Heather Etchevers

6.6k citations
58 papers · 3.3k · 3 hit papers · h-index 26

Impact in

Papers in

    • Congenital heart defects research 14
    • Developmental Biology and Gene Regulation 12
    • Hedgehog Signaling Pathway Studies 8
    • Ocular Disorders and Treatments 7
    • Craniofacial Disorders and Treatments 6

Heather Etchevers

58 papers receiving 3.3k citations

Hit Papers

Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations 2009 · 294 citations
2940+8+16Years since publication200400600

Peers

Heather Etchevers
Comparison fields: 5 of 114
  • Endocrine and Autonomic Systems 463
  • Developmental Neuroscience 169
  • Genetics 812
  • Molecular Biology 1.8k
  • Genetics 214
Replace Tania Attié‐Bitach with:
Tania Attié‐Bitach France
Anna B. Auerbach United States
Montserrat Milà Spain
Leopoldo Zelante Italy
Juan Pedro Martı́nez-Barberá United Kingdom
Jeh-Ping Liu United States
Tayfun Özçelık Türkiye
Hideki Enomoto Japan
Richard J. Sinke Netherlands
Patrick Edery France
Heather Etchevers relative to Tania Attié‐Bitach France Tania Attié‐Bitach's profile →
Citations per field
00.5×1.5×
Tania Attié‐Bitach · 1×
Citations per year

Countries citing papers authored by Heather Etchevers

Since Specialization
Citations

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

Fields of papers citing papers by Heather Etchevers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 58 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome
Hit paper breakdown →
2003619
2
The cephalic neural crest provides pericytes and smooth muscle cells to all blood vessels of the face and forebrain
Hit paper breakdown →
2001508
3
Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations
Hit paper breakdown →
2009294
4 2005277
5 2007162
6 2005151
7 2007148
8 199990
9 200979
10 200873
11 201972
12 200770
13 201843
14 201140
15 201636
16 201136
17 201235
18 199935
19 200834
20 200934

About Heather Etchevers

Heather Etchevers is a scholar working on Molecular Biology, Genetics, Surgery, Oncology and Genetics, having authored 58 papers that have together received 3.3k indexed citations. Recurring topics across this work include Congenital heart defects research (14 papers), Developmental Biology and Gene Regulation (12 papers), Hedgehog Signaling Pathway Studies (8 papers), Ocular Disorders and Treatments (7 papers), Cutaneous Melanoma Detection and Management (6 papers), Craniofacial Disorders and Treatments (6 papers), melanin and skin pigmentation (4 papers) and Neuroblastoma Research and Treatments (4 papers). The work is most often cited by research in Endocrine and Autonomic Systems (463 citations), Developmental Neuroscience (169 citations), Genetics (812 citations), Molecular Biology (1.8k citations) and Genetics (214 citations). Heather Etchevers has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Nicole M. Le Douarin, G Couly, Christine Vincent, Michel Vekemans, Stanislas Lyonnet, Tania Attié‐Bitach, Arnold Münnich, Jeanne Amiel, Marcy C. Speer and Loïc de Pontual. Their work appears in journals such as Development, Pigment Cell & Melanoma Research, Human Molecular Genetics, The American Journal of Human Genetics and Investigative Ophthalmology & Visual Science.

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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