Nicholas Lench

9.9k citations
110 papers · 5.7k · 2 hit papers · h-index 37

Impact in

Papers in

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

Nicholas Lench

106 papers receiving 5.5k 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 · 428 citations
4280+9+19Years since publication2505007501000

Peers

Nicholas Lench
Comparison fields: 5 of 127
  • Sensory Systems 1.3k
  • Endocrine and Autonomic Systems 285
  • Genetics 1.2k
  • Neurology 338
  • Otorhinolaryngology 145
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
Helmut Fuchs Germany
Maria Bitner‐Glindzicz United Kingdom
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 110 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 →
19971192
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 →
2013428
3 1987291
4 1988266
5 2001263
6 1998202
7 2012160
8 2015140
9 1998124
10 2015119
11 1995113
12 2013109
13 201493
14 199184
15 200083
16 199982
17 199777
18 199577
19 201469
20 199469

About Nicholas Lench

Nicholas Lench is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Surgery and Sensory Systems, having authored 110 papers that have together received 5.7k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (11 papers), Hearing, Cochlea, Tinnitus, Genetics (10 papers), Inflammatory Bowel Disease (9 papers), Genomic variations and chromosomal abnormalities (9 papers), RNA regulation and disease (8 papers), Genomics and Rare Diseases (8 papers), Connexins and lens biology (7 papers) and Bone and Dental Protein Studies (6 papers). The work is most often cited by research in Sensory Systems (1.3k citations), Endocrine and Autonomic Systems (285 citations), Genetics (1.2k citations), Neurology (338 citations) and Otorhinolaryngology (145 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, John Dunlop, J Liang, G B Winter, Lyn S. Chitty and Brandon J. Wainwright. Their work appears in journals such as European Journal of Human Genetics, Nucleic Acids Research, 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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