Theresa A. Grebe

4.0k total citations
34 papers, 879 citations indexed

About

Theresa A. Grebe is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Theresa A. Grebe has authored 34 papers receiving a total of 879 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 18 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Theresa A. Grebe's work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (5 papers) and Prenatal Screening and Diagnostics (5 papers). Theresa A. Grebe is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (5 papers) and Prenatal Screening and Diagnostics (5 papers). Theresa A. Grebe collaborates with scholars based in United States, Germany and Canada. Theresa A. Grebe's co-authors include Carol L. Clericuzio, David Chitayat, Stephen W. Scherer, Ariane Mandel, Barbara R. Pober, Sarah Cox, Martin Li, Teresa Costa, L.-C. Tsui and Joann Bodurtha and has published in prestigious journals such as Nature Genetics, PLoS ONE and PEDIATRICS.

In The Last Decade

Theresa A. Grebe

32 papers receiving 851 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Theresa A. Grebe United States 16 458 449 102 92 87 34 879
Alexandra Afenjar France 16 621 1.4× 521 1.2× 69 0.7× 113 1.2× 36 0.4× 42 1.0k
Patricia I. Bader United States 18 584 1.3× 619 1.4× 92 0.9× 180 2.0× 89 1.0× 32 1.1k
Paul C. Lott United States 13 299 0.7× 1.3k 2.9× 67 0.7× 139 1.5× 111 1.3× 23 1.7k
Abdul Noor Canada 20 620 1.4× 823 1.8× 145 1.4× 118 1.3× 35 0.4× 42 1.4k
Bhooma Thiruvahindrapuram Canada 14 500 1.1× 420 0.9× 147 1.4× 123 1.3× 42 0.5× 47 880
Nathalie Van der Aa Belgium 19 388 0.8× 412 0.9× 92 0.9× 38 0.4× 47 0.5× 26 809
A. Moncla France 17 748 1.6× 633 1.4× 121 1.2× 174 1.9× 70 0.8× 29 1.1k
Gladys Ho Australia 19 855 1.9× 778 1.7× 219 2.1× 67 0.7× 29 0.3× 43 1.4k
Marzia Pollazzon Italy 14 494 1.1× 368 0.8× 143 1.4× 43 0.5× 42 0.5× 31 692
Séverine Drunat France 21 443 1.0× 581 1.3× 65 0.6× 144 1.6× 53 0.6× 57 1.1k

Countries citing papers authored by Theresa A. Grebe

Since Specialization
Citations

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

Fields of papers citing papers by Theresa A. Grebe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Theresa A. Grebe. 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 Theresa A. Grebe. The network helps show where Theresa A. Grebe may publish in the future.

Co-authorship network of co-authors of Theresa A. Grebe

This figure shows the co-authorship network connecting the top 25 collaborators of Theresa A. Grebe. A scholar is included among the top collaborators of Theresa A. Grebe 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 Theresa A. Grebe. Theresa A. Grebe 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.
Grebe, Theresa A., et al.. (2025). Systemic JAK inhibitors for treatment of cutaneous manifestations in a patient with SPINK5 variants: A case report and review of the literature. Pediatric Allergy and Immunology. 36(2). e70039–e70039. 1 indexed citations
2.
3.
Grebe, Theresa A., George Khushf, John M. Greally, et al.. (2024). Clinical utility of polygenic risk scores for embryo selection: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 26(4). 101052–101052. 8 indexed citations
4.
5.
Gonçalves, Luís F., et al.. (2021). Prenatal diagnosis of bilateral retinoblastomas by multimodality fetal imaging: case report and review of the literature. Clinical Imaging. 78. 121–126. 6 indexed citations
6.
7.
Narayanan, Vinodh, et al.. (2016). An atypical presentation of ACAD9 deficiency: Diagnosis by whole exome sequencing broadens the phenotypic spectrum and alters treatment approach. Molecular Genetics and Metabolism Reports. 10. 38–44. 11 indexed citations
8.
Appavu, Brian, et al.. (2016). Electroclinical phenotypes and outcomes in TBC1D24-related epilepsy. Epileptic Disorders. 18(3). 324–328. 13 indexed citations
9.
Grebe, Theresa A., et al.. (2015). Chronic pain in Noonan Syndrome: A previously unreported but common symptom. American Journal of Medical Genetics Part A. 167(12). 2998–3005. 13 indexed citations
10.
Alter, Mark D., Keri E. Ramsey, David W. Craig, et al.. (2011). Autism and Increased Paternal Age Related Changes in Global Levels of Gene Expression Regulation. PLoS ONE. 6(2). e16715–e16715. 76 indexed citations
11.
Brautbar, Ariel, Jing Wang, José E. Abdenur, et al.. (2008). The mitochondrial 13513G>A mutation is associated with Leigh disease phenotypes independent of complex I deficiency in muscle. Molecular Genetics and Metabolism. 94(4). 485–490. 35 indexed citations
12.
Nakabayashi, Kazuhiko, Bridget A. Fernandez, Ikuko Teshima, et al.. (2002). Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome. Genomics. 79(2). 186–196. 25 indexed citations
13.
14.
Conroy, Jeffrey M., Theresa A. Grebe, Karen D. Tsuchiya, et al.. (1997). Balanced Translocation 46, XY, t(2;15)(q37.2;q11.2) Associated with Atypical Prader-Willi Syndrome. The American Journal of Human Genetics. 61(2). 388–394. 43 indexed citations
15.
Grebe, Theresa A. & Carol L. Clericuzio. (1996). Autosomal dominant inheritance of hypothalamic hamartoma associated with polysyndactyly: Heterogeneity or variable expressivity?. American Journal of Medical Genetics. 66(2). 129–137. 18 indexed citations
16.
Biesecker, Leslie G., S Kang, A. A. Schaffer, et al.. (1996). Exclusion of candidate loci and cholesterol biosynthetic abnormalities in familial Pallister-Hall syndrome.. Journal of Medical Genetics. 33(11). 947–951. 7 indexed citations
17.
Mercier, Bernard, Xavier Estivill, Núria Morral, et al.. (1994). Complete detection of mutations in cystic fibrosis patients of Native American origin. Human Genetics. 94(6). 629–32. 24 indexed citations
18.
Grebe, Theresa A., et al.. (1993). Further delineation of the epidermal nevus syndrome: Two cases with new findings and literature review. American Journal of Medical Genetics. 47(1). 24–30. 50 indexed citations
19.
Grebe, Theresa A., et al.. (1992). 7p Deletion syndrome: An adult with mild manifestations. American Journal of Medical Genetics. 44(1). 18–23. 4 indexed citations
20.
Schallreuter, K. U., Theresa A. Grebe, Mark R. Pittelkow, & John M. Wood. (1991). [<sup>3</sup>H]-13-<i>cis</i>-Retinoic Acid Covalently Binds to Thioredoxin Reductase in Human Keratinocytes. Skin Pharmacology and Physiology. 4(1). 14–20. 11 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

Breakdown of academic impact, for papers by Alexandra Afenjar Breakdown of academic impact, for papers by Patricia I. Bader Breakdown of academic impact, for papers by Paul C. Lott Breakdown of academic impact, for papers by Abdul Noor Breakdown of academic impact, for papers by Bhooma Thiruvahindrapuram Breakdown of academic impact, for papers by Nathalie Van der Aa Breakdown of academic impact, for papers by A. Moncla Breakdown of academic impact, for papers by Gladys Ho Breakdown of academic impact, for papers by Marzia Pollazzon Breakdown of academic impact, for papers by Séverine Drunat
Rankless by CCL
2026