Jennifer Miller

4.2k citations
61 papers · 2.6k indexed · 1 hit paper · h-index 23
Topics
Genetic Syndromes and Imprinting (40 papers)Genetics and Neurodevelopmental Disorders (18 papers)Epigenetics and DNA Methylation (14 papers)

In The Last Decade

Jennifer Miller

58 papers receiving 2.6k citations

Hit Papers

Prader-Willi syndrome201220262016202120122505007501000

Peers

Jennifer Miller
Comparison fields: 5 of 89
  • Genetics 1.9k
  • Molecular Biology 956
  • Pediatrics, Perinatology and Child Health 537
  • Surgery 376
  • Cognitive Neuroscience 192
Replace Sylvie Brailly‐Tabard with:
Sylvie Brailly‐Tabard France
M. Tauber France
Antonino Crinò Italy
Gwénaëlle Diene France
Vanja A. Holm United States
Sarah Voisin Australia
M. Tauber France
Ha Trang France
Garry L. Warne Australia
Nick Goeden United States
Jennifer Miller relative to Sylvie Brailly‐Tabard France Sylvie Brailly‐Tabard's profile →
Citations per field
00.5×2.7×
Sylvie Brailly‐Tabard · 1×
Citations per year

Countries citing papers authored by Jennifer Miller

Since Specialization
Citations

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

Fields of papers citing papers by Jennifer Miller

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer Miller

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

All Works

20 of 20 papers shown
#WorkIndexed citations
1 0
2 1
3 0
4 1
5 1
6 3
7 2
8 2
9 5
10 3
11 9
12 1
13
Prader-Willi syndromebreakdown →
1016
14 45
15 14
16 56
17 35
18 67
19 19
20 20

About Jennifer Miller

Jennifer Miller is a scholar working on Genetics, Endocrine and Autonomic Systems and Pediatrics, Perinatology and Child Health, having authored 61 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (40 papers), Genetics and Neurodevelopmental Disorders (18 papers) and Epigenetics and DNA Methylation (14 papers). The work is most often cited by research in Genetics (1.9k citations), Pediatrics, Perinatology and Child Health (537 citations) and Endocrine and Autonomic Systems (181 citations). Jennifer Miller has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Daniel J. Driscoll, Suzanne B. Cassidy, Stuart Schwartz, Merlin G. Butler, Jonathan J. Shuster, Virginia Kimonis, Elisabeth M. Dykens, Anthony P. Goldstone, June‐Anne Gold and Mary Wagner. Their work appears in journals such as SHILAP Revista de lepidopterología, Journal of the American College of Cardiology and The Journal of Clinical Endocrinology & Metabolism.

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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