Louise Amlie‐Wolf

408 total citations
6 papers, 54 citations indexed

About

Louise Amlie‐Wolf is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Louise Amlie‐Wolf has authored 6 papers receiving a total of 54 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Louise Amlie‐Wolf's work include BRCA gene mutations in cancer (2 papers), Ocular Disorders and Treatments (2 papers) and Congenital Ear and Nasal Anomalies (2 papers). Louise Amlie‐Wolf is often cited by papers focused on BRCA gene mutations in cancer (2 papers), Ocular Disorders and Treatments (2 papers) and Congenital Ear and Nasal Anomalies (2 papers). Louise Amlie‐Wolf collaborates with scholars based in United States, Nigeria and United Arab Emirates. Louise Amlie‐Wolf's co-authors include Joshua J. Zaritsky, Caroline Gluck, Laura Baker, Adele Schneider, Karen W. Gripp, Morgan Thomas, Tanya Bardakjian, Linda M. Reis, Elena V. Semina and Farzana Perwad and has published in prestigious journals such as Pediatric Nephrology, American Journal of Medical Genetics Part A and Delaware Journal of Public Health.

In The Last Decade

Louise Amlie‐Wolf

6 papers receiving 54 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Louise Amlie‐Wolf United States	4	26	21	18	17	14	6	54
Adele Mitrotti Italy	4	37 1.4×	40 1.9×	10 0.6×	43 2.5×	5 0.4×	6	71
Adrian Lungu Romania	5	6 0.2×	11 0.5×	6 0.3×	23 1.4×	9 0.6×	10	46
Rozemarijn Snoek Netherlands	6	47 1.8×	56 2.7×	39 2.2×	55 3.2×	9 0.6×	8	112
Priya Krithivasan India	2	27 1.0×	29 1.4×	7 0.4×	34 2.0×	2 0.1×	2	50
Nikta Forghani United States	3	15 0.6×	15 0.7×	9 0.5×	3 0.2×	4 0.3×	3	60
Lamisse Mansour‐Hendili France	5	21 0.8×	36 1.7×	10 0.6×	2 0.1×	15 1.1×	9	64
Kathleen Wallace United States	4	50 1.9×	17 0.8×	16 0.9×	2 0.1×	4 0.3×	7	75
Caroline M. Kolvenbach United States	3	5 0.2×	35 1.7×	20 1.1×	10 0.6×	9 0.6×	7	51
Mohamed Adil United States	4	5 0.2×	13 0.6×	5 0.3×	9 0.5×	7 0.5×	4	43
Andrea Titieni Germany	4	81 3.1×	81 3.9×	61 3.4×	12 0.7×	29 2.1×	5	125

Countries citing papers authored by Louise Amlie‐Wolf

Since Specialization

Citations

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

Fields of papers citing papers by Louise Amlie‐Wolf

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Louise Amlie‐Wolf. 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 Louise Amlie‐Wolf. The network helps show where Louise Amlie‐Wolf may publish in the future.

Co-authorship network of co-authors of Louise Amlie‐Wolf

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

All Works

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6 of 6 papers shown

1.

Sethna, Christine B., Onur Çil, Farzana Perwad, et al.. (2023). Genetic testing in children with nephrolithiasis and nephrocalcinosis. Pediatric Nephrology. 38(8). 2615–2622. 14 indexed citations

2.

Capasso, Jenina, et al.. (2023). SOX2 pathogenic variants with normal eyes: Expanding the phenotypic spectrum. American Journal of Medical Genetics Part A. 191(8). 2198–2203. 1 indexed citations

3.

Thomas, Morgan, Louise Amlie‐Wolf, Laura Baker, & Karen W. Gripp. (2021). The Genetic Testing Stewardship Program:. Delaware Journal of Public Health. 7(5). 20–23. 3 indexed citations

4.

Amlie‐Wolf, Louise, et al.. (2021). Review of 37 patients with SOX2 pathogenic variants collected by the Anophthalmia/Microphthalmia Clinical Registry and DNA research study. American Journal of Medical Genetics Part A. 188(1). 187–198. 10 indexed citations

5.

Amlie‐Wolf, Louise, Laura Baker, Morgan Thomas, et al.. (2021). Novel genetic testing model: A collaboration between genetic counselors and nephrology. American Journal of Medical Genetics Part A. 185(4). 1142–1150. 20 indexed citations

6.

Amlie‐Wolf, Louise, et al.. (2020). Three new patients with Steel syndrome and a Puerto Rican specific COL27A1 mutation. American Journal of Medical Genetics Part A. 182(4). 798–803. 6 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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