Kathleen Rao

503 total citations
9 papers, 312 citations indexed

About

Kathleen Rao is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Kathleen Rao has authored 9 papers receiving a total of 312 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Genetics. Recurrent topics in Kathleen Rao's work include Genetics and Neurodevelopmental Disorders (2 papers), Hereditary Neurological Disorders (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Kathleen Rao is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Hereditary Neurological Disorders (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Kathleen Rao collaborates with scholars based in United States, India and United Kingdom. Kathleen Rao's co-authors include Alastair J. Martin, Daniel H. Geschwind, Cynthia M. Powell, Edwin H. Cook, Jason S. Simon, S.M. Totey, Deepak Sharma, Jack Tarleton, Arthur S. Aylsworth and Kathleen Kaiser‐Rogers and has published in prestigious journals such as Blood, Human Molecular Genetics and Genomics.

In The Last Decade

Kathleen Rao

9 papers receiving 292 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kathleen Rao United States 7 203 156 65 29 24 9 312
Sarah Morse United States 7 114 0.6× 38 0.2× 27 0.4× 41 1.4× 28 1.2× 15 261
Andreas Th. Müller Austria 9 126 0.6× 56 0.4× 21 0.3× 5 0.2× 10 0.4× 30 290
Jenny Morton United Kingdom 6 90 0.4× 122 0.8× 68 1.0× 12 0.4× 9 0.4× 8 236
W. J. Kimberling United States 8 126 0.6× 94 0.6× 50 0.8× 20 0.7× 12 0.5× 19 374
Valerie E. Vancollie United Kingdom 8 162 0.8× 60 0.4× 19 0.3× 5 0.2× 12 0.5× 12 278
Mark A. Brimble United States 8 168 0.8× 82 0.5× 25 0.4× 4 0.1× 13 0.5× 19 250
Tania Radziewic Australia 6 276 1.4× 189 1.2× 98 1.5× 4 0.1× 24 1.0× 8 378
Nathalie Fieremans Belgium 9 154 0.8× 162 1.0× 28 0.4× 10 0.3× 11 0.5× 10 264
A N Mhatre United States 7 261 1.3× 160 1.0× 50 0.8× 4 0.1× 75 3.1× 12 441
Jin Jea Sung South Korea 8 461 2.3× 174 1.1× 46 0.7× 59 2.0× 36 1.5× 13 513

Countries citing papers authored by Kathleen Rao

Since Specialization
Citations

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

Fields of papers citing papers by Kathleen Rao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kathleen Rao

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

All Works

9 of 9 papers shown
1.
Blatt, Julie, et al.. (2010). Isolated Central Nervous System Relapse in an Adolescent With Acute Myelomonocytic Leukemia, Charcot Marie Tooth Syndrome, and Paraneoplastic Autoantibody. Journal of Pediatric Hematology/Oncology. 32(7). 571–573. 2 indexed citations
3.
Martin, Alastair J., Jason S. Simon, Cynthia M. Powell, et al.. (2007). Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(7). 869–876. 162 indexed citations
5.
Sharma, Deepak, Kathleen Rao, & S.M. Totey. (2000). Measurement of within and between population genetic variability in quails. British Poultry Science. 41(1). 29–32. 32 indexed citations
6.
Woodward, Karen, Rodger Palmer, Kathleen Rao, & Sue Malcolm. (1999). Prenatal diagnosis by FISH in a family with Pelizaeus–Merzbacher disease caused by duplication of the PLP gene. Prenatal Diagnosis. 19(3). 266–268. 14 indexed citations
7.
Gu, Jing, et al.. (1994). Assignment of the Human Type I IMP Dehydrogenase Gene (IMPDH1) to Chromosome 7q31.3-q32. Genomics. 24(1). 179–181. 16 indexed citations
8.
Tarleton, Jack, et al.. (1993). An Extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype. Human Molecular Genetics. 2(11). 1973–1974. 58 indexed citations
9.
Ayscue, Lanier H., Dennis W. Ross, Howard Ozer, et al.. (1990). Bcr/abl Recombinant DNA Analysis Versus Karyotype in the Diagnosis and Therapeutic Monitoring of Chronic Myeloid Leukemia. American Journal of Clinical Pathology. 94(4). 404–409. 16 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026