Barbara K. Goodman

2.2k total citations
48 papers, 1.5k citations indexed

About

Barbara K. Goodman is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Barbara K. Goodman has authored 48 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 14 papers in Genetics and 13 papers in Genetics. Recurrent topics in Barbara K. Goodman's work include Chronic Lymphocytic Leukemia Research (12 papers), Genomic variations and chromosomal abnormalities (11 papers) and Lymphoma Diagnosis and Treatment (8 papers). Barbara K. Goodman is often cited by papers focused on Chronic Lymphocytic Leukemia Research (12 papers), Genomic variations and chromosomal abnormalities (11 papers) and Lymphoma Diagnosis and Treatment (8 papers). Barbara K. Goodman collaborates with scholars based in United States, Canada and Taiwan. Barbara K. Goodman's co-authors include Michael T. Geraghty, Carlos A Tirado, Jon P. Gockerman, Joseph O. Moore, J. Brice Weinberg, George H. Thomas, Alicia D. Volkheimer, Julie Rutberg, Ryohei Furumai and Gilles Thomas and has published in prestigious journals such as Nature Genetics, The EMBO Journal and Blood.

In The Last Decade

Barbara K. Goodman

46 papers receiving 1.5k citations

Peers

Barbara K. Goodman

GENET

PFM

Gail Chuck United States

Takashi Sonoki Japan

Mohammed A. Aldahmesh Saudi Arabia

Josema Torres Spain

Hanan E. Shamseldin Saudi Arabia

S.A. Whitmore Australia

Leonarda Ianzano Italy

Carola G.M. van Berkel Netherlands

Saya Ito Japan

Hiromitsu Matsuzaki Japan

Gail Chuck United States

Barbara K. Goodman

1.3k ×1.7

290 ×0.8

GENET

113 ×0.4

GENET

118 ×0.5

PFM

291 ×1.5

Citations per year, relative to Barbara K. Goodman Barbara K. Goodman (= 1×) peers Gail Chuck

Countries citing papers authored by Barbara K. Goodman

Since Specialization

Citations

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

Fields of papers citing papers by Barbara K. Goodman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Barbara K. Goodman. 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 Barbara K. Goodman. The network helps show where Barbara K. Goodman may publish in the future.

Co-authorship network of co-authors of Barbara K. Goodman

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara K. Goodman. A scholar is included among the top collaborators of Barbara K. Goodman 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 Barbara K. Goodman. Barbara K. Goodman 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

Goodman, Barbara K., et al.. (2024). Philanthropy’s Role in Catalyzing New Uses for Approved Treatments. 1(1).

Goodman, Barbara K., et al.. (2023). Philanthropy’s Role in Catalyzing New Uses for Approved Treatments.

Brothman, Arthur R., Michelle Dolan, Barbara K. Goodman, et al.. (2011). College of American Pathologists/American College of Medical Genetics proficiency testing for constitutional cytogenomic microarray analysis. Genetics in Medicine. 13(9). 765–769. 12 indexed citations

Perkinson, Kathryn, et al.. (2010). A Single Tube, Four-Color Flow Cytometry Assay for Evaluation of ZAP-70 and CD38 Expression in Chronic Lymphocytic Leukemia. American Journal of Clinical Pathology. 133(5). 708–717. 8 indexed citations

Friedman, Daphne R., J. Brice Weinberg, William T. Barry, et al.. (2009). A Genomic Approach to Improve Prognosis and Predict Therapeutic Response in Chronic Lymphocytic Leukemia. Clinical Cancer Research. 15(22). 6947–6955. 28 indexed citations

Jardim, Melanie, Qinhong Wang, Ryohei Furumai, et al.. (2009). Reduced ATR or Chk1 Expression Leads to Chromosome Instability and Chemosensitization of Mismatch Repair–deficient Colorectal Cancer Cells. Molecular Biology of the Cell. 20(17). 3801–3809. 26 indexed citations

Lanasa, Mark C., Sallie D. Allgood, Alicia D. Volkheimer, et al.. (2009). Single-cell analysis reveals oligoclonality among ‘low-count’ monoclonal B-cell lymphocytosis. Leukemia. 24(1). 133–140. 49 indexed citations

Gong, Jerald Z., Barbara K. Goodman, Patrick J. Buckley, et al.. (2007). Clinicopathologic Findings in High-Grade B-Cell Lymphomas With Typical Burkitt Morphologic Features but Lacking theMYCTranslocation. American Journal of Clinical Pathology. 128(6). 981–991. 22 indexed citations

Volkheimer, Alicia D., J. Brice Weinberg, John F. Whitesides, et al.. (2006). Progressive immunoglobulin gene mutations in chronic lymphocytic leukemia: evidence for antigen-driven intraclonal diversification. Blood. 109(4). 1559–1567. 28 indexed citations

10.

Quigley, Denise I., Marie McDonald, Priya S. Kishnani, et al.. (2005). Triploid mosaicism in a 45,X/69,XXY infant. American Journal of Medical Genetics Part A. 138A(2). 171–174. 21 indexed citations

11.

Kalfa, Theodosia A., Sherri A. Zimmerman, Barbara K. Goodman, Marie McDonald, & Russell E. Ware. (2005). Pelger–Huët anomaly in a child with 1q42.3‐44 deletion. Pediatric Blood & Cancer. 46(5). 645–648. 3 indexed citations

12.

Sebastian, Siby, Timothy S. Collins, Carlos A Tirado, et al.. (2004). Molecular and cytogenetic characterization of a novel translocation t(4;22) involving the breakpoint cluster region and platelet‐derived growth factor receptor–alpha genes in a patient with atypical chronic myeloid leukemia. Genes Chromosomes and Cancer. 40(1). 44–50. 32 indexed citations

13.

Fang, Yanan, Barbara K. Goodman, Ryohei Furumai, et al.. (2004). ATR functions as a gene dosage‐dependent tumor suppressor on a mismatch repair‐deficient background. The EMBO Journal. 23(15). 3164–3174. 84 indexed citations

14.

Tirado, Carlos A, et al.. (2003). Cytogenetic and molecular analysis of an unusual case of acute promyelocytic leukemia with a t(15;17;)(q22;q23;q21). Cancer Genetics and Cytogenetics. 145(1). 31–37. 23 indexed citations

15.

Cargile, Colyn B., Denise Goh, Barbara K. Goodman, et al.. (2002). Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome. American Journal of Medical Genetics. 109(2). 133–138. 50 indexed citations

16.

Tuck‐Müller, Cathy M., Barbara K. Goodman, Shibo Li, et al.. (2001). Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel. Genetics in Medicine. 3(2). 126–131. 4 indexed citations

17.

Sacksteder, Katherine A., James C. Morrell, Barbara K. Goodman, et al.. (2000). Identification of the α-Aminoadipic Semialdehyde Synthase Gene, Which Is Defective in Familial Hyperlysinemia. The American Journal of Human Genetics. 66(6). 1736–1743. 78 indexed citations

18.

Goodman, Barbara K., et al.. (1997). Familial tandem duplication of bands q31.1 to q32.3 on chromosome 4 with mild phenotypic effect. American Journal of Medical Genetics. 73(2). 119–124. 26 indexed citations

19.

Goodman, Barbara K., Deborah Klein, David E. Tabor, et al.. (1994). Functional and molecular analysis of liver arginase promoter sequences from man andMacaca fascicularis. Somatic Cell and Molecular Genetics. 20(4). 313–325. 3 indexed citations

20.

Korenberg, Julie R., Lawrence D. Platt, Stephen L. Gans, et al.. (1991). Congenital gastric teratoma in Wiedemann‐Beckwith syndrome. American Journal of Medical Genetics. 38(1). 52–57. 17 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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