John B. Moeschler

6.7k citations
62 papers · 2.6k indexed · h-index 25
Topics
Genomic variations and chromosomal abnormalities (21 papers)Genetics and Neurodevelopmental Disorders (17 papers)Prenatal Screening and Diagnostics (15 papers)

In The Last Decade

John B. Moeschler

61 papers receiving 2.4k citations

Peers

John B. Moeschler
Comparison fields: 5 of 123
  • Genetics 1.7k
  • Molecular Biology 995
  • Pediatrics, Perinatology and Child Health 558
  • Cognitive Neuroscience 399
  • Clinical Psychology 216
Replace Petter Strømme with:
Petter Strømme Norway
Vandana Shashi United States
Allyn McConkie‐Rosell United States
Arthur S. Aylsworth United States
Brian Hon‐Yin Chung Hong Kong
Michael M. Kaback United States
Albert E. Chudley Canada
John Dean United Kingdom
Cynthia M. Powell United States
Howard M. Saal United States
John B. Moeschler relative to Petter Strømme Norway Petter Strømme's profile →
Citations per field
00.5×1.5×1.9×
Petter Strømme · 1×
Citations per year

Countries citing papers authored by John B. Moeschler

Since Specialization
Citations

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

Fields of papers citing papers by John B. Moeschler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John B. Moeschler. 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 John B. Moeschler. The network helps show where John B. Moeschler may publish in the future.

Co-authorship network of co-authors of John B. Moeschler

This figure shows the co-authorship network connecting the top 25 collaborators of John B. Moeschler. A scholar is included among the top collaborators of John B. Moeschler 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 John B. Moeschler. John B. Moeschler 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 93
2 352
3 168
4 4
5 27
6 13
7 57
8 37
9 152
10 78
11 166
12 266
13 24
14 16
15 11
16 7
17 18
18 11
19
Further delineation of the 10p deletion syndrome.
13
20 24

About John B. Moeschler

John B. Moeschler is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Genetics, having authored 62 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (21 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Prenatal Screening and Diagnostics (15 papers). The work is most often cited by research in Genetics (1.7k citations), Pediatrics, Perinatology and Child Health (558 citations) and Cognitive Neuroscience (399 citations). John B. Moeschler has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Michael Shevell, John M. Graham, Marilyn C. Jones, John M. Opitz, Joan M. Stoler, Rizwan Hamid, Beth A. Tarini, Emily Chen, Robert A. Saul and Debra Freedenberg. Their work appears in journals such as Nature Genetics, Neurology and PEDIATRICS.

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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026