Xander Nuttle

2.1k total citations
9 papers, 397 citations indexed

About

Xander Nuttle is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Xander Nuttle has authored 9 papers receiving a total of 397 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Plant Science. Recurrent topics in Xander Nuttle's work include Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (4 papers) and Prenatal Screening and Diagnostics (2 papers). Xander Nuttle is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (4 papers) and Prenatal Screening and Diagnostics (2 papers). Xander Nuttle collaborates with scholars based in United States, Italy and Canada. Xander Nuttle's co-authors include Evan E. Eichler, Francesca Antonacci, Megan Y. Dennis, Peter H. Sudmant, Cynthia J. Curry, Susan Shafer, Richard K. Wilson, Jill A. Rosenfeld, Pieter J. de Jong and Mikhail Nefedov and has published in prestigious journals such as Cell, Nature Methods and Nature Protocols.

In The Last Decade

Xander Nuttle

9 papers receiving 391 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Xander Nuttle United States	6	257	192	94	43	28	9	397
Tara Friedrich United States	7	362 1.4×	143 0.7×	41 0.4×	65 1.5×	37 1.3×	8	524
Belén Lorente-Galdós Spain	11	131 0.5×	140 0.7×	29 0.3×	27 0.6×	31 1.1×	12	318
Susan Shafer United States	2	183 0.7×	110 0.6×	72 0.8×	20 0.5×	25 0.9×	2	275
Jonathon Keeney United States	8	192 0.7×	145 0.8×	56 0.6×	53 1.2×	8 0.3×	12	307
Carli K. Opland United States	4	503 2.0×	285 1.5×	38 0.4×	72 1.7×	30 1.1×	5	641
Nir Oksenberg United States	9	334 1.3×	160 0.8×	40 0.4×	78 1.8×	18 0.6×	12	462
Rathi Puliyadi United Kingdom	10	292 1.1×	134 0.7×	20 0.2×	54 1.3×	41 1.5×	12	516
James H. Notwell United States	8	277 1.1×	76 0.4×	79 0.8×	31 0.7×	34 1.2×	8	372
Erin Arbuckle United States	6	209 0.8×	93 0.5×	113 1.2×	79 1.8×	41 1.5×	9	448
Poornima Manavalan United States	5	326 1.3×	261 1.4×	22 0.2×	139 3.2×	48 1.7×	5	423

Countries citing papers authored by Xander Nuttle

Since Specialization

Citations

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

Fields of papers citing papers by Xander Nuttle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Xander Nuttle. 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 Xander Nuttle. The network helps show where Xander Nuttle may publish in the future.

Co-authorship network of co-authors of Xander Nuttle

This figure shows the co-authorship network connecting the top 25 collaborators of Xander Nuttle. A scholar is included among the top collaborators of Xander Nuttle 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 Xander Nuttle. Xander Nuttle is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

Black, Joshua B., Alejandro Barrera, Susan A. Berry, et al.. (2025). Activation of the imprinted Prader-Willi syndrome locus by CRISPR-based epigenome editing. Cell Genomics. 5(2). 100770–100770. 4 indexed citations

Nuttle, Xander, Benjamin Currall, Mariana Moysés‐Oliveira, et al.. (2023). Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR libraries. Cell Reports Methods. 4(1). 100672–100672. 1 indexed citations

Liao, Calwing, Mariana Moysés‐Oliveira, Xander Nuttle, et al.. (2023). Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies. Cell Genomics. 3(4). 100277–100277. 5 indexed citations

Wallace, Arianne S., Caitlin M. Hudac, Kyle J. Steinman, et al.. (2017). Longitudinal report of child with de novo 16p11.2 triplication. Clinical Case Reports. 6(1). 147–154. 5 indexed citations

Dougherty, Max L., Xander Nuttle, Osnat Penn, et al.. (2017). The birth of a human-specific neural gene by incomplete duplication and gene fusion. Genome biology. 18(1). 49–49. 29 indexed citations

Duyzend, Michael, Xander Nuttle, Bradley P. Coe, et al.. (2015). Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV. The American Journal of Human Genetics. 98(1). 45–57. 44 indexed citations

Nuttle, Xander, Andy Itsara, Jay Shendure, & Evan E. Eichler. (2014). Resolving genomic disorder–associated breakpoints within segmental DNA duplications using massively parallel sequencing. Nature Protocols. 9(6). 1496–1513. 11 indexed citations

Nuttle, Xander, John Huddleston, Brian J. O’Roak, et al.. (2013). Rapid and accurate large-scale genotyping of duplicated genes and discovery of interlocus gene conversions. Nature Methods. 10(9). 903–909. 24 indexed citations

Dennis, Megan Y., Xander Nuttle, Peter H. Sudmant, et al.. (2012). Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication. Cell. 149(4). 912–922. 274 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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