Sandra Daack‐Hirsch

6.0k total citations
71 papers, 2.9k citations indexed

About

Sandra Daack‐Hirsch is a scholar working on Genetics, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Sandra Daack‐Hirsch has authored 71 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Genetics, 22 papers in Molecular Biology and 14 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Sandra Daack‐Hirsch's work include Cleft Lip and Palate Research (30 papers), BRCA gene mutations in cancer (20 papers) and Craniofacial Disorders and Treatments (17 papers). Sandra Daack‐Hirsch is often cited by papers focused on Cleft Lip and Palate Research (30 papers), BRCA gene mutations in cancer (20 papers) and Craniofacial Disorders and Treatments (17 papers). Sandra Daack‐Hirsch collaborates with scholars based in United States, Brazil and Philippines. Sandra Daack‐Hirsch's co-authors include Jeffrey C. Murray, Paul A. Romitti, Mary L. Marazita, Ronald G. Munger, Andrew C. Lidral, Alexandre R. Vieira, Elena V. Semina, Trudy L. Burns, Lisa Shah and Martha Driessnack and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and PLoS ONE.

In The Last Decade

Sandra Daack‐Hirsch

68 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandra Daack‐Hirsch United States 26 2.2k 1.2k 324 295 244 71 2.9k
Iain McIntosh United States 34 2.4k 1.1× 1.7k 1.4× 238 0.7× 361 1.2× 230 0.9× 83 4.1k
Iêda M. Orioli Brazil 25 997 0.4× 430 0.4× 202 0.6× 591 2.0× 213 0.9× 64 2.0k
Helga V. Toriello United States 32 1.4k 0.6× 1.3k 1.1× 206 0.6× 430 1.5× 266 1.1× 97 3.1k
Howard M. Saal United States 33 2.4k 1.1× 1.3k 1.1× 285 0.9× 470 1.6× 395 1.6× 114 4.2k
Têmis Maria Félix Brazil 22 990 0.4× 638 0.5× 179 0.6× 229 0.8× 98 0.4× 97 1.7k
Kenneth N. Rosenbaum United States 26 1.0k 0.4× 627 0.5× 254 0.8× 344 1.2× 99 0.4× 59 2.2k
Agnes Bankier Australia 27 990 0.4× 767 0.6× 198 0.6× 389 1.3× 55 0.2× 80 2.0k
Rita Mingarelli Italy 28 1.1k 0.5× 1.4k 1.2× 105 0.3× 197 0.7× 91 0.4× 113 2.6k
Júlio César Voltarelli Brazil 28 483 0.2× 564 0.5× 499 1.5× 695 2.4× 230 0.9× 102 2.7k
Jaime L. Frías United States 34 1.4k 0.6× 816 0.7× 210 0.6× 879 3.0× 287 1.2× 119 3.3k

Countries citing papers authored by Sandra Daack‐Hirsch

Since Specialization
Citations

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

Fields of papers citing papers by Sandra Daack‐Hirsch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandra Daack‐Hirsch. 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 Sandra Daack‐Hirsch. The network helps show where Sandra Daack‐Hirsch may publish in the future.

Co-authorship network of co-authors of Sandra Daack‐Hirsch

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

All Works

20 of 20 papers shown
1.
Buck, Harleah G., et al.. (2025). The Prevalence of Malnutrition in Children With Congenital Heart Disease: A Meta-Analysis. Journal of Pediatric Health Care.
2.
Dickinson, Amanda, Huan Liu, Jennifer Standley, et al.. (2022). Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes. The American Journal of Human Genetics. 110(1). 71–91. 5 indexed citations
3.
Seven, Memnun, Lisa Shah, Sandra Daack‐Hirsch, & Hülya Yazıcı. (2020). Experiences of BRCA1/2 Gene Mutation–Positive Women With Cancer in Communicating Genetic Risk to Their Relatives. Cancer Nursing. 44(3). E142–E150. 16 indexed citations
4.
Daack‐Hirsch, Sandra, et al.. (2019). Bringing Personalized Medicine to a PACT Program: A Quality Improvement Project. Journal of the American Psychiatric Nurses Association. 26(1). 77–85. 2 indexed citations
5.
Laurino, Mercy, et al.. (2017). Parent-Child Communication about Congenital Adrenal Hyperplasia: Filipino Mothers’ Experience. Acta Medica Philippina. 51(3).
6.
Conley, Yvette P., Margaret Heitkemper, Donna O. McCarthy, et al.. (2015). Educating future nursing scientists: Recommendations for integrating omics content in PhD programs. Nursing Outlook. 63(4). 417–427. 26 indexed citations
7.
Daack‐Hirsch, Sandra, et al.. (2013). ‘Information is information’: a public perspective on incidental findings in clinical and research genome‐based testing. Clinical Genetics. 84(1). 11–18. 65 indexed citations
8.
Daack‐Hirsch, Sandra, et al.. (2013). Integrating Genetics and Genomics into Nursing Curricula. Nursing Clinics of North America. 48(4). 661–669. 20 indexed citations
9.
Daack‐Hirsch, Sandra, et al.. (2013). Parental perspectives on the diagnostic process for Duchenne and Becker muscular dystrophy. American Journal of Medical Genetics Part A. 161(4). 687–695. 9 indexed citations
10.
Driessnack, Martha, Sandra Daack‐Hirsch, Nancy R. Downing, et al.. (2013). The disclosure of incidental genomic findings: an “ethically important moment” in pediatric research and practice. Journal of Community Genetics. 4(4). 435–444. 21 indexed citations
11.
Williams, Janet K., Sandra Daack‐Hirsch, Martha Driessnack, et al.. (2012). Researcher and Institutional Review Board Chair Perspectives on Incidental Findings in Genomic Research. Genetic Testing and Molecular Biomarkers. 16(6). 508–513. 26 indexed citations
12.
Letra, Ariadne, Walid D. Fakhouri, Renato Menezes, et al.. (2012). Interaction between IRF6 and TGFA Genes Contribute to the Risk of Nonsyndromic Cleft Lip/Palate. PLoS ONE. 7(9). e45441–e45441. 43 indexed citations
13.
Daack‐Hirsch, Sandra, et al.. (2012). A Practical First Step to Integrating Genetics Into the Curriculum. Journal of Nursing Education. 51(5). 294–298. 18 indexed citations
14.
Jugessur, Astanand, Min Shi, Håkon K. Gjessing, et al.. (2010). Maternal Genes and Facial Clefts in Offspring: A Comprehensive Search for Genetic Associations in Two Population-Based Cleft Studies from Scandinavia. PLoS ONE. 5(7). e11493–e11493. 34 indexed citations
15.
Jugessur, Astanand, Min Shi, Håkon K. Gjessing, et al.. (2010). Fetal genetic risk of isolated cleft lip only versus isolated cleft lip and palate: A subphenotype analysis using two population-based studies of orofacial clefts in scandinavia. Birth Defects Research Part A Clinical and Molecular Teratology. 91(2). 85–92. 25 indexed citations
16.
Scott, Nicole, Seth M. Weinberg, Katherine Neiswanger, et al.. (2005). Dermatoglyphic Fingerprint Heterogeneity Among Individuals with Nonsyndromic Cleft Lip With or Without Cleft Palate and Their Unaffected Relatives in China and the Philippines. Human Biology. 77(2). 257–266. 13 indexed citations
17.
Munger, Ronald G., et al.. (2004). Maternal vitamin B‐6 and folate status and risk of oral cleft birth defects in the Philippines. Birth Defects Research Part A Clinical and Molecular Teratology. 70(7). 464–471. 65 indexed citations
18.
Cooper, Margaret E., Sandra Daack‐Hirsch, Min Shi, et al.. (2003). Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families. American Journal of Medical Genetics Part A. 125A(1). 17–22. 58 indexed citations
19.
Schutte, Brian C., Ann M. Basart, Yoriko Watanabe, et al.. (1999). Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome. American Journal of Medical Genetics. 84(2). 145–150. 54 indexed citations
20.
Semina, Elena V., Robert E. Ferrell, Helen A. Mintz-Hittner, et al.. (1998). A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD. Nature Genetics. 19(2). 167–170. 299 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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