Margaret Drummond‐Borg

886 total citations
17 papers, 475 citations indexed

About

Margaret Drummond‐Borg is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Surgery. According to data from OpenAlex, Margaret Drummond‐Borg has authored 17 papers receiving a total of 475 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 4 papers in Genetics and 3 papers in Surgery. Recurrent topics in Margaret Drummond‐Borg's work include Prenatal Screening and Diagnostics (5 papers), Neonatal Health and Biochemistry (3 papers) and Metabolism and Genetic Disorders (3 papers). Margaret Drummond‐Borg is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Neonatal Health and Biochemistry (3 papers) and Metabolism and Genetic Disorders (3 papers). Margaret Drummond‐Borg collaborates with scholars based in United States. Margaret Drummond‐Borg's co-authors include S S Deeb, Arno G. Motulsky, Cynthia F. Hinton, Katharine B. Harris, Bradford L. Therrell, Roger B. Eaton, Fred Lorey, Kenneth A. Pass, Raye Lynn Alford and Michael E. Speer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and PEDIATRICS.

In The Last Decade

Margaret Drummond‐Borg

14 papers receiving 468 citations

Peers

Margaret Drummond‐Borg

EDM

PPCH

PRM

GENET

Rebecca Perry United Kingdom

John F. Connelly Australia

Waleed Altwaijri Saudi Arabia

W Schönberger Germany

Gerald J. Bargman United States

Alfonso Verdú Spain

Ella Sugo Australia

Julia Rohayem Germany

Yoshihito Inoue Japan

T. Criscuolo Italy

Rebecca Perry United Kingdom

Margaret Drummond‐Borg

273 ×1.3

EDM

196 ×1.1

87 ×0.5

PPCH

68 ×0.7

PRM

151 ×2.2

GENET

Citations per year, relative to Margaret Drummond‐Borg Margaret Drummond‐Borg (= 1×) peers Rebecca Perry

Countries citing papers authored by Margaret Drummond‐Borg

Since Specialization

Citations

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

Fields of papers citing papers by Margaret Drummond‐Borg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Margaret Drummond‐Borg. 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 Margaret Drummond‐Borg. The network helps show where Margaret Drummond‐Borg may publish in the future.

Co-authorship network of co-authors of Margaret Drummond‐Borg

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

All Works

Sort: Min cites: Since: Top N: Style:

17 of 17 papers shown

Benjamin, Renata H., Joanne Nguyen, Margaret Drummond‐Borg, et al.. (2024). Classification of isolated versus multiple birth defects: An automated process for population‐based registries. American Journal of Medical Genetics Part A. 194(10). e63714–e63714.

Lupo, Philip J., Natalie P. Archer, Lisa K. Marengo, et al.. (2024). Newborn screening analytes and structural birth defects among 27,000 newborns. PLoS ONE. 19(7). e0304238–e0304238. 1 indexed citations

Howell, R. J. S., Lisa K. Marengo, Andrew Dixon, et al.. (2024). Epidemiology of Macrocephaly in the Texas Birth Defects Registry, 1999–2019. Birth Defects Research. 116(11). e2415–e2415.

Langlois, Peter H., Lisa K. Marengo, Philip J. Lupo, et al.. (2022). Evaluating the proportion of isolated cases among a spectrum of birth defects in a population‐based registry. Birth Defects Research. 115(1). 21–25. 7 indexed citations

Benjamin, Renata H., Laura E. Mitchell, Angela E. Scheuerle, et al.. (2022). Identifying syndromes in studies of structural birth defects: Guidance on classification and evaluation of potential impact. American Journal of Medical Genetics Part A. 191(1). 190–204. 5 indexed citations

Marengo, Lisa K., et al.. (2022). Survival of infants and children born with severe microcephaly, Texas, 1999–2015. Birth Defects Research. 115(1). 26–42. 1 indexed citations

Canfield, Mark A., et al.. (2022). Connecting children with birth defects to health and social service programs: A collaboration between the Texas Birth Defects Registry and agency social workers. Birth Defects Research. 115(1). 110–119.

Parks, John S., Michelle Lin, Scott D. Grosse, et al.. (2010). The Impact of Transient Hypothyroidism on the Increasing Rate of Congenital Hypothyroidism in the United States. PEDIATRICS. 125(Supplement_2). S54–S63. 85 indexed citations

Hinton, Cynthia F., Katharine B. Harris, Margaret Drummond‐Borg, et al.. (2010). Trends in Incidence Rates of Congenital Hypothyroidism Related to Select Demographic Factors: Data From the United States, California, Massachusetts, New York, and Texas. PEDIATRICS. 125(Supplement_2). S37–S47. 151 indexed citations

10.

Case, Amy P., et al.. (2008). Proximity of pediatric genetic services to children with birth defects in Texas. Birth Defects Research Part A Clinical and Molecular Teratology. 82(11). 795–798. 11 indexed citations

11.

Drummond‐Borg, Margaret, et al.. (2003). Newborn screening for congenital hypothyroidism: the Texas experience.. PubMed. 99(9). 50–2. 1 indexed citations

12.

Drummond‐Borg, Margaret, et al.. (2002). Genetic susceptibility to aminoglycoside ototoxicity: How many are at risk?. Genetics in Medicine. 4(5). 336–345. 75 indexed citations

13.

Yang, Yaping, Margaret Drummond‐Borg, & Jaime Garcia‐Heras. (2001). Molecular analysis of phenylketonuria (PKU) in newborns from Texas. Human Mutation. 17(6). 523–523. 10 indexed citations

14.

Kukolich, Mary K., Anita S. Kulharya, S. M. Jalal, & Margaret Drummond‐Borg. (1989). Trisomy 22: No longer an enigma. American Journal of Medical Genetics. 34(4). 541–544. 25 indexed citations

15.

Drummond‐Borg, Margaret, S S Deeb, & Arno G. Motulsky. (1989). Molecular patterns of X chromosome-linked color vision genes among 134 men of European ancestry.. Proceedings of the National Academy of Sciences. 86(3). 983–987. 84 indexed citations

16.

Drummond‐Borg, Margaret, et al.. (1988). Nonfluorescent dicentric Y in males with hypospadias. The Journal of Pediatrics. 113(3). 469–473. 4 indexed citations

17.

Drummond‐Borg, Margaret, S S Deeb, & Arno G. Motulsky. (1988). Molecular basis of abnormal red-green color vision: a family with three types of color vision defects.. PubMed. 43(5). 675–83. 15 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