Ryan L. Collins

28.4k citations

28 papers · 1.3k indexed · 1 hit paper · h-index 15

Impact in

Business and International Management top 2%
- Innovation and Socioeconomic Development
Aging top 5%

Papers in

Aging 1
Genetics 13
- Genomics and Rare Diseases 8
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 2

Co-authors: Michael E. Talkowski Harrison Brand Chad A. Cowan Kiran Musunuru Ashok Ragavendran Serkan Erdin Qiurong Ding Adrian Veres
Journals: Cell stem cell (3 papers)The American Journal of Human Genetics (2 papers)European Neuropsychopharmacology (2 papers)Nature Genetics (1 paper)Journal of Pharmacology and Experimental Therapeutics (1 paper)
Partner nations: United States Denmark Germany

In The Last Decade

Ryan L. Collins

27 papers receiving 1.2k citations

Hit Papers

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Efficient Ablation of Genes in Human Hematopoietic Stem and Effector Cells using CRISPR/Cas9 2014 · 379 citations

Peers

Countries citing papers authored by Ryan L. Collins

Since Specialization

Citations

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

Fields of papers citing papers by Ryan L. Collins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ryan L. Collins. 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 Ryan L. Collins. The network helps show where Ryan L. Collins may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Ryan L. Collins, 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 Ryan L. Collins Line = papers co-authored together Ryan L. Collins links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Diversity and consequences of structural variation in the human genome Nature Reviews Genetics ·Ryan L. Collins, Michael E. Talkowski	2025	6
2	Integrative Analysis of Germline Rare Variants in Clear and Non–clear Cell Renal Cell Carcinoma European Urology Open Science ·Seung Hun Han, Sabrina Y. Camp, Gao Chua, Ryan L. Collins, Jose Miguel Palacios-Jaraquemada, Jihye Park, Ziad Bakouny, Cora A. Ricker, Brendan Reardon, Nicholas Moore, Eric Kofman, Chris Labaki, David A. Braun, Toni K. Choueiri, Saud H. AlDubayan, Eliezer M. Van Allen	2024	4
3	GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data Nature Genetics ·Mehrtash Babadi, Jack Fu, Samuel K. Lee, Andrey N. Smirnov, Laura D. Gauthier, Mark Walker, David Benjamin, Xuefang Zhao, Konrad J. Karczewski, Isaac Wong, Ryan L. Collins, Alba Sanchis‐Juan, Harrison Brand, Eric Banks, Michael E. Talkowski	2023	35
4	CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants online Bioinformatics ·H.N. Flippo, Eduardo Pérez‐Palma, Tobias Brünger, Pynhunlang Kharnaior, Konrad Platzer, Mehrnaz Hosseinalifam, Ludovica Montanucci, Allan Bayat, Caroline Mwende Makau, Ryan L. Collins, Michael E. Talkowski, Daniel Blankenberg, Rikke S. Møller, Johannes R. Lemke, Michael Nothnagel, Patrick May, Dennis Lal	2023	8
5	Breast-Directed Quad Shot Radiation Therapy for Effective Breast Symptoms Palliation Without Interrupting or Delaying Systemic Cancer Therapy Schedule in Patients With Neglected Breast Cancer Advances in Radiation Oncology ·Whoon Jong Kil, Ryan L. Collins, Susan A. Branton, T.J. Wilhite, Seung Uon Shin	2023	2
6	Familial thrombocytopenia due to a complex structural variant resulting in a WAC-ANKRD26 fusion transcript The Journal of Experimental Medicine ·Lara Wahlster, Jeffrey M. Verboon, Leif S. Ludwig, L. Vettorazzi, Wendy Luo, Thomas Hörnlein, Richard A. Voit, Ryan L. Collins, Kiran Garimella, Maura Costello, Katherine R. Chao, Julia K. Goodrich, Stephanie DiTroia, Anne O’Donnell‐Luria, Michael E. Talkowski, Alan D. Michelson, Alan Cantor, Vijay G. Sankaran	2021	10
7	Mutations causing Lopes-Maciel-Rodan syndrome are huntingtin hypomorphs Human Molecular Genetics ·Xuejun Ma, Yejin Lee, Douglas Barker, Kevin Correia, Franciele de Sousa Franco, Jacob M. Loupe, Ryan L. Collins, Diane Lucente, on Jaime Cortina Watson, Tammy Gillis, Jayalakshmi Srinidhi Mysore, Lance H. Rodan, Jonathan Picker, Jong‐Min Lee, David Howland, Serageldin Attia, Seung Kwak, Marcy E. MacDonald, James F. Gusella, Ihn Sik Seong	2021	20
8	Genome sequencing identifies a homozygous inversion disrupting QDPR as a cause for dihydropteridine reductase deficiency Molecular Genetics & Genomic Medicine ·杨正清, Sander Pajusalu, Monica H. Wojcik, Julia K. Goodrich, Ryan L. Collins, Renata Alcoba, German Alexander Delgado Muñoz, Nenad Blau, Kersti Lilleväli, Katrin Õunap	2020	5
9	LIMITED CONTRIBUTION OF RARE, NONCODING VARIATION TO AUTISM SPECTRUM DISORDER FROM SEQUENCING OF 2,076 GENOMES IN QUARTET FAMILIES European Neuropsychopharmacology ·Donna M. Werling, Harrison Brand, Joon‐Yong An, Matthew R. Stone, Joseph Glessner, Lingxue Zhu, Ryan L. Collins, Mark J. Daly, Matthew W. State, Aaron R. Quinlan, Gábor Marth, Kathryn Roeder, Bernie Devlin, Stephan Sanders, Michael E. Talkowski	2019	2
10	Next Generation Sequencing of Prenatal Structural Chromosomal Rearrangements Using Large-Insert Libraries Methods in molecular biology ·Benjamin Currall, Caroline Antolik, Ryan L. Collins, Michael E. Talkowski	2018	1
11	Estrogen-related receptor gamma implicated in a phenotype including hearing loss and mild developmental delay European Journal of Human Genetics ·Samantha L.P. Schilit, Benjamin Currall, Ruen Yao, Carrie Hanscom, Ryan L. Collins, Vamsee Pillalamarri, Dong-Young Lee, Tammy Kammin, Cinthya Zepeda‐Mendoza, Tarja Mononen, Ruly Oktavia Supriyani, James F. Gusella, Michael E. Talkowski, Jun Shen, Cynthia C. Morton	2016	14
12	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	2016	53
13	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	2014	378
14	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	2014	19
15	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 →	2014	379
16	Cryptic and Complex Chromosomal Aberrations in Early-Onset Neuropsychiatric Disorders The American Journal of Human Genetics ·Harrison Brand, Vamsee Pillalamarri, Ryan L. Collins, Cristiana C. A. Rocca, Colm Ó'Dúshláine, Ellen B. Braaten, Matthew R. Stone, Kimberly Chambert, Nathan D. Doty, Carrie Hanscom, Jill A. Rosenfeld, Yury Fatyhov, David Loeffler, Ryan E. Mills, Charles Lee, James F. Gusella, Steven A. McCarroll, Jordan W. Smoller, Michael E. Talkowski, Alysa E. Doyle	2014	27
17	Multifactor dimensionality reduction reveals a three-locus epistatic interaction associated with susceptibility to pulmonary tuberculosis BioData Mining ·Ryan L. Collins, Ting Hu, Christian Wejse, Giorgio Sirugo, Scott M. Williams, Jason H. Moore	2013	31
18	An information-gain approach to detecting three-way epistatic interactions in genetic association studies Journal of the American Medical Informatics Association ·Ting Hu, Yuanzhu Chen, Jeff Kiralis, Ryan L. Collins, Christian Wejse, Giorgio Sirugo, Scott M. Williams, Jason H. Moore	2013	56
19	Independent gene duplications of the YidC/Oxa/Alb3 family enabled a specialized cotranslational function Proceedings of the National Academy of Sciences ·Soledad Funes, Adnan Hasona, Heike Bauerschmitt, V. Kubelka, Frank Kauff, Ryan L. Collins, Paula J. Crowley, Sara R. Palmer, L. Jeannine Brady, Johannes M. Herrmann	2009	64
20	PRENATAL CHLORPROMAZINE EFFECTS ON LIVER, SURVIVAL AND BEHAVIOR OF MICE OFFSPRING Journal of Pharmacology and Experimental Therapeutics ·J. M. Ordy, T. Samorajski, Ryan L. Collins, C. Rolsten	1966	49

About Ryan L. Collins

Ryan L. Collins is a scholar working on Aging, Genetics, Clinical Biochemistry, Behavioral Neuroscience and Cancer Research, having authored 28 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (8 papers), CRISPR and Genetic Engineering (5 papers), Immunodeficiency and Autoimmune Disorders (2 papers), Metabolism and Genetic Disorders (2 papers), Prenatal Screening and Diagnostics (2 papers), Genomics and Phylogenetic Studies (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Business and International Management (118 citations), Aging (68 citations), Genetics (471 citations), Molecular Biology (1.0k citations) and Virology (41 citations). Ryan L. Collins has collaborated with scholars based in United States, Denmark and Germany. Frequent co-authors include Michael E. Talkowski, Harrison Brand, Chad A. Cowan, Kiran Musunuru, Ashok Ragavendran, Serkan Erdin, Qiurong Ding, Adrian Veres, Bridget S. Gosis and Alexei Stortchevoi. Their work appears in journals such as Cell stem cell, The American Journal of Human Genetics, European Neuropsychopharmacology, Nature Genetics and Journal of Pharmacology and Experimental Therapeutics.

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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