Emma Howard

2.9k citations
32 papers · 685 · h-index 12

Impact in

    • Gastrointestinal motility and disorders
  • Hepatology top 10%
    • Hepatocellular Carcinoma Treatment and Prognosis

Papers in

    • Intestinal Malrotation and Obstruction Disorders 6
    • Pediatric Hepatobiliary Diseases and Treatments 4
    • Congenital gastrointestinal and neural anomalies 2
    • BRCA gene mutations in cancer 3
    • Genomic variations and chromosomal abnormalities 2
    • Genomics and Rare Diseases 2

Emma Howard

28 papers receiving 666 citations

Peers

Emma Howard
Comparison fields: 5 of 84
  • Gastroenterology 79
  • Hepatology 77
  • Genetics 189
  • Surgery 202
  • Pharmacy 15
Replace P Muona with:
P Muona Finland
Ichiro Abe Japan
Mitsuko R. Ito Japan
Manuel J. Amador-Patarroyo United States
Robert Sullivan United States
Dimitrios N. Papachristou United States
N Weber Australia
Keita Utsunomiya Japan
Gabriella Zara Italy
Gianfilippo Bagnato Italy
Emma Howard relative to P Muona Finland P Muona's profile →
Citations per field
00.5×6.4×
P Muona · 1×
Citations per year

Countries citing papers authored by Emma Howard

Since Specialization
Citations

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

Fields of papers citing papers by Emma Howard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 32 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2008148
2 201492
3 199986
4 199583
5 200158
6 201235
7 200728
8 198323
9 197118
10 201915
11
Surgery in children with homozygous sickle cell anaemia.
197913
12 199111
13 20158
14 19918
15 19968
16
Histochemistry in the diagnosis and investigation of congenital aganglionosis (Hirschsprung's disease).
19738
17 19917
18 19987
19 20105
20 20055

About Emma Howard

Emma Howard is a scholar working on Surgery, Genetics, Pulmonary and Respiratory Medicine, Urology and Epidemiology, having authored 32 papers that have together received 685 indexed citations. Recurring topics across this work include Intestinal Malrotation and Obstruction Disorders (6 papers), Pediatric Hepatobiliary Diseases and Treatments (4 papers), BRCA gene mutations in cancer (3 papers), Urological Disorders and Treatments (2 papers), Congenital gastrointestinal and neural anomalies (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Hepatocellular Carcinoma Treatment and Prognosis (2 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Gastroenterology (79 citations), Hepatology (77 citations), Genetics (189 citations), Surgery (202 citations) and Pharmacy (15 citations). Emma Howard has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Dian Donnai, Nigel Heaton, Zhongming Zhao, M. Buxton‐Thomas, Julie McGaughran, Raymond A. Clarke, Michael Edmonds, J. L. Bradley, TS Purewal and Peter Watkins. Their work appears in journals such as Gut, British journal of surgery, Journal of the Royal Society of Medicine, Clinical Genetics and Journal of Medical Genetics.

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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