Wayne Lam

2.2k total citations
22 papers, 715 citations indexed

About

Wayne Lam is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Wayne Lam has authored 22 papers receiving a total of 715 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 13 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Wayne Lam's work include Prenatal Screening and Diagnostics (6 papers), Epigenetics and DNA Methylation (5 papers) and Genetic Syndromes and Imprinting (4 papers). Wayne Lam is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Epigenetics and DNA Methylation (5 papers) and Genetic Syndromes and Imprinting (4 papers). Wayne Lam collaborates with scholars based in United Kingdom, United States and Australia. Wayne Lam's co-authors include Johanna A. Joyce, Paul N. Schofield, Wolf Reik, Izuho Hatada, Eamonn R. Maher, Dian Donnai, Tsunehiro Mukai, Trevor Cole, Sachiko Oh‐ishi and E.R. Maher and has published in prestigious journals such as Diabetes, The Journal of Urology and Cell Death and Differentiation.

In The Last Decade

Wayne Lam

21 papers receiving 705 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Wayne Lam United Kingdom 11 466 352 157 143 89 22 715
Rita Genesio Italy 19 496 1.1× 463 1.3× 92 0.6× 204 1.4× 52 0.6× 52 998
Rodger Palmer United Kingdom 13 397 0.9× 494 1.4× 76 0.5× 79 0.6× 69 0.8× 20 915
Lakshmi Mehta United States 16 403 0.9× 348 1.0× 96 0.6× 86 0.6× 57 0.6× 46 754
Ercan Mıhçı Türkiye 13 383 0.8× 264 0.8× 122 0.8× 92 0.6× 52 0.6× 65 759
Soo‐Mi Park United Kingdom 15 464 1.0× 258 0.7× 74 0.5× 46 0.3× 43 0.5× 39 794
Marie-Laure Kottler France 15 456 1.0× 406 1.2× 86 0.5× 56 0.4× 42 0.5× 23 981
Rosemarie Smith United States 11 409 0.9× 336 1.0× 151 1.0× 63 0.4× 17 0.2× 21 744
Meena Balasubramanian United Kingdom 18 310 0.7× 555 1.6× 79 0.5× 72 0.5× 63 0.7× 74 802
Boris Keren France 21 649 1.4× 515 1.5× 44 0.3× 154 1.1× 65 0.7× 70 1.1k
Gülen Eda Ütine Türkiye 14 367 0.8× 373 1.1× 66 0.4× 77 0.5× 54 0.6× 114 715

Countries citing papers authored by Wayne Lam

Since Specialization
Citations

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

Fields of papers citing papers by Wayne Lam

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wayne Lam

This figure shows the co-authorship network connecting the top 25 collaborators of Wayne Lam. A scholar is included among the top collaborators of Wayne Lam based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Wayne Lam. Wayne Lam is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Hald, Jannie Dahl, Catriona Keerie, Christopher J. Weir, et al.. (2023). Protocol of a randomised trial of teriparatide followed by zoledronic acid to reduce fracture risk in adults with osteogenesis imperfecta. BMJ Open. 13(11). e078164–e078164. 6 indexed citations
2.
Khan, Tahir Naeem, Goutham Atla, David Parry, et al.. (2023). Regulatory de novo mutations underlying intellectual disability. Life Science Alliance. 6(5). e202201843–e202201843. 3 indexed citations
3.
Lam, Wayne, Nora Shannon, Karen Knapp, et al.. (2020). Pathogenic variants causing ABL1 malformation syndrome cluster in a myristoyl-binding pocket and increase tyrosine kinase activity. European Journal of Human Genetics. 29(4). 593–603. 10 indexed citations
4.
5.
Balasubramanian, Meena, Josh Willoughby, Andrew E. Fry, et al.. (2017). Delineating the phenotypic spectrum of Bainbridge-Ropers syndrome: 12 new patients with de novo, heterozygous, loss-of-function mutations in ASXL3 and review of published literature. Journal of Medical Genetics. 54(8). 537–543. 44 indexed citations
6.
Menzies, Fiona M., Moisés Garcı́a-Arencibia, Sara Imarisio, et al.. (2014). Calpain inhibition mediates autophagy-dependent protection against polyglutamine toxicity. Cell Death and Differentiation. 22(3). 433–444. 88 indexed citations
7.
Lascaratos, Gerassimos, et al.. (2011). Adams-Oliver syndrome associated with bilateral anterior polar cataracts and optic disk drusen. Journal of American Association for Pediatric Ophthalmology and Strabismus. 15(3). 299–301. 5 indexed citations
8.
Bakrania, Preeti, Sı̇bel Aylı̇n Uğur İşerı̇, Alexander W. Wyatt, et al.. (2010). Sonic hedgehog mutations are an uncommon cause of developmental eye anomalies. American Journal of Medical Genetics Part A. 152A(5). 1310–1313. 21 indexed citations
9.
Snape, Katie, Deborah Ruddy, Martin Zenker, et al.. (2009). The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defects. American Journal of Medical Genetics Part A. 149A(8). 1860–1881. 70 indexed citations
10.
Douglas, Andrew G. L. & Wayne Lam. (2009). Extending the phenotypic spectrum of CHARGE syndrome: a case with preaxial polydactyly. Clinical Dysmorphology. 19(1). 33–34. 4 indexed citations
11.
Holloway, Susan, Birgitta Bernhard, Harry Campbell, Roseanne Cetnarskyj, & Wayne Lam. (2008). Inequality of use of Cancer Genetics Services by members of breast, ovarian and colorectal cancer families in South East Scotland. Familial Cancer. 7(3). 259–264. 8 indexed citations
12.
Holloway, Susan, Birgitta Bernhard, Harry Campbell, & Wayne Lam. (2008). Uptake of testing for BRCA1/2 mutations in South East Scotland. European Journal of Human Genetics. 16(8). 906–912. 16 indexed citations
13.
Suri, Mohnish, P. Kelehan, S. Vadeyar, et al.. (2007). WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations. American Journal of Medical Genetics Part A. 143A(19). 2312–2320. 50 indexed citations
14.
Evans, Phillip, Yasuyuki Suzuki, Michael Begg, & Wayne Lam. (2007). Can medical students from two cultures learn effectively from a shared web‐based learning environment?. Medical Education. 42(1). 27–33. 6 indexed citations
15.
Lam, Wayne, J M Kirk, N. J. Manning, et al.. (2005). Decreased cholesterol synthesis as a possible aetiological factor in malformations of Trisomy 18. European Journal of Medical Genetics. 49(2). 195–199. 13 indexed citations
16.
Gloyn, Anna L., C. Noordam, Michèl A.A.P. Willemsen, et al.. (2003). Insights Into the Biochemical and Genetic Basis of Glucokinase Activation From Naturally Occurring Hypoglycemia Mutations. Diabetes. 52(9). 2433–2440. 124 indexed citations
17.
Lam, Wayne, Izuho Hatada, Sachiko Oh‐ishi, et al.. (1999). Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation. Journal of Medical Genetics. 36(7). 518–523. 123 indexed citations
18.
Brewer, Carole, et al.. (1998). Beckwith-Wiedemann syndrome in a child with chromosome 18q deletion.. Journal of Medical Genetics. 35(2). 162–164. 6 indexed citations
19.
Lam, Wayne & E.R. Maher. (1998). Beckwith-Wiedemann syndrome. Current Paediatrics. 8(2). 117–120. 1 indexed citations
20.
Catchpoole, Daniel, Wayne Lam, I. Karen Temple, et al.. (1997). Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.. Journal of Medical Genetics. 34(5). 353–359. 73 indexed citations

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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