Regan Klatt

869 total citations
10 papers, 155 citations indexed

About

Regan Klatt is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Regan Klatt has authored 10 papers receiving a total of 155 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Surgery and 3 papers in Genetics. Recurrent topics in Regan Klatt's work include Retinal Development and Disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Lysosomal Storage Disorders Research (2 papers). Regan Klatt is often cited by papers focused on Retinal Development and Disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Lysosomal Storage Disorders Research (2 papers). Regan Klatt collaborates with scholars based in Canada, United States and Ireland. Regan Klatt's co-authors include Marie E. Faughnan, Joel Katz, Joe T.R. Clarke, Leona Fishman, Cheryl Cytrynbaum, Adam C. Smith, Roberto Mendoza‐Londono, Jack Johnson, Peter N. Ray and Rosanna Weksberg and has published in prestigious journals such as European Respiratory Journal, American Journal of Medical Genetics Part A and Documenta Ophthalmologica.

In The Last Decade

Regan Klatt

9 papers receiving 153 citations

Peers

Countries citing papers authored by Regan Klatt

Since Specialization

Citations

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

Fields of papers citing papers by Regan Klatt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Regan Klatt

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	Insights into the effects of subretinal voretigene neparvovec-rzyl in RPE65-associated Leber congenital amaurosis 2025 ·Canadian Journal of Ophthalmology ·(unknown), (unknown), Peter J. Kertes, Rajeev H. Muni, (unknown), Gregory Costain, Adrien E. Schramm, H. Robson MacDonald, Regan Klatt, Ajoy Vincent, Elise Héon	1
2	Rod bipolar cell dysfunction in POLG retinopathy 2020 ·Documenta Ophthalmologica ·(unknown), (unknown), (unknown), Regan Klatt, Neal Sondheimer, Ajoy Vincent	0
3	Expanding the clinical spectrum of ocular anomalies in Noonan syndrome: Axenfeld‐anomaly in a child with PTPN11 mutation 2014 ·American Journal of Medical Genetics Part A ·Andrea Guerin, Joyce So, Kamiar Mireskandari, (unknown), (unknown), Regan Klatt, Julie Richer	5
4	Middle and inner ear malformations in mutation‐proven branchio‐oculo‐facial (BOF) syndrome: Case series and review of the literature 2012 ·American Journal of Medical Genetics Part A ·Melissa T. Carter, Susan Blasér, Blake C. Papsin, Wendy S. Meschino, William Reardon, Regan Klatt, Riyana Babul‐Hirji, Jeff M. Milunsky, David Chitayat	3
5	Idiopathic pulmonary arteriovenous malformations: clinical and imaging characteristics 2010 ·European Respiratory Journal ·(unknown), (unknown), Regan Klatt, Marie E. Faughnan	45
6	Molecular breakpoint mapping of 6q11‐q14 interstitial deletions in seven patients 2009 ·American Journal of Medical Genetics Part A ·Jia‐Chi Wang, (unknown), Brenda Lomax, Lesley Turner, Mary Shago, Ahmad S. Teebi, Regan Klatt, Patrick MacLeod, Siu‐Li Yong, Małgorzata J.M. Nowaczyk, Patrice Eydoux	6
7	Disease Rarity, Carrier Status, and Gender: A Triple Disadvantage for Women with Fabry Disease 2008 ·Journal of Genetic Counseling ·(unknown), Regan Klatt, (unknown), Joe T.R. Clarke, Joel Katz	23
8	Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification 2007 ·American Journal of Medical Genetics Part A ·(unknown), Berivan Baskin, Adam C. Smith, Andrea Shugar, Cheryl Cytrynbaum, Leona Fishman, Roberto Mendoza‐Londono, Regan Klatt, (unknown), Peter N. Ray, Rosanna Weksberg	39
9	A Survey of the Pain Experienced by Males and Females with Fabry Disease 2006 ·Pain Research and Management ·(unknown), Regan Klatt, Jack Johnson, Joe T.R. Clarke, Joel Katz	22
10	Remifentanil-Propofol- Anästhesie bei Bandscheibenoperationen: ein Vergleich mit einer Desfluran-N 2 O- Inhalationsanästhesie 1998 ·Der Anaesthesist ·U. Grundmann, Anne Katrin Risch, S. Kleinschmidt, Regan Klatt, R. Larsen	11

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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