Sylvia Mann Au

506 total citations
8 papers, 125 citations indexed

About

Sylvia Mann Au is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Clinical Biochemistry. According to data from OpenAlex, Sylvia Mann Au has authored 8 papers receiving a total of 125 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pediatrics, Perinatology and Child Health, 4 papers in Genetics and 3 papers in Clinical Biochemistry. Recurrent topics in Sylvia Mann Au's work include Prenatal Screening and Diagnostics (3 papers), BRCA gene mutations in cancer (3 papers) and Neonatal Health and Biochemistry (3 papers). Sylvia Mann Au is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), BRCA gene mutations in cancer (3 papers) and Neonatal Health and Biochemistry (3 papers). Sylvia Mann Au collaborates with scholars based in United States. Sylvia Mann Au's co-authors include Lisa Feuchtbaum, Sverre Vedal, Cary O. Harding, Bruce A. Barshop, Fred Lorey, José E. Abdenur, J. Lawrence Merritt, David E. Sesser, Kerry Silvey and Kirsty McWalter and has published in prestigious journals such as American Journal of Preventive Medicine, Genetics in Medicine and Molecular Genetics and Metabolism.

In The Last Decade

Sylvia Mann Au

8 papers receiving 115 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sylvia Mann Au United States	5	64	54	50	32	22	8	125
Natasha Bonhomme United States	7	78 1.2×	87 1.6×	98 2.0×	33 1.0×	54 2.5×	22	228
Kylie Tingley Canada	5	33 0.5×	17 0.3×	40 0.8×	23 0.7×	8 0.4×	11	110
Melanie Downing United Kingdom	5	64 1.0×	55 1.0×	32 0.6×	32 1.0×	7 0.3×	7	125
Laura Irving United Kingdom	4	47 0.7×	19 0.4×	10 0.2×	87 2.7×	16 0.7×	5	115
Gemma R. Brett Australia	7	8 0.1×	34 0.6×	126 2.5×	23 0.7×	42 1.9×	10	163
Sara Caylor United States	4	16 0.3×	34 0.6×	109 2.2×	44 1.4×	13 0.6×	4	139
Aida I. Al Aqeel Saudi Arabia	3	5 0.1×	19 0.4×	59 1.2×	40 1.3×	16 0.7×	3	97
Tafadzwa Machipisa South Africa	5	21 0.3×	8 0.1×	63 1.3×	71 2.2×	17 0.8×	10	162
Jessie H. Conta United States	7	10 0.2×	33 0.6×	119 2.4×	28 0.9×	61 2.8×	14	190
Chloe Mighton Canada	10	6 0.1×	36 0.7×	252 5.0×	64 2.0×	49 2.2×	30	318

Countries citing papers authored by Sylvia Mann Au

Since Specialization

Citations

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

Fields of papers citing papers by Sylvia Mann Au

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sylvia Mann Au. 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 Sylvia Mann Au. The network helps show where Sylvia Mann Au may publish in the future.

Co-authorship network of co-authors of Sylvia Mann Au

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

All Works

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8 of 8 papers shown

1.

Merritt, J. Lawrence, Sverre Vedal, José E. Abdenur, et al.. (2014). Infants suspected to have very-long chain acyl-CoA dehydrogenase deficiency from newborn screening. Molecular Genetics and Metabolism. 111(4). 484–492. 43 indexed citations

2.

McWalter, Kirsty, et al.. (2013). Provision of Genetics Services on Guam. Journal of Genetic Counseling. 22(6). 885–889. 2 indexed citations

3.

Guzauskas, Gregory F., et al.. (2012). Stakeholder perspectives on decision-analytic modeling frameworks to assess genetic services policy. Genetics in Medicine. 15(1). 84–87. 2 indexed citations

4.

McWalter, Kirsty, et al.. (2011). Hemoglobinopathy Newborn Screening Knowledge of Physicians. American Journal of Preventive Medicine. 41(6). S384–S389. 5 indexed citations

5.

Au, Sylvia Mann, et al.. (2010). Parental Attitudes toward Ethical and Social Issues Surrounding the Expansion of Newborn Screening Using New Technologies. Public Health Genomics. 14(4-5). 298–306. 51 indexed citations

6.

Silvey, Kerry, et al.. (2009). Outcomes of genetics services: Creating an inclusive definition and outcomes menu for public health and clinical genetics services. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 151C(3). 207–213. 13 indexed citations

7.

Au, Sylvia Mann, et al.. (2009). Tell Us What You Need: Health Care Perspectives of Guam Families with Genetic Diagnoses. 2(1). 46–59. 1 indexed citations

8.

Au, Sylvia Mann, et al.. (2005). The obstetrician's role in newborn metabolic screening: a physician survey.. PubMed. 64(9). 239–43, 253. 8 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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