Riyana Babul

451 total citations
12 papers, 252 citations indexed

About

Riyana Babul is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Riyana Babul has authored 12 papers receiving a total of 252 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Pediatrics, Perinatology and Child Health and 4 papers in Genetics. Recurrent topics in Riyana Babul's work include Prenatal Screening and Diagnostics (5 papers), Genetic Neurodegenerative Diseases (3 papers) and Mitochondrial Function and Pathology (2 papers). Riyana Babul is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genetic Neurodegenerative Diseases (3 papers) and Mitochondrial Function and Pathology (2 papers). Riyana Babul collaborates with scholars based in Canada and United States. Riyana Babul's co-authors include David Chitayat, Ikuko Teshima, Maurice Bloch, B Kremer, Jane Theilmann, Meredith M. Silver, Michael R. Hayden, S Wiggins, Shelin Adam and Marlene J. Huggins and has published in prestigious journals such as JAMA, American Journal of Medical Genetics and Journal of Genetic Counseling.

In The Last Decade

Riyana Babul

12 papers receiving 248 citations

Peers

Riyana Babul

GENET

MB

PPCH

CMN

GENET

Weiyi Mu United States

Atsushi Ieshima Japan

Lailá Bastaki Kuwait

Mélanie Fradin France

Emma S. James United States

Suzanne Braga Switzerland

Asım Cenani Türkiye

Tamar Schwartz Israel

Lorraine Gaunt United Kingdom

Valerie Drasinover Israel

Weiyi Mu United States

Riyana Babul

148 ×1.2

GENET

141 ×1.4

MB

35 ×0.6

PPCH

19 ×0.4

CMN

26 ×0.8

GENET

Citations per year, relative to Riyana Babul Riyana Babul (= 1×) peers Weiyi Mu

Countries citing papers authored by Riyana Babul

Since Specialization

Citations

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

Fields of papers citing papers by Riyana Babul

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Riyana Babul

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

All Works

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12 of 12 papers shown

1.

Chitayat, David, Ants Toi, Riyana Babul, et al.. (1997). Omphalocele in Miller-Dieker syndrome: Expanding the phenotype. American Journal of Medical Genetics. 69(3). 293–298. 21 indexed citations

2.

Chitayat, David, et al.. (1997). Limb defects in homozygous α-thalassemia: Report of three cases. American Journal of Medical Genetics. 68(2). 162–167. 22 indexed citations

3.

Lopes‐Cendes, Íscia, Isabel Silveira, Patrı́cia Maciel, et al.. (1996). Limits of Clinical Assessment in the Accurate Diagnosis of Machado-Joseph Disease. Archives of Neurology. 53(11). 1168–1174. 20 indexed citations

4.

Chitayat, David, Riyana Babul, Meredith M. Silver, et al.. (1996). Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27→qter)]. American Journal of Medical Genetics. 61(1). 45–48. 23 indexed citations

5.

Allingham‐Hawkins, Diane, Charlotte A. Brown, Riyana Babul, et al.. (1996). Tissue-specific methylation differences and cognitive function in fragile X premutation females. American Journal of Medical Genetics. 64(2). 329–333. 27 indexed citations

6.

Allingham‐Hawkins, Diane, Charlotte A. Brown, Riyana Babul, et al.. (1996). Tissue‐specific methylation differences and cognitive function in fragile X premutation females. American Journal of Medical Genetics. 64(2). 329–333. 1 indexed citations

7.

Fitzpatrick, Jennifer, et al.. (1996). Counseling and screening for cystic fibrosis in patients with congenital bilateral absence of the vas deferens: Patient perceptions. Journal of Genetic Counseling. 5(1). 1–15. 1 indexed citations

8.

Chitayat, David, Rogelio H.A. Ruvalcaba, Riyana Babul, et al.. (1995). Syndrome of proximal interstitial deletion 4p15: Report of three cases and review of the literature. American Journal of Medical Genetics. 55(2). 147–154. 28 indexed citations

9.

Chitayat, David, Ants Toi, Riyana Babul, et al.. (1995). Prenatal diagnosis of retinal nonattachment in the Walker‐Warburg syndrome. American Journal of Medical Genetics. 56(4). 351–358. 18 indexed citations

10.

Campeau, Eric, David Watkins, Guy A. Rouleau, et al.. (1995). Linkage analysis of the nail-patella syndrome.. PubMed. 56(1). 243–7. 20 indexed citations

11.

Babul, Riyana. (1993). Attitudes Toward Direct Predictive Testing for the Huntington Disease Gene. JAMA. 270(19). 2321–2321. 16 indexed citations

12.

Babul, Riyana, Shelin Adam, B Kremer, et al.. (1993). Attitudes toward direct predictive testing for the Huntington disease gene. Relevance for other adult-onset disorders. The Canadian Collaborative Group on Predictive Testing for Huntington Disease.. PubMed. 270(19). 2321–5. 55 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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