Tammy S. Mah

2.2k total citations
18 papers, 1.4k citations indexed

About

Tammy S. Mah is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Tammy S. Mah has authored 18 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Ophthalmology and 8 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Tammy S. Mah's work include Retinal Diseases and Treatments (9 papers), Retinal Imaging and Analysis (6 papers) and Retinal Development and Disorders (6 papers). Tammy S. Mah is often cited by papers focused on Retinal Diseases and Treatments (9 papers), Retinal Imaging and Analysis (6 papers) and Retinal Development and Disorders (6 papers). Tammy S. Mah collaborates with scholars based in United States, Saudi Arabia and Germany. Tammy S. Mah's co-authors include Michael B. Gorin, Daniel E. Weeks, Yvette P. Conley, Robert E. Ferrell, Jóhanna Jakobsdóttir, F. Yesim Demirci, Brian W. Rigatti, R E Ferrell, T. Otis Paul and Hui‐Ju Tsai and has published in prestigious journals such as Genome Research, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Tammy S. Mah

18 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tammy S. Mah United States 15 954 787 622 183 124 18 1.4k
Monica A. De La Paz United States 14 429 0.4× 299 0.4× 233 0.4× 40 0.2× 25 0.2× 19 606
Maria M Campos United States 15 293 0.3× 409 0.5× 107 0.2× 67 0.4× 82 0.7× 33 639
Heidi Roehrich United States 15 342 0.4× 443 0.6× 95 0.2× 23 0.1× 127 1.0× 29 752
Una Kelly United States 13 436 0.5× 404 0.5× 190 0.3× 54 0.3× 180 1.5× 20 783
Naomichi Katai Japan 15 341 0.4× 446 0.6× 101 0.2× 16 0.1× 38 0.3× 28 792
Sindhu Saraswathy United States 16 413 0.4× 260 0.3× 143 0.2× 15 0.1× 111 0.9× 36 666
Altan Atakan Özcan Türkiye 10 496 0.5× 168 0.2× 285 0.5× 33 0.2× 58 0.5× 36 744
Edward A. Felinski United States 7 251 0.3× 337 0.4× 140 0.2× 34 0.2× 43 0.3× 7 732
Andrew Orr Canada 12 95 0.1× 348 0.4× 79 0.1× 226 1.2× 16 0.1× 17 735
Gaël Cagnone Canada 17 124 0.1× 508 0.6× 83 0.1× 121 0.7× 62 0.5× 37 916

Countries citing papers authored by Tammy S. Mah

Since Specialization
Citations

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

Fields of papers citing papers by Tammy S. Mah

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tammy S. Mah. 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 Tammy S. Mah. The network helps show where Tammy S. Mah may publish in the future.

Co-authorship network of co-authors of Tammy S. Mah

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

All Works

18 of 18 papers shown
1.
Conley, Yvette P., Jóhanna Jakobsdóttir, Tammy S. Mah, et al.. (2007). CFH, ELOVL4, PLEKHA1, and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses. American Journal of Ophthalmology. 143(4). 732–733. 6 indexed citations
2.
Conley, Yvette P., Jóhanna Jakobsdóttir, Tammy S. Mah, et al.. (2006). CFH, ELOVL4, PLEKHA1 and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses. Human Molecular Genetics. 15(21). 3206–3218. 121 indexed citations
3.
Demirci, F. Yesim, et al.. (2006). Proximal renal tubular acidosis and ocular pathology: a novel missense mutation in the gene (SLC4A4) for sodium bicarbonate cotransporter protein (NBCe1).. PubMed. 12. 324–30. 80 indexed citations
4.
Demirci, F. Yesim, Nisha Gupta, Brian W. Rigatti, et al.. (2005). Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15. American Journal of Ophthalmology. 139(2). 386–388. 16 indexed citations
5.
Jakobsdóttir, Jóhanna, Yvette P. Conley, Daniel E. Weeks, et al.. (2005). Susceptibility Genes for Age-Related Maculopathy on Chromosome 10q26. The American Journal of Human Genetics. 77(3). 389–407. 374 indexed citations
6.
Demirci, F. Yesim, Brian W. Rigatti, Tammy S. Mah, & Michael B. Gorin. (2005). A Novel RPGR Exon ORF15 Mutation in a Family With X-linked Retinitis Pigmentosa and Coats’-like Exudative Vasculopathy. American Journal of Ophthalmology. 141(1). 208–210. 20 indexed citations
7.
Conley, Yvette P., Anbupalam Thalamuthu, Jóhanna Jakobsdóttir, et al.. (2005). Candidate gene analysis suggests a role for fatty acid biosynthesis and regulation of the complement system in the etiology of age-related maculopathy. Human Molecular Genetics. 14(14). 1991–2002. 123 indexed citations
8.
Demirci, F. Yesim, et al.. (2004). A presumed missense mutation of RPGR causes abnormal RNA splicing with exon skipping. American Journal of Ophthalmology. 138(3). 504–505. 12 indexed citations
9.
Weeks, Daniel E., Yvette P. Conley, Hui‐Ju Tsai, et al.. (2004). Age-Related Maculopathy: A Genomewide Scan with Continued Evidence of Susceptibility Loci within the 1q31, 10q26, and 17q25 Regions. The American Journal of Human Genetics. 75(2). 174–189. 142 indexed citations
10.
Demirci, F. Yesim, Brian W. Rigatti, Tammy S. Mah, & Michael B. Gorin. (2004). A novel compound heterozygous mutation in the cellular retinaldehyde-binding protein gene (RLBP1) in a patient with retinitis punctata albescens. American Journal of Ophthalmology. 138(1). 171–173. 18 indexed citations
11.
Demirci, F. Yesim, Brian W. Rigatti, Gaiping Wen, et al.. (2002). X-Linked Cone-Rod Dystrophy (Locus COD1): Identification of Mutations in RPGR Exon ORF15. The American Journal of Human Genetics. 70(4). 1049–1053. 138 indexed citations
12.
Gordon, Y. Jerold, et al.. (2002). Fluorescein-Potentiated Argon Laser Therapy Improves Symptoms and Appearance of Corneal Neovascularization. Cornea. 21(8). 770–773. 21 indexed citations
13.
Weeks, Daniel E., Yvette P. Conley, Robert E. Ferrell, Tammy S. Mah, & Michael B. Gorin. (2002). A Tale of Two Genotypes: Consistency between Two High-Throughput Genotyping Centers. Genome Research. 12(3). 430–435. 39 indexed citations
14.
Weeks, Daniel E., Yvette P. Conley, Hui‐Ju Tsai, et al.. (2001). Age-related maculopathy: an expanded genome-wide scan with evidence of susceptibility loci within the 1q31 and 17q25 regions. American Journal of Ophthalmology. 132(5). 682–692. 102 indexed citations
15.
Conley, Yvette P., Tammy S. Mah, Annahita Keravala, et al.. (2000). A Juvenile-Onset, Progressive Cataract Locus on Chromosome 3q21-q22 Is Associated with a Missense Mutation in the Beaded Filament Structural Protein–2. The American Journal of Human Genetics. 66(4). 1426–1431. 120 indexed citations
16.
Hardcastle, Alison J., Dawn L. Thiselton, Ilaria Zito, et al.. (2000). Evidence for a new locus for X-linked retinitis pigmentosa (RP23).. PubMed. 41(8). 2080–6. 42 indexed citations
17.
Mah, Tammy S., et al.. (1998). A practice-based survey of familial age-related maculopathy. Ophthalmic Genetics. 19(1). 19–26. 6 indexed citations
18.
Seymour, Albert, Jeffrey R. O’Connell, Tammy S. Mah, et al.. (1998). Linkage Analysis of X-linked Cone-Rod Dystrophy: Localization to Xp11.4 and Definition of a Locus Distinct from RP2 and RP3. The American Journal of Human Genetics. 62(1). 122–129. 15 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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