Nicholas Lench

9.9k citations
107 papers · 5.5k · 2 hit papers · h-index 36

Impact in

Papers in

    • RNA regulation and disease 8
    • Connexins and lens biology 6
    • Inflammatory Bowel Disease 9
    • Genomic variations and chromosomal abnormalities 8
    • Genomics and Rare Diseases 7

Nicholas Lench

105 papers receiving 5.3k citations

Nicholas Lench's Hit Papers

Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study 2013 · 415 citations
4150+9+19Years since publication2505007501000

Peers

Nicholas Lench
Comparison fields: 5 of 127
  • Sensory Systems 1.2k
  • Endocrine and Autonomic Systems 270
  • Genetics 1.2k
  • Neurology 320
  • Molecular Biology 2.4k
Replace Leopoldo Zelante with:
Leopoldo Zelante Italy
David P. Kelsell United Kingdom
Mustafa Tekin United States
Susan H. Blanton United States
Moshe Frydman Israel
Patrick J. Willems Belgium
Sandrine Marlin France
William Reardon United Kingdom
Maria Bitner‐Glindzicz United Kingdom
Niklas Dahl Sweden
Nicholas Lench relative to Leopoldo Zelante Italy Leopoldo Zelante's profile →
Citations per field
00.5×1.5×
Leopoldo Zelante · 1×
Citations per year

Countries citing papers authored by Nicholas Lench

Since Specialization
Citations

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

Fields of papers citing papers by Nicholas Lench

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 107 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
Hit paper breakdown →
19971144
2
Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study
Hit paper breakdown →
2013415
3 1987278
4 1988262
5 2001258
6 1998196
7 2012153
8 2015131
9 1998119
10 2015112
11 1995110
12 2013101
13 201491
14 199184
15 200081
16 199980
17 199774
18 199572
19 199468
20 201467

About Nicholas Lench

Nicholas Lench is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Surgery and Rheumatology, having authored 107 papers that have together received 5.5k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (10 papers), Hearing, Cochlea, Tinnitus, Genetics (9 papers), Inflammatory Bowel Disease (9 papers), RNA regulation and disease (8 papers), Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (7 papers), Bone and Dental Protein Studies (6 papers) and Connexins and lens biology (6 papers). The work is most often cited by research in Sensory Systems (1.2k citations), Endocrine and Autonomic Systems (270 citations), Genetics (1.2k citations), Neurology (320 citations) and Molecular Biology (2.4k citations). Nicholas Lench has collaborated with scholars based in United Kingdom, United States and Belgium. Frequent co-authors include R Mueller, David P. Kelsell, G. Parry, Howard P. Stevens, I.M. Leigh, J Liang, John Dunlop, G B Winter, Lyn S. Chitty and Brandon J. Wainwright. Their work appears in journals such as Nucleic Acids Research, European Journal of Human Genetics, The American Journal of Human Genetics, Journal of Medical Genetics and Gastroenterology.

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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