Catherine Boucher

1.0k citations
15 papers · 681 indexed · h-index 12

Impact in

Papers in

    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
    • Genetic Syndromes and Imprinting 4
    • Genetic and Kidney Cyst Diseases 4

Catherine Boucher

15 papers receiving 668 citations

Peers

Catherine Boucher
Comparison fields: 5 of 74
  • Genetics 336
  • Cellular and Molecular Neuroscience 191
  • Molecular Biology 530
  • Reproductive Medicine 58
  • Neurology 45
Replace M. Geppert with:
M. Geppert Germany
Yunmin Li United States
Prachee Avasthi United States
Reenal Pattni United States
Bryan P. Haines Australia
Christian W. Ehrenfels United States
Song‐Ro Yoon United States
Esther P. Leeflang United States
Alex Magee United Kingdom
C E de Die-Smulders Netherlands
Catherine Boucher relative to M. Geppert Germany M. Geppert's profile →
Citations per field
00.5×1.5×2.2×
M. Geppert · 1×
Citations per year

Countries citing papers authored by Catherine Boucher

Since Specialization
Citations

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

Fields of papers citing papers by Catherine Boucher

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

15 of 15 papers shown
#Work
1 20239
2 201018
3 200634
4 200613
5 200450
6 200133
7 200111
8 200140
9 200031
10 2000103
11
The critical region of overlap defining the AZFa male infertility interval of proximal Yq contains three transcribed sequences.
199987
12 199754
13 199645
14 19966
15 1995147

About Catherine Boucher

Catherine Boucher is a scholar working on Developmental Biology, Genetics, Reproductive Medicine, Cellular and Molecular Neuroscience and Molecular Biology, having authored 15 papers that have together received 681 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Genetic Syndromes and Imprinting (4 papers), Genetic and Kidney Cyst Diseases (4 papers), Genetic Neurodegenerative Diseases (3 papers), Mitochondrial Function and Pathology (2 papers), Chromosomal and Genetic Variations (2 papers), Renal and related cancers (2 papers) and Sexual Differentiation and Disorders (2 papers). The work is most often cited by research in Genetics (336 citations), Cellular and Molecular Neuroscience (191 citations), Molecular Biology (530 citations), Reproductive Medicine (58 citations) and Neurology (45 citations). Catherine Boucher has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Keith Johnson, Carole A. Sargent, Richard Sandford, Patricia Blanco, Nabeel A. Affara, Michael Mitchell, Nessa Carey, Michael J. Siciliano, Catherine Winchester and Mark E.S. Bailey. Their work appears in journals such as Genomics, Human Molecular Genetics, Gene, Cells and Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.

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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