Hope Northrup

18.9k citations
156 papers · 6.1k indexed · 1 hit paper · h-index 38

Impact in

  • Physiology top 0.5%
    • Tuberous Sclerosis Complex Research
    • Histiocytic Disorders and Treatments
  • Genetics top 1%
    • Genetic and Kidney Cyst Diseases

Papers in

    • Tuberous Sclerosis Complex Research 57
    • Histiocytic Disorders and Treatments 14
    • Folate and B Vitamins Research 24

Hope Northrup

152 papers receiving 5.9k citations

Hit Papers

Tuberous Sclerosis Complex Consensus Conference: Revised Clinical Diagnostic Criteria 1998 · 732 citations
7321998202620072016200400600

Peers

Hope Northrup
Comparison fields: 5 of 134
  • Physiology 2.6k
  • Genetics 1.5k
  • Clinical Biochemistry 327
  • Pediatrics, Perinatology and Child Health 875
  • Rheumatology 648
Replace Manuel R. Gómez with:
Manuel R. Gómez United States
Didier Lacombe France
David Neal Franz United States
Alan Fryer United Kingdom
Christine M. Eng United States
Egbert Bakker Netherlands
Hans Scheffer Netherlands
Dicky Halley Netherlands
Sergiusz Jóźwiak Poland
Hirotomo Saitsu Japan
Hope Northrup relative to Manuel R. Gómez United States Manuel R. Gómez's profile →
Citations per field
00.5×3.7×
Manuel R. Gómez · 1×
Citations per year

Countries citing papers authored by Hope Northrup

Since Specialization
Citations

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

Fields of papers citing papers by Hope Northrup

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

20 of 20 papers shown
#Work
1 20250
2 20244
3 20247
4 20231
5 202341
6 20231
7 20223
8 20224
9 202117
10 202113
11 20204
12 202023
13 201910
14 20195
15 20184
16 20187
17 20186
18 201726
19 201518
20 201222

About Hope Northrup

Hope Northrup is a scholar working on Physiology, Rheumatology, Clinical Biochemistry, Pediatrics, Perinatology and Child Health and Genetics, having authored 156 papers that have together received 6.1k indexed citations. Recurring topics across this work include Tuberous Sclerosis Complex Research (57 papers), Folate and B Vitamins Research (24 papers), Congenital Anomalies and Fetal Surgery (22 papers), Prenatal Screening and Diagnostics (20 papers), Polyomavirus and related diseases (17 papers), Tumors and Oncological Cases (16 papers), Histiocytic Disorders and Treatments (14 papers) and Fetal and Pediatric Neurological Disorders (14 papers). The work is most often cited by research in Physiology (2.6k citations), Genetics (1.5k citations), Clinical Biochemistry (327 citations), Pediatrics, Perinatology and Child Health (875 citations) and Rheumatology (648 citations). Hope Northrup has collaborated with scholars based in United States, Germany and Canada. Frequent co-authors include E. Steve Roach, Kit Sing Au, Manuel R. Gómez, Kelly A. Volcik, Allison E. Ashley‐Koch, Susan H. Blanton, F.F.B. Elder, Darcy A. Krueger, Mary Kay Koenig and Frank Greenberg. Their work appears in journals such as Birth Defects Research Part A Clinical and Molecular Teratology, Pediatric Neurology, Journal of Child Neurology, Genetics in Medicine and Human Mutation.

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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