Christina Lam

1.9k total citations
31 papers, 455 citations indexed

About

Christina Lam is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Christina Lam has authored 31 papers receiving a total of 455 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 7 papers in Physiology. Recurrent topics in Christina Lam's work include Glycosylation and Glycoproteins Research (14 papers), Metabolism and Genetic Disorders (7 papers) and Genomics and Rare Diseases (6 papers). Christina Lam is often cited by papers focused on Glycosylation and Glycoproteins Research (14 papers), Metabolism and Genetic Disorders (7 papers) and Genomics and Rare Diseases (6 papers). Christina Lam collaborates with scholars based in United States, Czechia and Canada. Christina Lam's co-authors include Irene J. Chang, Miao He, Lynne A. Wolfe, Derek A. Wong, Jenny Thies, Stephen Cederbaum, Kimiyo Raymond, Andrew C. Edmondson, Éva Morava and Angela Sun and has published in prestigious journals such as Scientific Reports, Human Molecular Genetics and The Journal of Pediatrics.

In The Last Decade

Christina Lam

28 papers receiving 452 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christina Lam United States 10 312 125 72 68 65 31 455
Maciej Adamowicz Poland 11 357 1.1× 108 0.9× 94 1.3× 103 1.5× 44 0.7× 14 471
Karin Huijben Netherlands 12 476 1.5× 121 1.0× 125 1.7× 171 2.5× 34 0.5× 18 594
Gülden Gökçay Türkiye 13 277 0.9× 56 0.4× 100 1.4× 20 0.3× 213 3.3× 30 492
Kayoko Yamashita Japan 11 267 0.9× 57 0.5× 40 0.6× 60 0.9× 26 0.4× 19 437
Vicki L. Nebes United States 12 188 0.6× 47 0.4× 111 1.5× 32 0.5× 47 0.7× 23 472
Anna M. Sokòl Germany 13 407 1.3× 29 0.2× 105 1.5× 40 0.6× 37 0.6× 24 597
Mei-Shiue Kuo France 8 371 1.2× 59 0.5× 37 0.5× 89 1.3× 7 0.1× 11 483
Elena Farmaki United States 13 200 0.6× 48 0.4× 27 0.4× 95 1.4× 30 0.5× 27 453
Tobias Ackermann Netherlands 9 310 1.0× 39 0.3× 52 0.7× 84 1.2× 13 0.2× 12 584
Valeriu Cebotaru United States 13 494 1.6× 215 1.7× 43 0.6× 15 0.2× 12 0.2× 20 694

Countries citing papers authored by Christina Lam

Since Specialization
Citations

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

Fields of papers citing papers by Christina Lam

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christina Lam

This figure shows the co-authorship network connecting the top 25 collaborators of Christina Lam. A scholar is included among the top collaborators of Christina 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 Christina Lam. Christina 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.
Hall, Patricia, Christina Lam, Lynne A. Wolfe, & Andrew C. Edmondson. (2025). Biochemical testing for congenital disorders of glycosylation: A technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 27(4). 101328–101328. 1 indexed citations
2.
Miyamoto, Ei, Christina Lam, Mingyao Liu, et al.. (2025). Permissive immunosuppression facilitates the expansion of ex vivo administered regulatory T cells in the lung allograft. Scientific Reports. 15(1). 22897–22897.
3.
Edmondson, Andrew C., et al.. (2025). Incidence and prevalence of phosphomannomutase 2-congenital disorder of glycosylation: Past, present, and future. Molecular Genetics and Metabolism. 146(1-2). 109188–109188.
4.
Scaglia, Fernando, et al.. (2025). Causes of mortality in the congenital disorders of glycosylation. Molecular Genetics and Metabolism. 144(3). 109052–109052.
5.
Lam, Christina, et al.. (2024). Neurodevelopmental profiles of 14 individuals with phosphomannomutase deficiency (PMM2‐CDG). Journal of Inherited Metabolic Disease. 48(1). e12782–e12782. 1 indexed citations
6.
Zemet, Roni, Andrew C. Edmondson, Justin H. Berger, et al.. (2024). Cardiomyopathy, an uncommon phenotype of congenital disorders of glycosylation: Recommendations for baseline screening and follow-up evaluation. Molecular Genetics and Metabolism. 142(4). 108513–108513. 4 indexed citations
7.
Dang, An, Irene J. Chang, Lynne A. Wolfe, et al.. (2023). Elevated oxysterol and N‐palmitoyl‐O‐phosphocholineserine levels in congenital disorders of glycosylation. Journal of Inherited Metabolic Disease. 46(2). 326–334. 4 indexed citations
8.
Watanabe, Tatsuaki, Christina Lam, Hisashi Oishi, et al.. (2023). Donor Batf3 inhibits murine lung allograft rejection and airway fibrosis. Mucosal Immunology. 16(2). 104–120. 4 indexed citations
9.
Ligezka, Anna N., Gina L. Mazza, Graeme Preston, et al.. (2023). Coagulation abnormalities in a prospective cohort of 50 patients with PMM2-congenital disorder of glycosylation. Molecular Genetics and Metabolism. 139(2). 107606–107606. 8 indexed citations
10.
Zhang, Tong, Christopher J. Collins, Jenny Thies, et al.. (2022). A rapid and non-invasive proteomic analysis using DBS and buccal swab for multiplexed second-tier screening of Pompe disease and Mucopolysaccharidosis type I. Molecular Genetics and Metabolism. 136(4). 296–305. 8 indexed citations
11.
Ligezka, Anna N., Carlota Pascoal, Vanessa dos Reis Ferreira, et al.. (2022). Patient-reported outcomes and quality of life in PMM2-CDG. Molecular Genetics and Metabolism. 136(2). 145–151. 14 indexed citations
12.
Čechová, Anna, Tomáš Honzík, Andrew C. Edmondson, et al.. (2021). Should patients with Phosphomannomutase 2-CDG (PMM2-CDG) be screened for adrenal insufficiency?. Molecular Genetics and Metabolism. 133(4). 397–399. 6 indexed citations
13.
Ng, Bobby G., Jennifer Friedman, Enikö K. Pivnick, et al.. (2021). Expanding the phenotype, genotype and biochemical knowledge of ALG3‐CDG. Journal of Inherited Metabolic Disease. 44(4). 987–1000. 9 indexed citations
14.
Raymond, Kimiyo, Hee Eun Lee, Lynne A. Wolfe, et al.. (2021). Liver manifestations in a cohort of 39 patients with congenital disorders of glycosylation: pin-pointing the characteristics of liver injury and proposing recommendations for follow-up. Orphanet Journal of Rare Diseases. 16(1). 20–20. 13 indexed citations
15.
Scott, Anna I., S.M. Sullivan, Irene J. Chang, et al.. (2020). Tutorial: Triheptanoin and Nutrition Management for Treatment of Long‐Chain Fatty Acid Oxidation Disorders. Journal of Parenteral and Enteral Nutrition. 45(2). 230–238. 14 indexed citations
16.
Hall, Patricia, Christina Lam, John Alexander, et al.. (2018). Urine oligosaccharide screening by MALDI-TOF for the identification of NGLY1 deficiency. Molecular Genetics and Metabolism. 124(1). 82–86. 28 indexed citations
17.
Starr, Michelle C., Irene J. Chang, Laura S. Finn, et al.. (2018). COQ2 nephropathy: a treatable cause of nephrotic syndrome in children. Pediatric Nephrology. 33(7). 1257–1261. 26 indexed citations
18.
Chang, Irene J., Miao He, & Christina Lam. (2018). Congenital disorders of glycosylation. Annals of Translational Medicine. 6(24). 477–477. 153 indexed citations
19.
Lam, Christina, Carla Ciccone, Heidi Dorward, et al.. (2014). Two novel compound heterozygous mutations in OPA3 in two siblings with OPA3-related 3-methylglutaconic aciduria. Molecular Genetics and Metabolism Reports. 1. 114–123. 6 indexed citations
20.
Lam, Christina, et al.. (2012). Peanut consumption increases levels of plasma very long chain fatty acids in humans. Molecular Genetics and Metabolism. 107(3). 620–622. 35 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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