin, Steven A. McCarroll, Ralda Nehme, Lindy E. Barrett	9
5	Efficient generation of lower induced motor neurons by coupling Ngn2 expression with developmental cues 2023 ·Cell Reports ·Francesco Limone, Irune Guerra San Juan, Jana M. Mitchell, (unknown), (unknown), Daniel Meyer, Sulagna Ghosh, Alexander Benavides Couto, Joseph R. Klim, Brian Joseph, (unknown), Curtis J. Mello, James Nemesh, (unknown), Matthijs Verhage, Steven A. McCarroll, Olli Pietiläinen, Ralda Nehme, Kevin Eggan	17
6	Protein-coding repeat polymorphisms strongly shape diverse human phenotypes 2021 ·Science ·Ronen E. Mukamel, Robert E. Handsaker, Maxwell A. Sherman, Alison R. Barton, Yiming Zheng, Steven A. McCarroll, Po‐Ru Loh	92
7	Early role for a Na ⁺ ,K ⁺ -ATPase ( ATP1A3 ) in brain development 2021 ·Proceedings of the National Academy of Sciences ·Richard S. Smith, Marta Florio, Shyam K. Akula, Jennifer E. Neil, Yidi Wang, Robert Hill, Melissa Goldman, Christopher D. Mullally, Nora Reed, Luis Bello‐Espinosa, Laura Flores‐Sarnat, Fabíola Paoli Monteiro, Erasmo Barbante Casella, Filippo Pinto e Vairo, Éva Morava, A. James Barkovich, Joseph Gonzalez–Heydrich, Catherine A. Brownstein, Steven A. McCarroll, Christopher A. Walsh	28
8	Insights into variation in meiosis from 31,228 human sperm genomes 2020 ·Nature ·Avery Davis Bell, Curtis J. Mello, James Nemesh, Sara A. Brumbaugh, Alec Wysoker, Steven A. McCarroll	70
9	The genomics of major psychiatric disorders in a large pedigree from Northern Sweden 2019 ·Translational Psychiatry ·Jin Szatkiewicz, James J. Crowley, Annelie Nordin Adolfsson, Karolina A. Åberg, Maaike Alaerts, Giulio Genovese, Steven A. McCarroll, Jurgen Del‐Favero, Rolf Adolfsson, Patrick F. Sullivan	11
10	Analysis scripts for: Insights about variation in meiosis from 31,228 human sperm genomes 2019 ·Figshare ·Avery Davis Bell, Curtis J. Mello, James Nemesh, Sara A. Brumbaugh, Alec Wysoker, Steven A. McCarroll	1
11	Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights breakdown → 2018 ·Nature Genetics ·Alexander Gusev, Nicholas Mancuso, Hyejung Won, Maria Kousi, Hilary K. Finucane, Yakir Reshef, Lingyun Song, Alexias Safi, Steven A. McCarroll, Benjamin M. Neale, Roel A. Ophoff, Michael O’Donovan, Gregory E. Crawford, Daniel H. Geschwind, Nicholas Katsanis, Patrick F. Sullivan, Bogdan Paşaniuc, Alkes L. Price	293
12	Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia 2017 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Ganna Leonenko, Alexander Richards, James Walters, Andrew Pocklington, Kimberly Chambert, (unknown), Sally I. Sharp, Niamh L. O’Brien, David Curtis, Nicholas Bass, Andrew McQuillin, Christina M. Hultman, Jennifer L. Moran, Steven A. McCarroll, Pamela Sklar, Benjamin M. Neale, Peter Holmans, Michael J. Owen, Patrick F. Sullivan, Michael O’Donovan	16
13	Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia 2016 ·Nature Neuroscience ·Giulio Genovese, Menachem Fromer, Eli A. Stahl, Douglas M. Ruderfer, Kimberly Chambert, Mikael Landén, Jennifer L. Moran, Shaun Purcell, Pamela Sklar, Patrick F. Sullivan, Christina M. Hultman, Steven A. McCarroll	276
14	Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia 2015 ·Neuron ·Andrew Pocklington, Elliott Rees, James Walters, Jun Han, David H. Kavanagh, Kimberly Chambert, Peter Holmans, Jennifer L. Moran, Steven A. McCarroll, George Kirov, Michael O’Donovan, Michael J. Owen	126
15	De novo CNVs in bipolar affective disorder and schizophrenia 2014 ·Human Molecular Genetics ·Lyudmila Georgieva, Elliott Rees, Jennifer L. Moran, Kimberly D. Chambert, Vihra Milanova, Nicholas Craddock, Shaun Purcell, Pamela Sklar, Steven A. McCarroll, Peter Holmans, Michael O’Donovan, Michael J. Owen, George Kirov	56
16	Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample 2013 ·Molecular Psychiatry ·Jin Szatkiewicz, Benjamin M. Neale, (unknown), Menachem Fromer, Jacqueline I. Goldstein, Jennifer L. Moran, Kimberly Chambert, (unknown), Patrik K. E. Magnusson, (unknown), Pamela Sklar, Shaun Purcell, Steven A. McCarroll, Patrick F. Sullivan	21
17	Mapping a New Spontaneous Preterm Birth Susceptibility Gene, IGF1R, Using Linkage, Haplotype Sharing, and Association Analysis 2011 ·PLoS Genetics ·Ritva Haataja, Minna K. Karjalainen, (unknown), Kari Teramo, (unknown), Marja Ojaniemi, Teppo Varilo, Bimal P. Chaudhari, Jevon Plunkett, Jeffrey C. Murray, Steven A. McCarroll, Leena Peltonen, Louis J. Muglia, Aarno Palotie, Mikko Hallman	53
18	Discovery and genotyping of genome structural polymorphism by sequencing on a population scale 2011 ·Nature Genetics ·Robert E. Handsaker, Joshua M. Korn, James Nemesh, Steven A. McCarroll	227
19	Evaluation of Common Variants in the Six Known Maturity-Onset Diabetes of the Young (MODY) Genes for Association With Type 2 Diabetes 2007 ·Diabetes ·Wendy Winckler, Michael N. Weedon, Robert Graham, Steven A. McCarroll, Shaun Purcell, Peter Almgren, (unknown), Daniel Gaudet, Kristina Bengtsson Boström, Mark Walker, G. A. Hitman, Andrew T. Hattersley, Mark I. McCarthy, Kristin Ardlie, Joel N. Hirschhorn, Mark J. Daly, Timothy M. Frayling, Leif Groop, David Altshuler	130
20	Comparing genomic expression patterns across species identifies shared transcriptional profile in aging 2004 ·Nature Genetics ·Steven A. McCarroll, Coleen T. Murphy, Sige Zou, Scott D. Pletcher, Chen-Shan Chin, Yuh Nung Jan, Cynthia Kenyon, Cornelia I. Bargmann, Hao Li	335

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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