Xander Nuttle

2.2k citations
17 papers · 1.3k · 2 hit papers · h-index 11

Impact in

    • Neurogenesis and neuroplasticity mechanisms
  • Genetics top 5%
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases

Papers in

    • Genomic variations and chromosomal abnormalities 13
    • Genomics and Rare Diseases 5
    • Genetics and Neurodevelopmental Disorders 3
    • Congenital heart defects research 5
    • CRISPR and Genetic Engineering 2

Xander Nuttle

17 papers receiving 1.3k citations

Xander Nuttle's Hit Papers

A cross-disorder dosage sensitivity map of the human genome 2022 · 197 citations
1970+2+5Years since publication100200300

Peers

Xander Nuttle
Comparison fields: 5 of 87
  • Developmental Neuroscience 148
  • Genetics 520
  • Molecular Biology 798
  • Aging 20
  • Developmental Biology 13
Replace Edmund J. Koundakjian with:
Edmund J. Koundakjian United States
Jill A. Rosenfeld United States
Noriyuki Kishi Japan
Martin W. Breuss United States
Anne Seawright United Kingdom
Simon Zwolinski United Kingdom
Leonardo L Beccari Spain
Max L. Dougherty United States
Kay E. Davies United Kingdom
Nelle Lambert Belgium
Xander Nuttle relative to Edmund J. Koundakjian United States Edmund J. Koundakjian's profile →
Citations per field
00.5×2×4×6×8.9×
Edmund J. Koundakjian · 1×
Citations per year

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-authors

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

All Works

17 of 17 papers shown
#Work
1
Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis
Hit paper breakdown →
2018397
2 2012299
3
A cross-disorder dosage sensitivity map of the human genome
Hit paper breakdown →
2022197
4 2017104
5 201696
6 201549
7 201934
8 201732
9 201329
10 202225
11 201415
12 20239
13 20259
14 20176
15 20224
16 20231
17 20241

About Xander Nuttle

Xander Nuttle is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Cognitive Neuroscience, having authored 17 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Chromosomal and Genetic Variations (5 papers), Congenital heart defects research (5 papers), Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (3 papers), CRISPR and Genetic Engineering (2 papers), Prenatal Screening and Diagnostics (2 papers) and Autism Spectrum Disorder Research (2 papers). The work is most often cited by research in Developmental Neuroscience (148 citations), Genetics (520 citations), Molecular Biology (798 citations), Aging (20 citations) and Developmental Biology (13 citations). Xander Nuttle has collaborated with scholars based in United States, Italy and Switzerland. Frequent co-authors include Evan E. Eichler, Francesca Antonacci, Megan Y. Dennis, Cynthia J. Curry, Susan Shafer, Mikhail D. Nefedov, Saba Sajjadian, Maika Malig, Richard K. Wilson and Peter H. Sudmant. Their work appears in journals such as The American Journal of Human Genetics, Cell, Cell Genomics, Nature Ecology & Evolution and Cell Reports Methods.

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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