Piya Lahiry

990 total citations
16 papers, 642 citations indexed

About

Piya Lahiry is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Piya Lahiry has authored 16 papers receiving a total of 642 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Hematology. Recurrent topics in Piya Lahiry's work include Genetic Associations and Epidemiology (4 papers), Metabolism, Diabetes, and Cancer (3 papers) and Genomics and Rare Diseases (2 papers). Piya Lahiry is often cited by papers focused on Genetic Associations and Epidemiology (4 papers), Metabolism, Diabetes, and Cancer (3 papers) and Genomics and Rare Diseases (2 papers). Piya Lahiry collaborates with scholars based in Canada, United States and Denmark. Piya Lahiry's co-authors include Robert A. Hegele, Nicholas J. Schork, Ali Torkamani, Rebecca L. Pollex, Miguel A. Valvano, Cristina L. Marolda, Enrique D. Vinés, Tisha Joy, Matthew B. Lanktree and C. Anthony Rupar and has published in prestigious journals such as PLoS ONE, Nature Reviews Genetics and The American Journal of Human Genetics.

In The Last Decade

Piya Lahiry

15 papers receiving 624 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Piya Lahiry Canada	10	378	122	77	54	52	16	642
Zafar I. Randhawa United States	13	533 1.4×	82 0.7×	52 0.7×	17 0.3×	91 1.8×	22	919
Marcia L. Gaido United States	11	523 1.4×	69 0.6×	89 1.2×	15 0.3×	41 0.8×	14	919
Mario Torrado Spain	16	448 1.2×	85 0.7×	29 0.4×	31 0.6×	51 1.0×	23	712
Marie‐Elisabeth Forgue‐Lafitte France	13	280 0.7×	68 0.6×	151 2.0×	27 0.5×	52 1.0×	17	581
Jalal A. Jazayeri Australia	15	471 1.2×	84 0.7×	163 2.1×	21 0.4×	24 0.5×	24	779
J C Salomon France	18	387 1.0×	117 1.0×	151 2.0×	20 0.4×	54 1.0×	45	1.0k
Xingju Zhang China	17	998 2.6×	42 0.3×	133 1.7×	11 0.2×	69 1.3×	34	1.3k
Yoshio Kodera Japan	16	448 1.2×	64 0.5×	102 1.3×	22 0.4×	56 1.1×	33	768
D Bienz Switzerland	7	242 0.6×	208 1.7×	94 1.2×	29 0.5×	13 0.3×	8	564
Malcolm A. King Australia	15	468 1.2×	57 0.5×	148 1.9×	119 2.2×	27 0.5×	21	755

Countries citing papers authored by Piya Lahiry

Since Specialization

Citations

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

Fields of papers citing papers by Piya Lahiry

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Piya Lahiry

This figure shows the co-authorship network connecting the top 25 collaborators of Piya Lahiry. A scholar is included among the top collaborators of Piya Lahiry 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 Piya Lahiry. Piya Lahiry is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Chédeville, Gaëlle, Piya Lahiry, Jennifer J. Lee, et al.. (2023). Choosing Wisely: The Canadian Rheumatology Association Pediatric Committee’s List of Items Physicians and Patients Should Question. The Journal of Rheumatology. 50(12). 1610–1618.

Lahiry, Piya, Sergey Naumenko, Madeline Couse, et al.. (2022). Hemophagocytic Lymphohistiocytosis Gene Variants in Childhood-Onset Systemic Lupus Erythematosus With Macrophage Activation Syndrome. The Journal of Rheumatology. 49(10). 1146–1151. 1 indexed citations

Lahiry, Piya, Lemuel Racacho, Jian Wang, et al.. (2013). A mutation in the serine protease TMPRSS4 in a novel pediatric neurodegenerative disorder. Orphanet Journal of Rare Diseases. 8(1). 5 indexed citations

Farhan, Sali M.K., Jian Wang, John F. Robinson, et al.. (2013). Exome sequencing identifies NFS1 deficiency in a novel Fe‐S cluster disease, infantile mitochondrial complex II/III deficiency. Molecular Genetics & Genomic Medicine. 2(1). 73–80. 43 indexed citations

Lahiry, Piya, Leo J. Lee, Brendan J. Frey, et al.. (2011). Transcriptional Profiling of Endocrine Cerebro-Osteodysplasia Using Microarray and Next-Generation Sequencing. PLoS ONE. 6(9). e25400–e25400. 9 indexed citations

Lanktree, Matthew B., et al.. (2010). Phenomics: Expanding the Role of Clinical Evaluation in Genomic Studies. Journal of Investigative Medicine. 58(5). 700–706. 34 indexed citations

Lahiry, Piya, Jian Wang, J. F. Robinson, et al.. (2009). A Multiplex Human Syndrome Implicates a Key Role for Intestinal Cell Kinase in Development of Central Nervous, Skeletal, and Endocrine Systems. The American Journal of Human Genetics. 84(6). 822–822. 5 indexed citations

Lahiry, Piya, Jian Wang, John F. Robinson, et al.. (2009). A Multiplex Human Syndrome Implicates a Key Role for Intestinal Cell Kinase in Development of Central Nervous, Skeletal, and Endocrine Systems. The American Journal of Human Genetics. 84(2). 134–147. 53 indexed citations

Lahiry, Piya, Henian Cao, Matthew R. Ban, et al.. (2009). APOC1 T45S polymorphism is associated with reduced obesity indices and lower plasma concentrations of leptin and apolipoprotein C-I in aboriginal Canadians. Journal of Lipid Research. 51(4). 843–848. 13 indexed citations

10.

Lahiry, Piya, Ali Torkamani, Nicholas J. Schork, & Robert A. Hegele. (2009). Kinase mutations in human disease: interpreting genotype–phenotype relationships. Nature Reviews Genetics. 11(1). 60–74. 283 indexed citations

11.

Lahiry, Piya, et al.. (2009). Génétique du syndrome métabolique. 30(1). 25–32. 1 indexed citations

12.

Lahiry, Piya, Rebecca L. Pollex, & Robert A. Hegele. (2008). Uncloaking the Genetic Determinants of Metabolic Syndrome. Lifestyle Genomics. 1(3). 118–125. 13 indexed citations

13.

Hegele, R A, et al.. (2008). Understanding Beta-Thalassemia with Focus on the Indian Subcontinent and the Middle East. 2(1). 5–13. 19 indexed citations

14.

Joy, Tisha, Piya Lahiry, Rebecca L. Pollex, & Robert A. Hegele. (2008). Genetics of metabolic syndrome. Current Diabetes Reports. 8(2). 141–148. 64 indexed citations

15.

Lahiry, Piya, Matthew R. Ban, Rebecca L. Pollex, et al.. (2007). Common variants APOC3, APOA5, APOE and PON1 are associated with variation in plasma lipoprotein traits in Greenlanders. International Journal of Circumpolar Health. 66(5). 390–400. 12 indexed citations

16.

Marolda, Cristina L., et al.. (2006). Micromethods for the Characterization of Lipid A-Core and O-Antigen Lipopolysaccharide. Humana Press eBooks. 347. 237–252. 87 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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