Hannah Wand

1.8k total citations
23 papers, 484 citations indexed

About

Hannah Wand is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Hannah Wand has authored 23 papers receiving a total of 484 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Rheumatology. Recurrent topics in Hannah Wand's work include BRCA gene mutations in cancer (10 papers), Genomics and Rare Diseases (7 papers) and Genetic Associations and Epidemiology (5 papers). Hannah Wand is often cited by papers focused on BRCA gene mutations in cancer (10 papers), Genomics and Rare Diseases (7 papers) and Genetic Associations and Epidemiology (5 papers). Hannah Wand collaborates with scholars based in United States, Australia and Canada. Hannah Wand's co-authors include Matt W. Wright, Carlos D. Bustamante, James Zou, Barbara A. Koenig, Kristy Crooks, Deborah Ritter, Stephanie M. Fullerton, Sharon E. Plon, Lucia A. Hindorff and Erin M. Ramos and has published in prestigious journals such as Circulation, Nature Genetics and PLoS ONE.

In The Last Decade

Hannah Wand

23 papers receiving 471 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hannah Wand United States	13	195	107	66	63	48	23	484
P. Engstrom United States	6	220 1.1×	139 1.3×	62 0.9×	64 1.0×	31 0.6×	9	714
Julie Richer Canada	13	399 2.0×	202 1.9×	46 0.7×	103 1.6×	35 0.7×	34	670
Milene Raiol de Moraes Brazil	5	172 0.9×	114 1.1×	38 0.6×	40 0.6×	30 0.6×	7	515
Terri H. Beaty United States	18	364 1.9×	184 1.7×	81 1.2×	55 0.9×	38 0.8×	53	783
Sandra Nestler-Parr United States	4	216 1.1×	109 1.0×	60 0.9×	46 0.7×	15 0.3×	6	562
Christine M. Cutillo United States	7	202 1.0×	118 1.1×	21 0.3×	60 1.0×	18 0.4×	7	504
T. Beck United States	9	139 0.7×	221 2.1×	87 1.3×	33 0.5×	38 0.8×	12	566
Nathalie de Lourdes Souza Dewulf Brazil	13	111 0.6×	516 4.8×	76 1.2×	53 0.8×	24 0.5×	33	833
James Ding United Kingdom	15	95 0.5×	295 2.8×	88 1.3×	34 0.5×	43 0.9×	26	601
Martha Matsumoto United States	13	128 0.7×	157 1.5×	57 0.9×	16 0.3×	67 1.4×	19	554

Countries citing papers authored by Hannah Wand

Since Specialization

Citations

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

Fields of papers citing papers by Hannah Wand

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hannah Wand

This figure shows the co-authorship network connecting the top 25 collaborators of Hannah Wand. A scholar is included among the top collaborators of Hannah Wand 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 Hannah Wand. Hannah Wand 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:

20 of 20 papers shown

Hull, Leland E., Aaron W. Aday, Quan M. Bui, et al.. (2025). Direct-to-Consumer Genetic Testing for Cardiovascular Disease: A Scientific Statement From the American Heart Association. Circulation. 151(14). e905–e917. 5 indexed citations

Christian, Susan, Amy J. L. Baker, Barbara B. Biesecker, et al.. (2024). Evaluation of face validity and core concepts of a novel knowledge scale for inherited heart disease: A pilot study. Journal of Genetic Counseling. 34(2). e1995–e1995. 2 indexed citations

Reddi, Honey V., Hannah Wand, Nancy C. Rose, et al.. (2023). The clinical application of polygenic risk scores: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 25(5). 100803–100803. 37 indexed citations

Wand, Hannah, Daphne Oluwaseun Martschenko, John S. Witte, et al.. (2023). Re-envisioning community genetics: community empowerment in preventive genomics. Journal of Community Genetics. 14(5). 459–469. 2 indexed citations

Reddi, Honey V., Hannah Wand, Birgit Funke, et al.. (2023). Laboratory perspectives in the development of polygenic risk scores for disease: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 25(5). 100804–100804. 13 indexed citations

Martschenko, Daphne Oluwaseun, Hannah Wand, Jennifer L. Young, & Genevieve L. Wojcik. (2023). Including multiracial individuals is crucial for race, ethnicity and ancestry frameworks in genetics and genomics. Nature Genetics. 55(6). 895–900. 18 indexed citations

Wand, Hannah, Sarah S. Kalia, Benjamin M. Helm, et al.. (2023). Clinical genetic counseling and translation considerations for polygenic scores in personalized risk assessments: A Practice Resource from the National Society of Genetic Counselors. Journal of Genetic Counseling. 32(3). 558–575. 18 indexed citations

O’Sullivan, Jack W., Anna Shcherbina, Johanne Marie Justesen, et al.. (2021). Combining Clinical and Polygenic Risk Improves Stroke Prediction Among Individuals With Atrial Fibrillation. Circulation Genomic and Precision Medicine. 14(3). e003168–e003168. 28 indexed citations

Hallquist, Miranda L. G., Kelly E. Ormond, Juliann M. Savatt, et al.. (2021). Application of a framework to guide genetic testing communication across clinical indications. Genome Medicine. 13(1). 71–71. 18 indexed citations

10.

Popejoy, Alice B., Kristy Crooks, Stephanie M. Fullerton, et al.. (2020). Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures. The American Journal of Human Genetics. 107(1). 72–82. 50 indexed citations

11.

Banda, Juan M., Ashish Sarraju, Fahim Abbasi, et al.. (2019). Finding missed cases of familial hypercholesterolemia in health systems using machine learning. npj Digital Medicine. 2(1). 23–23. 77 indexed citations

12.

Peay, Holly L., Ryan Fischer, Janice Tzeng, et al.. (2019). Gene therapy as a potential therapeutic option for Duchenne muscular dystrophy: A qualitative preference study of patients and parents. PLoS ONE. 14(5). e0213649–e0213649. 29 indexed citations

13.

Wand, Hannah, Amy C. Sturm, Lori H. Erby, Iris Kindt, & William M. P. Klein. (2019). Genetic testing preferences and intentions in patients with clinically diagnosed familial hypercholesterolemia. Journal of Genetic Counseling. 29(6). 919–927. 1 indexed citations

14.

Peay, Holly L., Ryan Fischer, Katherine Beaverson, et al.. (2018). Parent and Adult Patient Attitudes About Gene Therapy as a Therapeutic Option for Duchenne Muscular Dystrophy. Value in Health. 21. S256–S256. 5 indexed citations

15.

Popejoy, Alice B., Deborah Ritter, Kristy Crooks, et al.. (2018). The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics. Human Mutation. 39(11). 1713–1720. 95 indexed citations

16.

Haddon, D. James, Hannah Wand, Justin A. Jarrell, et al.. (2017). Proteomic Analysis of Sera from Individuals with Diffuse Cutaneous Systemic Sclerosis Reveals a Multianalyte Signature Associated with Clinical Improvement during Imatinib Mesylate Treatment. The Journal of Rheumatology. 44(5). 631–638. 17 indexed citations

17.

Lee, Jung‐Rok, D. James Haddon, Hannah Wand, et al.. (2016). Multiplex giant magnetoresistive biosensor microarrays identify interferon-associated autoantibodies in systemic lupus erythematosus. Scientific Reports. 6(1). 27623–27623. 29 indexed citations

18.

Haddon, D. James, Justin A. Jarrell, Hannah Wand, et al.. (2015). Mapping epitopes of U1-70K autoantibodies at single-amino acid resolution. Autoimmunity. 48(8). 513–523. 12 indexed citations

19.

Wand, Hannah, et al.. (2015). O12.3 Multicultural survey – 20 years on: trends in chinese and thai female sex worker demographics and sexual health in sydney. Sexually Transmitted Infections. 91(Suppl 2). A51.2–A51. 1 indexed citations

20.

Borges, Adair L., et al.. (2014). Differential Locus Expansion Distinguishes Toxoplasmatinae Species and Closely Related Strains of Toxoplasma gondii. mBio. 5(1). e01003–13. 16 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