Anne L. Matthews

880 total citations
31 papers, 639 citations indexed

About

Anne L. Matthews is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Anne L. Matthews has authored 31 papers receiving a total of 639 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 6 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Anne L. Matthews's work include BRCA gene mutations in cancer (7 papers), Hearing, Cochlea, Tinnitus, Genetics (4 papers) and Prenatal Screening and Diagnostics (4 papers). Anne L. Matthews is often cited by papers focused on BRCA gene mutations in cancer (7 papers), Hearing, Cochlea, Tinnitus, Genetics (4 papers) and Prenatal Screening and Diagnostics (4 papers). Anne L. Matthews collaborates with scholars based in United States, United Kingdom and France. Anne L. Matthews's co-authors include Nathaniel H. Robin, MaryAnn O’Riordan, Georgia L. Wiesner, Richard J. Smith, John Guillebaud, J. Bonnar, Gail S. Murray, Eric T. Juengst, Marni J. Falk and Mary Ann O’Riordan and has published in prestigious journals such as The Lancet, The FASEB Journal and The American Journal of Human Genetics.

In The Last Decade

Anne L. Matthews

30 papers receiving 603 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anne L. Matthews United States	13	292	178	147	86	84	31	639
Angelina Xavier Acosta Brazil	18	152 0.5×	75 0.4×	123 0.8×	30 0.3×	25 0.3×	79	850
Paul Lancaster Australia	13	70 0.2×	193 1.1×	463 3.1×	47 0.5×	16 0.2×	21	877
Anna Morgan Italy	18	125 0.4×	77 0.4×	19 0.1×	62 0.7×	248 3.0×	84	801
Sam Riedijk Netherlands	17	263 0.9×	68 0.4×	291 2.0×	57 0.7×	7 0.1×	37	889
Karen Fieggen South Africa	13	125 0.4×	50 0.3×	70 0.5×	26 0.3×	34 0.4×	42	390
G. Stanimir Canada	11	61 0.2×	60 0.3×	43 0.3×	20 0.2×	47 0.6×	20	618
Eric A. Evans United States	11	260 0.9×	47 0.3×	279 1.9×	19 0.2×	9 0.1×	21	743
Gabrielle J. Halpern Israel	13	243 0.8×	25 0.1×	80 0.5×	120 1.4×	18 0.2×	23	737
Shao‐Yin Chu Taiwan	13	119 0.4×	73 0.4×	54 0.4×	43 0.5×	6 0.1×	52	491
Loane Skene Australia	15	271 0.9×	245 1.4×	183 1.2×	71 0.8×	2 0.0×	82	840

Countries citing papers authored by Anne L. Matthews

Since Specialization

Citations

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

Fields of papers citing papers by Anne L. Matthews

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anne L. Matthews. 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 Anne L. Matthews. The network helps show where Anne L. Matthews may publish in the future.

Co-authorship network of co-authors of Anne L. Matthews

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

All Works

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20 of 20 papers shown

Hogan, Elizabeth, et al.. (2022). North American genetic counselors' approach to collecting and using ancestry in clinical practice. Journal of Genetic Counseling. 32(2). 462–474. 1 indexed citations

Goldenberg, Aaron J., et al.. (2022). Lived experiences of individuals with cystic fibrosis on CFTR-modulators. BMC Pulmonary Medicine. 22(1). 42–42. 11 indexed citations

Reid, Hamish, et al.. (2017). Infographic: physical activity for pregnant women. British Journal of Sports Medicine. 52(8). 532–533. 13 indexed citations

Darrah, Rebecca, et al.. (2016). Growth Deficiency in Cystic Fibrosis Is Observable at Birth and Predictive of Early Pulmonary Function. Biological Research For Nursing. 18(5). 498–504. 11 indexed citations

Wood, Michael D., et al.. (2015). Strategies for engaging with future radiation protection professionals: a public outreach case study. Journal of Radiological Protection. 35(4). N25–N32. 1 indexed citations

Acheson, Louise S., et al.. (2004). Clinical consult: Marfan syndrome. Primary Care Clinics in Office Practice. 31(3). 739–742. 13 indexed citations

Matthews, Anne L., et al.. (2004). Clinical consult: iron overload—hereditary hemochromatosis. Primary Care Clinics in Office Practice. 31(3). 767–770. 7 indexed citations

Wiesner, Georgia L., et al.. (2004). Clinical consult: developmental delay/fragile X syndrome. Primary Care Clinics in Office Practice. 31(3). 621–625. 5 indexed citations

Falk, Marni J., et al.. (2003). Medical geneticists' duty to warn at‐risk relatives for genetic disease. American Journal of Medical Genetics Part A. 120A(3). 374–380. 67 indexed citations

10.

Robin, Nathaniel H., Richard J. Smith, & Anne L. Matthews. (2003). Genetic Testing for Deafness in Clinical Practice. Audiological Medicine. 1(1). 89–93. 5 indexed citations

11.

Robin, Nathaniel H., Richard J. Smith, & Anne L. Matthews. (2003). Genetic Testing for Deafness in Clinical Practice. Audiological Medicine. 1(1). 89–93. 2 indexed citations

12.

Wiesner, Georgia L., et al.. (2002). Duty to warn at‐risk relatives for genetic disease: Genetic counselors' clinical experience. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 119C(1). 27–34. 94 indexed citations

13.

Matthews, Anne L., et al.. (2001). Genetic Testing and Genetic Counseling for Deafness: The Future Is Here. The Laryngoscope. 111(4). 715–718. 14 indexed citations

14.

Ormond, Kelly E., et al.. (2000). Recommendations for Telephone Counseling. Journal of Genetic Counseling. 9(1). 63–71. 32 indexed citations

15.

Murray, Gail S., et al.. (2000). Parental Attitudes toward Genetic Testing for Pediatric Deafness. The American Journal of Human Genetics. 67(6). 1621–1625. 109 indexed citations

16.

Matthews, Anne L.. (1999). Chromosomal Abnormalities: Trisomy 18, Trisomy 13, Deletions, and Microdeletions. The Journal of Perinatal & Neonatal Nursing. 13(2). 59–75. 11 indexed citations

17.

Matthews, Anne L.. (1990). Known fetal malformations during pregnancy: a human experience of loss.. PubMed. 26(3). 168–75. 14 indexed citations

18.

Matthews, Anne L., et al.. (1988). The mucolytic effect of Sputolosin in horses with respiratory disease. Veterinary Record. 122(5). 106–108. 3 indexed citations

19.

Matthews, Anne L., et al.. (1977). Word Processing: More a Matter of Skills Than Equipment..

20.

Guillebaud, John, et al.. (1976). MENSTRUAL BLOOD-LOSS WITH INTRAUTERINE DEVICES. The Lancet. 307(7956). 387–390. 78 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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