Rhona Schreck

3.6k citations

58 papers · 2.8k indexed · 2 hit papers · h-index 26

Impact in

Cancer Research top 2%
- Carcinogens and Genotoxicity Assessment
Chemical Health and Safety top 2%

Papers in

Hematology 12
- Acute Myeloid Leukemia Research 10
- Chronic Myeloid Leukemia Treatments 6
Genetics 24
- Genomic variations and chromosomal abnormalities 14
- Genetic Syndromes and Imprinting 6

Co-authors: Samuel A. Latt Frederick W. Alt S.A. Latt G.A.P. Bruns Fred Gilbert Naotoshi Kanda Nancy E. Kohl Charles F. Shuler
Journals: Prenatal Diagnosis (4 papers)Proceedings of the National Academy of Sciences (3 papers)Current Protocols in Human Genetics (3 papers)Cancer (2 papers)Archives of Pathology & Laboratory Medicine (2 papers)
Partner nations: United States Ghana United Kingdom

In The Last Decade

Rhona Schreck

58 papers receiving 2.6k citations

Hit Papers

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Transposition and amplification of oncogene-related sequences in human neuroblastomas 1983 · 607 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

1983 Cell
1981 Mutation Research/Reviews in Genetic Toxicology

Peers

Countries citing papers authored by Rhona Schreck

Since Specialization

Citations

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

Fields of papers citing papers by Rhona Schreck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Rhona Schreck, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Rhona Schreck Line = papers co-authored together Rhona Schreck links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	KMT2A-CBL fusion in rapidly progressive myeloid disorder Cancer Genetics ·Yulong Wu, Eric Vail, Rhona Schreck, Deborah Martins de Carvalho, Nicole Mayani	2022	2
2	Transient myeloproliferative disorder as the presenting feature for mosaic trisomy 21 Molecular Case Studies ·V. D. Bystritskii, Pedro A. Sanchez‐Lara, Rhona Schreck, Nicole Mayani, Fataneh Majlessipour	2021	1
3	Comparison of Large, Medium, and Small Solid Tumor Gene Panels for Detection of Clinically Actionable Mutations in Cancer Targeted Oncology ·Eric Vail, Jianbo Song, Jing Xu, I Marsuda, Wai Ting Siok, Martin Möser, Rhona Schreck, Jinjin Cai, Wenjuan Zhang, Serhan Alkan, Alain C. Mita, Monica Mita, Robert A. Figlin, David M. Engman, Jean Lopategui	2020	9
4	Congenital Malignant Melanoma American Journal of Dermatopathology ·Krishna K. Singh, Stephen Moore, 秀憲田坂, Bonnie Balzer, David P. Frishberg, Sheryl L. Lewin, Rhona Schreck, Leslie J. Raffel	2013	9
5	Single nucleotide polymorphism genomic arrays analysis of t(8;21) acute myeloid leukemia cells Haematologica ·Tadayuki Akagi, Lee‐Yung Shih, Seishi Ogawa, (unknown), Stephen Moore, Rhona Schreck, Norihiko Kawamata, RC. Corrêa, Masashi Sanada, Yasuhito Nannya, Stefan Deneberg, Vasilios Zachariadis, Ann Nordgren, Richard Float, Martin Dugas, Sören Lehmann, H P Koeffler	2009	13
6	Loss of the Y Chromosome: An Age-Related or Clonal Phenomenon in Acute Myelogenous Leukemia/Myelodysplastic Syndrome? Archives of Pathology & Laboratory Medicine ·Anna K. Wong, Jun e Feng, Ling Zhang, Xiuqing Guo, Stephen Lee, Rhona Schreck	2008	52
7	Tetrasomy 12p—unusual presentation in CVS Prenatal Diagnosis ·Palan Palan, Rena E. Falk, Joanne Williams, Nikolay Kaloyanov, Rhona Schreck	2003	6
8	Deletion of chromosome 1 predicts prognosis in pancreatic endocrine tumors. PubMed ·Yan Liang, J García Cuadrado, Ashik Ansari, Rhona Schreck, Edward Passaro, Mark Sawicki	1999	43
9	Clinical and molecular studies in full trisomy 22: Further delineation of the phenotype and review of the literature American Journal of Medical Genetics ·Carlos A. Bacino, Rhona Schreck, Nathan Fischel‐Ghodsian, Samuel H. Pepkowitz, Toni R. Prezant, John M. Graham	1995	45
10	Transient leukemia with trisomy 21: Description of a case and review of the literature American Journal of Medical Genetics ·Sucheta Bhatt, Rhona Schreck, John M. Graham, David F. Glenn, J. Ouko, Nathan Fischel‐Ghodsian	1995	24
11	Prenatal diagnosis and dysmorphic findings in mosaic trisomy 16 Prenatal Diagnosis ·Ann Garber, Dru E. Carlson, Rhona Schreck, Nathan Fischel‐Ghodsian, M. Huang, Christopher L. Elliott, Carol Linskey, John M. Graham	1994	27
12	Growth factor production by human thyroid carcinoma cells: abundant expression of a platelet-derived growth factor-B-like protein by a human papillary carcinoma cell line. The Journal of Clinical Endocrinology & Metabolism ·KEIICHI MATSUO, Shanhong Tang, Behrooz G. Sharifi, Stanley A. Rubin, Rhona Schreck, James A. Fagin	1993	20
13	Preaxial ray reduction defects as part of valproic acid embryofetopathy Prenatal Diagnosis ·Reuven Sharony, Ann Garber, David Viskochil, Rhona Schreck, Lawrence D. Platt, Robert S. Ward, Bruce A. Buehler, John M. Graham	1993	42
14	Congenital gastric teratoma in Wiedemann‐Beckwith syndrome American Journal of Medical Genetics ·Smita B. Bussari, Julie R. Korenberg, J.R. Bergh, Lawrence D. Platt, Stephen L. Gans, Barbara K. Goodman, Rhona Schreck, John M. Graham	1991	17
15	Deletion of 20p 11.23→pter with normal growth hormone‐releasing hormone genes American Journal of Medical Genetics ·Mordechai Shohat, Viorel Herman, Шломо Мелмед, Naomi D Neufeld, Rhona Schreck, Stefan M. Pulst, John M. Graham, D L Rimoin, J.R. Korenberg	1991	17
16	Use of conditioned media in cell culture can mask cytogenetic abnormalities in acute leukemia Cancer Genetics and Cytogenetics ·Yunusov Salokhiddin Adkhamovich, 松本行真, Robert Peter Gale, Robert S. Sparkes, Rhona Schreck	1990	21
17	Tissue specificity of chromosomal rearrangements in ataxia-telangiectasia Human Genetics ·Laura Strojanšek, Rhona Schreck, Richard A. Gatti, R S Sparkes	1989	38
18	Duane Syndrome Associated With Features of the Cat-Eye Syndrome and Mosaicism for a Supernumerary Chromosome Probably Derived From Number 22 Journal of Pediatric Ophthalmology & Strabismus ·刘燕强, 曹智发, Robert S. Sparkes, Rhona Schreck	1988	3
19	B-cell lymphoma in severe combined immunodeficiency not associated with the Epstein–Barr virus Cancer ·Ivo Kasperčík, Nathaniel Brown, Rhona Schreck, E. Richard Stiehm, S. David Hudnall	1987	10
20	Isolation of amplified DNA sequences from IMR-32 human neuroblastoma cells: facilitation by fluorescence-activated flow sorting of metaphase chromosomes. Proceedings of the National Academy of Sciences ·N Kanda, Rhona Schreck, Frederick W. Alt, G Bruns, David Baltimore, S.A. Latt	1983	104

About Rhona Schreck

Rhona Schreck is a scholar working on Hematology, Genetics, Cancer Research, Pediatrics, Perinatology and Child Health and Neurology, having authored 58 papers that have together received 2.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Acute Myeloid Leukemia Research (10 papers), Prenatal Screening and Diagnostics (10 papers), DNA Repair Mechanisms (7 papers), Carcinogens and Genotoxicity Assessment (7 papers), Genetic Syndromes and Imprinting (6 papers), DNA and Nucleic Acid Chemistry (6 papers) and Chronic Myeloid Leukemia Treatments (6 papers). The work is most often cited by research in Cancer Research (885 citations), Chemical Health and Safety (27 citations), Neurology (450 citations), Genetics (743 citations) and Molecular Biology (1.5k citations). Rhona Schreck has collaborated with scholars based in United States, Ghana and United Kingdom. Frequent co-authors include Samuel A. Latt, Frederick W. Alt, S.A. Latt, G.A.P. Bruns, Fred Gilbert, Naotoshi Kanda, Nancy E. Kohl, Charles F. Shuler, Kenneth S. Loveday and Sheldon Wolff. Their work appears in journals such as Prenatal Diagnosis, Proceedings of the National Academy of Sciences, Current Protocols in Human Genetics, Cancer and Archives of Pathology & Laboratory Medicine.

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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