Ashley D. Sanders

6.6k citations

22 papers · 724 indexed · h-index 15

Co-authors: Peter M. Lansdorp Ester Falconer Mark Hills David Porubský Victor Guryev Jan O. Korbel Diana C.J. Spierings Tobias Marschall
Topics: Genomic variations and chromosomal abnormalities (10 papers)Chromosomal and Genetic Variations (8 papers)Cancer Genomics and Diagnostics (8 papers)
Cited by: Genetics Molecular Biology Cancer Research
Journals: Nature Communications Nature Genetics Blood
Partner nations: Germany United States Canada

In The Last Decade

Ashley D. Sanders

22 papers receiving 722 citations

Peers

Countries citing papers authored by Ashley D. Sanders

Since Specialization

Citations

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

Fields of papers citing papers by Ashley D. Sanders

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ashley D. Sanders. 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 Ashley D. Sanders. The network helps show where Ashley D. Sanders may publish in the future.

Co-authorship network of co-authors of Ashley D. Sanders

This figure shows the co-authorship network connecting the top 25 collaborators of Ashley D. Sanders. A scholar is included among the top collaborators of Ashley D. Sanders 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 Ashley D. Sanders. Ashley D. Sanders 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	Cell-type-specific consequences of mosaic structural variants in hematopoietic stem and progenitor cells 2024 ·Nature Genetics ·(unknown),Hyobin Jeong,(unknown),Nuo Xu,(unknown),Benjamin Raeder,Patrick Hasenfeld,Catherine Brasseur,Tobias Rausch,Eva Benito,Johann-Christoph Jann,Daniel Nowak,(unknown),Markus Hoenicka,Andreas Liebold,Anthony D. Ho,Shimin Shuai,Hartmut Geiger,Ashley D. Sanders,Jan O. Korbel	8
2	Gaps and complex structurally variant loci in phased genome assemblies 2023 ·Genome Research ·David Porubský,Mitchell R. Vollger,William T. Harvey,Allison N. Rozanski,Peter Ebert,Glenn Hickey,Patrick Hasenfeld,Ashley D. Sanders,Catherine Brasseur,Jan O. Korbel,Benedict Paten,Tobias Marschall,Evan E. Eichler	23
3	Family income is not significantly associated with T1w/T2w ratio in the Human Connectome Project in Development 2023 ·Imaging Neuroscience ·David G. Weissman,Graham L. Baum,Ashley D. Sanders,Maya L. Rosen,Deanna M. Barch,Katie A. McLaughlin,Leah H. Somerville	2
4	Inversion polymorphism in a complete human genome assembly 2023 ·Genome biology ·David Porubský,William T. Harvey,Allison N. Rozanski,Jana Ebler,Wolfram Höps,Hufsah Ashraf,Patrick Hasenfeld,Benedict Paten,Ashley D. Sanders,Tobias Marschall,Jan O. Korbel,Evan E. Eichler	15
5	Store‐operated calcium entry controls innate and adaptive immune cell function in inflammatory bowel disease 2022 ·EMBO Molecular Medicine ·Marilena Letizia,Yin‐Hu Wang,Ulrike Kaufmann,(unknown),(unknown),(unknown),(unknown),(unknown),Chotima Böttcher,Stephan Schlickeiser,(unknown),Megumi Yamashita,Kenneth A. Stauderman,Katherine Sun,Désirée Kunkel,Murali Prakriya,(unknown),Ashley D. Sanders,Britta Siegmund,Stefan Feske,Carl Weidinger	34
6	A high-resolution map of small-scale inversions in the gibbon genome 2022 ·Genome Research ·Ludovica Mercuri,(unknown),Alberto L’Abbate,Pietro D’Addabbo,Francesco Montinaro,Claudia Rita Catacchio,Patrick Hasenfeld,Mario Ventura,Jan O. Korbel,Ashley D. Sanders,Flavia Angela Maria Maggiolini,Francesca Antonacci	5
7	ASHLEYS: automated quality control for single-cell Strand-seq data 2021 ·Bioinformatics ·C. Gros,Ashley D. Sanders,Jan O. Korbel,Tobias Marschall,Peter Ebert	6
8	Construction of Whole Genomes from Scaffolds Using Single Cell Strand-Seq Data 2021 ·International Journal of Molecular Sciences ·Mark Hills,Ester Falconer,Kieran O’Neill,Ashley D. Sanders,Kerstin Howe,Victor Guryev,Peter M. Lansdorp	8
9	Single-cell strand sequencing of a macaque genome reveals multiple nested inversions and breakpoint reuse during primate evolution 2020 ·Genome Research ·Flavia Angela Maria Maggiolini,Ashley D. Sanders,Colin J. Shew,Arvis Sulovari,Yafei Mao,Marta Puig,Claudia Rita Catacchio,(unknown),(unknown),Ludovica Mercuri,(unknown),David Porubský,Mario Cáceres,Evan E. Eichler,Mario Ventura,Megan Y. Dennis,Jan O. Korbel,Francesca Antonacci	11
10	Recurrent inversion toggling and great ape genome evolution 2020 ·Nature Genetics ·David Porubský,Ashley D. Sanders,Wolfram Höps,PingHsun Hsieh,Arvis Sulovari,Ruiyang Li,Ludovica Mercuri,Melanie Sorensen,Shwetha C. Murali,David Gordon,Stuart Cantsilieris,Alex A. Pollen,Mario Ventura,Francesca Antonacci,Tobias Marschall,Jan O. Korbel,Evan E. Eichler	37
11	Improved assembly and variant detection of a haploid human genome using single‐molecule, high‐fidelity long reads 2019 ·Annals of Human Genetics ·Mitchell R. Vollger,Glennis A. Logsdon,Peter A. Audano,Arvis Sulovari,David Porubský,Paul Peluso,Aaron M. Wenger,Gregory T. Concepcion,Zev Kronenberg,Katherine M. Munson,Carl Baker,Ashley D. Sanders,Diana C.J. Spierings,Peter M. Lansdorp,Urvashi Surti,Michael W. Hunkapiller,Evan E. Eichler	81
12	VISOR: a versatile haplotype-aware structural variant simulator for short- and long-read sequencing 2019 ·Bioinformatics ·Davide Bolognini,Ashley D. Sanders,Jan O. Korbel,Alberto Magi,Vladimı́r Beneš,Tobias Rausch	28
13	Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus 2019 ·PLoS Genetics ·Flavia Angela Maria Maggiolini,Stuart Cantsilieris,Pietro D’Addabbo,(unknown),Bradley P. Coe,Beth L. Dumont,Ashley D. Sanders,Andy Wing Chun Pang,Mitchell R. Vollger,Orazio Palumbo,Pietro Palumbo,Maria Accadia,Massimo Carella,Evan E. Eichler,Francesca Antonacci	16
14	Strand-seq enables reliable separation of long reads by chromosome via expectation maximization 2018 ·Bioinformatics ·Maryam Ghareghani,David Porubský,Ashley D. Sanders,Sascha Meiers,Evan E. Eichler,Jan O. Korbel,Tobias Marschall	10
15	Single-cell template strand sequencing by Strand-seq enables the characterization of individual homologs 2017 ·Nature Protocols ·Ashley D. Sanders,Ester Falconer,Mark Hills,Diana C.J. Spierings,Peter M. Lansdorp	65
16	Dense and accurate whole-chromosome haplotyping of individual genomes 2017 ·Nature Communications ·David Porubský,Shilpa Garg,Ashley D. Sanders,Jan O. Korbel,Victor Guryev,Peter M. Lansdorp,Tobias Marschall	55
17	Characterizing polymorphic inversions in human genomes by single-cell sequencing 2016 ·Genome Research ·Ashley D. Sanders,Mark Hills,David Porubský,Victor Guryev,Ester Falconer,Peter M. Lansdorp	43
18	Direct chromosome-length haplotyping by single-cell sequencing 2016 ·Genome Research ·David Porubský,Ashley D. Sanders,Niek van Wietmarschen,Ester Falconer,Mark Hills,Diana C.J. Spierings,Marianna R. Bevova,Victor Guryev,Peter M. Lansdorp	34
19	DNA template strand sequencing of single-cells maps genomic rearrangements at high resolution 2012 ·Nature Methods ·Ester Falconer,Mark Hills,Ulrike Naumann,Steven S.S. Poon,Elizabeth A. Chavez,Ashley D. Sanders,Yongjun Zhao,Martin Hirst,Peter M. Lansdorp	113
20	Adult Spinal Cord Radial Glia Display a Unique Progenitor Phenotype 2011 ·PLoS ONE ·Audrey Petit,Ashley D. Sanders,Timothy E. Kennedy,Wolfram Tetzlaff,Katie Glattfelder,Rachel Dalley,Ralph B. Puchalski,Allan R. Jones,A. Jane Roskams	36

About Ashley D. Sanders

Ashley D. Sanders is a scholar working on Cancer Research, Genetics and Molecular Biology, having authored 22 papers that have together received 724 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (8 papers) and Cancer Genomics and Diagnostics (8 papers). The work is most often cited by research in Genetics (283 citations), Molecular Biology (573 citations) and Cancer Research (119 citations). Ashley D. Sanders has collaborated with scholars based in Germany, United States and Canada. Frequent co-authors include Peter M. Lansdorp, Ester Falconer, Mark Hills, David Porubský, Victor Guryev, Jan O. Korbel, Diana C.J. Spierings, Tobias Marschall, Ulrike Naumann and Evan E. Eichler. Their work appears in journals such as Nature Communications, Nature Genetics and Blood.

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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