Katie Bergstrom

1.4k total citations
21 papers, 245 citations indexed

About

Katie Bergstrom is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Katie Bergstrom has authored 21 papers receiving a total of 245 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Katie Bergstrom's work include Genomics and Rare Diseases (4 papers), BRCA gene mutations in cancer (3 papers) and Childhood Cancer Survivors' Quality of Life (3 papers). Katie Bergstrom is often cited by papers focused on Genomics and Rare Diseases (4 papers), BRCA gene mutations in cancer (3 papers) and Childhood Cancer Survivors' Quality of Life (3 papers). Katie Bergstrom collaborates with scholars based in United States, United Kingdom and Netherlands. Katie Bergstrom's co-authors include Sarah Scollon, Sharon E. Plon, D. Williams Parsons, Amy L. McGuire, Susan G. Hilsenbeck, Richard L. Street, Alison A. Bertuch, Laurence B. McCullough, Jill O. Robinson and Christine M. Eng and has published in prestigious journals such as Journal of Clinical Oncology, Blood and Cancer Research.

In The Last Decade

Katie Bergstrom

21 papers receiving 242 citations

Peers

Countries citing papers authored by Katie Bergstrom

Since Specialization

Citations

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

Fields of papers citing papers by Katie Bergstrom

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katie Bergstrom

This figure shows the co-authorship network connecting the top 25 collaborators of Katie Bergstrom. A scholar is included among the top collaborators of Katie Bergstrom 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 Katie Bergstrom. Katie Bergstrom 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

#	Title	Journal	Authors	Indexed citations
1	The genetics of vascular birthmarks	Clinics in Dermatology	Priya Mahajan, Katie Bergstrom et al.	8
2	Germline genetic mutations in pediatric cerebrovascular anomalies: a multidisciplinary approach to screening, testing, and management	Journal of Neurosurgery Pediatrics	Melissa A. LoPresti, Rebecca Du et al.	3
3	Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an “HHT‐like” syndrome in children	Molecular Genetics & Genomic Medicine	Joshua Hodgson, Lı́dia Ruiz et al.	28
4	Expansion of germline RPS20 mutation phenotype to include Diamond–Blackfan anemia	Human Mutation	Fujun Zhou, Lucas C. Reineke et al.	14
5	First case of neutropenia and thrombocytopenia in the setting of cerebral cavernous malformation 3	International Journal of Hematology	Clay T. Cohen, Katie Bergstrom et al.	2
6	Undergraduate Student Perceptions and Awareness of Genetic Counseling	Journal of Genetic Counseling	Amanda Gerard, Sarah Noblin et al.	12
7	Agents of empathy: How medical interpreters bridge sociocultural gaps in genomic sequencing disclosures with Spanish-speaking families	Patient Education and Counseling	Amanda M. Gutierrez, Jill O. Robinson et al.	16
8	Exome sequencing disclosures in pediatric cancer care: Patterns of communication among oncologists, genetic counselors, and parents	Patient Education and Counseling	Sarah Scollon, Mary A. Majumder et al.	16
9	PSTPIP1‐associated myeloid‐related proteinemia inflammatory syndrome: A rare cause of childhood neutropenia associated with systemic inflammation and hyperzincemia	Pediatric Blood & Cancer	Saman K. Hashmi, Katie Bergstrom et al.	20
10	Portero Versus Portador: Spanish Interpretation of Genomic Terminology During Whole Exome Sequencing Results Disclosure	Personalized Medicine	Amanda M. Gutierrez, Jill O. Robinson et al.	17
11	Integrated tumor and germline whole-exome sequencing identifies mutations in MAPK and PI3K pathway genes in an adolescent with rosette-forming glioneuronal tumor of the fourth ventricle	Molecular Case Studies	Frank Y. Lin, Katie Bergstrom et al.	17
12	Thrombopoietin Measurement as a Key Component in the Evaluation of Pediatric Thrombocytosis	Pediatric Blood & Cancer	Andrea N. Marcogliese, Katie Bergstrom et al.	6
13	Pediatric Cancer Genetics Research and an Evolving Preventive Ethics Approach for Return of Results after Death of the Subject	The Journal of Law Medicine & Ethics	Sarah Scollon, Katie Bergstrom et al.	4
14	Haemophilia B acquired from liver transplantation: a case report and literature review	Haemophilia	Katie Bergstrom, Alexandra M. Stevens et al.	6
15	Adenosine Deaminase 2 Deficiency As a Cause of Pure Red Cell Aplasia Mimicking Diamond Blackfan Anemia	Blood	Ghadir Sasa, M. Tarek Elghetany et al.	10
16	What’s in an exome? Diversity of diagnostic and incidental findings revealed by clinical tumor and germline sequencing of 100 children with solid tumors.	Journal of Clinical Oncology	D. Williams Parsons, Angshumoy Roy et al.	1
17	Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients	Genome Medicine	Sarah Scollon, Katie Bergstrom et al.	55
18	Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients	Genome Medicine	Sarah Scollon, Katie Bergstrom et al.	2
19	Abstract 11: Evaluating cancer susceptibility mutations and incidental findings from whole exome sequencing of sequentially diagnosed pediatric solid and brain tumor patients: Early results of the BASIC3 study	Cancer Research	Sharon E. Plon, Sarah Scollon et al.	1
20	[Liver transplantations at the Huddinge Hospital--experience, indications, needs].	PubMed	Groth Cg, G Lundgren et al.	1

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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