K Richkind

915 total citations
30 papers, 605 citations indexed

About

K Richkind is a scholar working on Hematology, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, K Richkind has authored 30 papers receiving a total of 605 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Hematology, 11 papers in Molecular Biology and 8 papers in Pulmonary and Respiratory Medicine. Recurrent topics in K Richkind's work include Acute Myeloid Leukemia Research (11 papers), Sarcoma Diagnosis and Treatment (8 papers) and Acute Lymphoblastic Leukemia research (5 papers). K Richkind is often cited by papers focused on Acute Myeloid Leukemia Research (11 papers), Sarcoma Diagnosis and Treatment (8 papers) and Acute Lymphoblastic Leukemia research (5 papers). K Richkind collaborates with scholars based in United States, France and Australia. K Richkind's co-authors include Michael A. Bell, Jerry Z. Finklestein, Stephen G. Romansky, Eduardo Zambrano, Antonio R. Pérez‐Atayde, Sara O. Vargas, Harry P. Kozakewich, Robert Hromas, Marileila Varella‐Garcia and Humberto Vidaillet and has published in prestigious journals such as JAMA, Blood and The American Naturalist.

In The Last Decade

K Richkind

30 papers receiving 586 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
K Richkind United States 15 179 168 159 144 129 30 605
Hon Fong L. Mark United States 15 107 0.6× 44 0.3× 263 1.7× 237 1.6× 89 0.7× 54 668
Claudio Panarello Italy 12 87 0.5× 107 0.6× 182 1.1× 88 0.6× 193 1.5× 30 455
Hasan Acar Türkiye 12 75 0.4× 94 0.6× 139 0.9× 82 0.6× 42 0.3× 69 429
Ilse Chudoba Germany 16 171 1.0× 35 0.2× 436 2.7× 410 2.8× 91 0.7× 36 858
Brandon M. Shearer United States 11 137 0.8× 304 1.8× 113 0.7× 66 0.5× 145 1.1× 13 623
Emanuela Maserati Italy 21 49 0.3× 78 0.5× 332 2.1× 486 3.4× 423 3.3× 60 1.1k
C. Cullinane United Kingdom 19 378 2.1× 81 0.5× 428 2.7× 81 0.6× 33 0.3× 33 1.0k
Shaoxiong Chen United States 15 200 1.1× 111 0.7× 108 0.7× 43 0.3× 29 0.2× 64 621
L Koulischer Belgium 19 192 1.1× 69 0.4× 276 1.7× 386 2.7× 118 0.9× 94 1.1k
Paul D. Garen United States 16 110 0.6× 133 0.8× 228 1.4× 46 0.3× 8 0.1× 22 755

Countries citing papers authored by K Richkind

Since Specialization
Citations

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

Fields of papers citing papers by K Richkind

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K Richkind

This figure shows the co-authorship network connecting the top 25 collaborators of K Richkind. A scholar is included among the top collaborators of K Richkind 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 K Richkind. K Richkind 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.
Agoston, Agoston T., Cher‐Wei Liang, K Richkind, Jonathan A. Fletcher, & Sara O. Vargas. (2010). Trisomy 18 is a consistent cytogenetic feature in pilomatricoma. Modern Pathology. 23(8). 1147–1150. 13 indexed citations
2.
Kenney, Barton, K Richkind, & Eduardo Zambrano. (2007). Solid variant of aneurysmal bone cyst with a novel (X;9) translocation. Cancer Genetics and Cytogenetics. 178(2). 155–159. 11 indexed citations
3.
Kenney, Barton, K Richkind, Gary E. Friedlaender, & Eduardo Zambrano. (2007). Chromosomal rearrangements in lipofibromatosis. Cancer Genetics and Cytogenetics. 179(2). 136–139. 19 indexed citations
4.
Brock, Jane E., Antonio R. Pérez‐Atayde, Harry P. Kozakewich, et al.. (2005). Cytogenetic Aberrations in Perineurioma. The American Journal of Surgical Pathology. 29(9). 1164–1169. 45 indexed citations
5.
Zambrano, Eduardo, Vânia Nosé, Antonio R. Pérez‐Atayde, et al.. (2004). Distinct Chromosomal Rearrangements in Subungual (Dupuytren) Exostosis and Bizarre Parosteal Osteochondromatous Proliferation (Nora Lesion). The American Journal of Surgical Pathology. 28(8). 1033–1039. 58 indexed citations
6.
Chan, Edward M., Frank Brown, K Richkind, et al.. (2004). AML1-FOG2 Fusion Protein in Myelodysplasia.. Blood. 104(11). 2900–2900. 2 indexed citations
7.
Richkind, K, et al.. (2002). Translocation (16;20)(p11.2;q13). Cancer Genetics and Cytogenetics. 137(2). 153–155. 14 indexed citations
8.
Varella‐Garcia, Marileila, Joyce Murata‐Collins, K Richkind, et al.. (2001). Minimal residual disease (MRD) in remission t(8;21) AML and in vivo differentiation detected by FISH and CD34+ cell sorting. Leukemia. 15(9). 1408–1414. 15 indexed citations
9.
Hromas, Robert, et al.. (2001). Fusion AML1 transcript in a radiation-associated leukemia results in a truncated inhibitory AML1 protein. Blood. 97(7). 2168–2170. 31 indexed citations
10.
Richkind, K, et al.. (2000). Identification of two new translocations that disrupt the AML1 gene. Cancer Genetics and Cytogenetics. 122(2). 141–143. 21 indexed citations
11.
Morgan, Rodman, et al.. (1999). PHA/IL2. Cancer Genetics and Cytogenetics. 109(2). 134–137. 14 indexed citations
12.
Paskulin, Giorgio Adriano, George Philips, Rodman Morgan, et al.. (1998). Pre-clinical evaluation of probes to detect t(8;21) AML minimal residual disease by fluorescence in situ hybridization. Genes Chromosomes and Cancer. 21(2). 144–151. 15 indexed citations
13.
Hsu, Lillian Y. F., K Richkind, Daniel L. Van Dyke, et al.. (1996). INCIDENCE AND SIGNIFICANCE OF CHROMOSOME MOSAICISM INVOLVING AN AUTOSOMAL STRUCTURAL ABNORMALITY DIAGNOSED PRENATALLY THROUGH AMNIOCENTESIS: A COLLABORATIVE STUDY. Prenatal Diagnosis. 16(1). 1–28. 80 indexed citations
14.
Richkind, K, Stephen G. Romansky, & Jerry Z. Finklestein. (1996). t(4;19)(q35;q13.1): A recurrent change in primitive mesenchymal tumors?. Cancer Genetics and Cytogenetics. 87(1). 71–74. 58 indexed citations
15.
Richkind, K, et al.. (1994). Cardiac myxoma characterized by clonal telomeric association. Genes Chromosomes and Cancer. 9(1). 68–71. 26 indexed citations
16.
Richkind, K, et al.. (1992). The use of giant cell tumor conditioned media in cytogenetic studies of hematologic malignancies. Cancer Genetics and Cytogenetics. 61(2). 126–130. 8 indexed citations
17.
Richkind, K, et al.. (1991). Prenatal diagnosis and outcomes of five cases of mosaicism for an isochromosome of 20q. Prenatal Diagnosis. 11(6). 371–376. 7 indexed citations
18.
Richkind, K & Neil Risch. (1990). Sensitivity of chromosomal mosaicism detection by different tissue culture methods. Prenatal Diagnosis. 10(8). 519–527. 10 indexed citations
19.
Richkind, K, et al.. (1989). Translocation 1;7 in four cases of myeloid disorders. Cancer Genetics and Cytogenetics. 38(1). 49–52. 3 indexed citations
20.
Bell, Michael A. & K Richkind. (1981). Clinal Variation of Lateral Plates in Threespine Stickleback Fish. The American Naturalist. 117(2). 113–132. 42 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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