Thomas A. Maher

928 total citations
23 papers, 586 citations indexed

About

Thomas A. Maher is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Thomas A. Maher has authored 23 papers receiving a total of 586 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Thomas A. Maher's work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Thomas A. Maher is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Thomas A. Maher collaborates with scholars based in United States, Uruguay and Canada. Thomas A. Maher's co-authors include Jeff M. Milunsky, Aubrey Milunsky, Geping Zhao, Robert D. Oates, Virginia V. Michels, Masamichi Ito, Aı̈da Metzenberg, Michael Dean, Bernard Gerrard and Arturo Anguiano and has published in prestigious journals such as PEDIATRICS, International Journal of Molecular Sciences and CHEST Journal.

In The Last Decade

Thomas A. Maher

22 papers receiving 570 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas A. Maher United States 13 270 147 137 112 61 23 586
Valère Cacheux France 10 415 1.5× 417 2.8× 166 1.2× 128 1.1× 53 0.9× 12 847
Edmond G. Lemire Canada 14 240 0.9× 202 1.4× 142 1.0× 67 0.6× 26 0.4× 42 616
Elisabetta Lapi Italy 18 534 2.0× 477 3.2× 61 0.4× 70 0.6× 54 0.9× 48 957
Dilek Aktaş Türkiye 17 423 1.6× 455 3.1× 43 0.3× 106 0.9× 42 0.7× 68 873
Lakshmi Mehta United States 16 403 1.5× 348 2.4× 44 0.3× 96 0.9× 34 0.6× 46 754
Olaf Rittinger Austria 17 433 1.6× 384 2.6× 47 0.3× 66 0.6× 24 0.4× 40 785
Junko Kanno Japan 12 264 1.0× 188 1.3× 139 1.0× 39 0.3× 25 0.4× 33 850
Joy B. Redman United States 17 301 1.1× 203 1.4× 290 2.1× 31 0.3× 18 0.3× 27 781
Nancy J. Charest United States 8 215 0.8× 133 0.9× 88 0.6× 38 0.3× 14 0.2× 9 616

Countries citing papers authored by Thomas A. Maher

Since Specialization
Citations

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

Fields of papers citing papers by Thomas A. Maher

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas A. Maher. 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 Thomas A. Maher. The network helps show where Thomas A. Maher may publish in the future.

Co-authorship network of co-authors of Thomas A. Maher

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas A. Maher. A scholar is included among the top collaborators of Thomas A. Maher 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 Thomas A. Maher. Thomas A. Maher 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.
Alekseyev, Yuriy O., Roghayeh Fazeli, Yang Shi, et al.. (2018). A Next-Generation Sequencing Primer—How Does It Work and What Can It Do?. Academic Pathology. 5. 1532766649–1532766649. 53 indexed citations
2.
Maher, Thomas A., Raveen Basran, Aubrey Milunsky, et al.. (2011). Fraternal twins with Aarskog–Scott syndrome due to maternal germline mosaicism. American Journal of Medical Genetics Part A. 155(8). 1987–1990. 7 indexed citations
3.
4.
Milunsky, Aubrey, et al.. (2009). Prenatal molecular diagnosis of tuberous sclerosis complex. American Journal of Obstetrics and Gynecology. 200(3). 321.e1–321.e6. 12 indexed citations
5.
6.
Milunsky, Jeff M., Thomas A. Maher, M. Ito, & Aubrey Milunsky. (2007). The Value of MLPA in Waardenburg Syndrome. Genetic Testing. 11(2). 179–182. 23 indexed citations
7.
Leon, Eyby, et al.. (2007). Pallister–Killian syndrome: tetrasomy of 12pter→12p11.22 in a boy with an analphoid, inverted duplicated marker chromosome. Clinical Genetics. 72(5). 434–440. 5 indexed citations
8.
Zhao, Geping, et al.. (2006). LADD syndrome is caused byFGF10mutations. Clinical Genetics. 69(4). 349–354. 110 indexed citations
9.
Shim, Sung Han, Masamichi Ito, Thomas A. Maher, & Aubrey Milunsky. (2005). Gene Sequencing in Neonates and Infants with the Long QT Syndrome. Genetic Testing. 9(4). 281–284. 18 indexed citations
10.
11.
Maher, Thomas A., et al.. (2003). XL PCR for the detection of large trinucleotide expansions in juvenile Huntington's disease. Clinical Genetics. 64(1). 70–73. 28 indexed citations
12.
Milunsky, Jeff M., Thomas A. Maher, & Aı̈da Metzenberg. (2003). Response to correspondence from Happle—“Hypomorphic alleles within the EBP gene cause a phenotype quite different from conradi‐hunermann‐Happle”. American Journal of Medical Genetics Part A. 122A(3). 280–280. 1 indexed citations
13.
Milunsky, Jeff M., Thomas A. Maher, & Aı̈da Metzenberg. (2002). Molecular, biochemical, and phenotypic analysis of a hemizygous male with a severe atypical phenotype for X‐linked dominant Conradi‐Hunermann‐Happle syndrome and a mutation in EBP. American Journal of Medical Genetics Part A. 116A(3). 249–254. 32 indexed citations
14.
Milunsky, Jeff M., et al.. (2001). Mutation Analysis in Rett Syndrome. Genetic Testing. 5(4). 321–325. 18 indexed citations
15.
Milunsky, Jeff M., Thomas A. Maher, Virginia V. Michels, & Aubrey Milunsky. (2001). Novel mutations and the emergence of a common mutation in theSDHD gene causing familial paraganglioma. American Journal of Medical Genetics. 100(4). 311–314. 61 indexed citations
16.
Lebo, Roger V., et al.. (2001). Highly Polymorphic Short Tandem Repeat Analyses Clarify Complex Molecular Test Results. Diagnostic Molecular Pathology. 10(3). 179–189. 1 indexed citations
17.
Milunsky, Jeff M., et al.. (2000). Connexin-26 Gene Analysis in Hearing-Impaired Newborns. Genetic Testing. 4(4). 345–349. 17 indexed citations
18.
McCallum, Theresa J., et al.. (2000). Fertility in Men With Cystic Fibrosis. CHEST Journal. 118(4). 1059–1062. 61 indexed citations
19.
Milunsky, Jeff M., Thomas A. Maher, Roger V. Lebo, & Aubrey Milunsky. (1998). Prenatal Diagnosis for Schmid Metaphyseal Chondrodysplasia in Twins. Fetal Diagnosis and Therapy. 13(3). 167–168.
20.
Milunsky, Aubrey, et al.. (1991). Prenatal diagnosis of myotonic muscular dystrophy with linked deoxyribonucleic acid probes. American Journal of Obstetrics and Gynecology. 164(3). 751–755. 1 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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