Diane Kissell

1.8k total citations
15 papers, 758 citations indexed

About

Diane Kissell is a scholar working on Infectious Diseases, Hematology and Immunology. According to data from OpenAlex, Diane Kissell has authored 15 papers receiving a total of 758 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Infectious Diseases, 5 papers in Hematology and 5 papers in Immunology. Recurrent topics in Diane Kissell's work include Parvovirus B19 Infection Studies (4 papers), Immune Cell Function and Interaction (4 papers) and Autoimmune and Inflammatory Disorders Research (4 papers). Diane Kissell is often cited by papers focused on Parvovirus B19 Infection Studies (4 papers), Immune Cell Function and Interaction (4 papers) and Autoimmune and Inflammatory Disorders Research (4 papers). Diane Kissell collaborates with scholars based in United States, United Kingdom and Pakistan. Diane Kissell's co-authors include Kejian Zhang, Alexandra H. Filipovich, Judith A. Johnson, Ammar Husami, Qian Wei, Peter S. Klein, Kimberly Risma, Michael B. Jordan, Jarek Meller and Joyce Villanueva and has published in prestigious journals such as Blood, Neurology and The Journal of Infectious Diseases.

In The Last Decade

Diane Kissell

14 papers receiving 749 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Diane Kissell United States	12	446	372	291	111	108	15	758
Valentina Cetica Italy	20	427 1.0×	384 1.0×	247 0.8×	217 2.0×	41 0.4×	33	917
Niansheng Chu United States	13	214 0.5×	394 1.1×	85 0.3×	103 0.9×	16 0.1×	21	580
Tania Cellucci Canada	12	64 0.1×	45 0.1×	98 0.3×	140 1.3×	542 5.0×	27	829
Julia O’Mahony Canada	16	79 0.2×	149 0.4×	37 0.1×	138 1.2×	325 3.0×	43	840
H. Link Germany	17	146 0.3×	373 1.0×	72 0.2×	118 1.1×	179 1.7×	41	862
Nobuko Yamashita Japan	14	71 0.2×	89 0.2×	123 0.4×	100 0.9×	174 1.6×	34	599
Laurie Zoecklein United States	14	106 0.2×	186 0.5×	42 0.1×	105 0.9×	73 0.7×	24	559
Cristina Ramo‐Tello Spain	19	47 0.1×	530 1.4×	39 0.1×	160 1.4×	197 1.8×	52	1.0k
Sophie Servais Belgium	16	348 0.8×	199 0.5×	59 0.2×	52 0.5×	27 0.3×	47	615
Jacov Levy Israel	17	79 0.2×	361 1.0×	19 0.1×	169 1.5×	47 0.4×	42	909

Countries citing papers authored by Diane Kissell

Since Specialization

Citations

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

Fields of papers citing papers by Diane Kissell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Diane Kissell

This figure shows the co-authorship network connecting the top 25 collaborators of Diane Kissell. A scholar is included among the top collaborators of Diane Kissell 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 Diane Kissell. Diane Kissell is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Lucky, Anne W., Neha Dagaonkar, Karen M. Lammers, et al.. (2018). A comprehensive next‐generation sequencing assay for the diagnosis of epidermolysis bullosa. Pediatric Dermatology. 35(2). 188–197. 23 indexed citations

Myers, Melanie F., Xue Zhang, Diane Kissell, et al.. (2017). Prior Opioid Exposure Influences Parents’ Sharing of Their Children’s CYP2D6 Research Results. Pharmacogenomics. 18(13). 1199–1213. 3 indexed citations

Teusink, Ashley, Alexander A. Vinks, Kejian Zhang, et al.. (2015). Genotype-Directed Dosing Leads to Optimized Voriconazole Levels in Pediatric Patients Receiving Hematopoietic Stem Cell Transplantation. Biology of Blood and Marrow Transplantation. 22(3). 482–486. 34 indexed citations

Jodele, Sonata, Benjamin L. Laskin, Kejian Zhang, et al.. (2015). The Genetic Fingerprint of Susceptibility to Transplant Associated Thrombotic Microangiopathy. Biology of Blood and Marrow Transplantation. 21(2). S98–S98. 14 indexed citations

Schulert, Grant S., Mingce Zhang, Ndate Fall, et al.. (2015). Whole-Exome Sequencing Reveals Mutations in Genes Linked to Hemophagocytic Lymphohistiocytosis and Macrophage Activation Syndrome in Fatal Cases of H1N1 Influenza. The Journal of Infectious Diseases. 213(7). 1180–1188. 115 indexed citations

Zhang, Kejian, Shanmuganathan Chandrakasan, Heather Chapman, et al.. (2014). Synergistic defects of different molecules in the cytotoxic pathway lead to clinical familial hemophagocytic lymphohistiocytosis. Blood. 124(8). 1331–1334. 99 indexed citations

Qian, Yaping, Judith A. Johnson, Jessica Connor, et al.. (2014). The 253‐kb inversion and deep intronic mutations in UNC13D are present in North American patients with familial hemophagocytic lymphohistiocytosis 3. Pediatric Blood & Cancer. 61(6). 1034–1040. 21 indexed citations

Begtrup, Amber, Neha Dagaonkar, Suvarnamala Pushkaran, et al.. (2013). Development Of a Comprehensive Rapid Next-Generation Sequencing Assay For The Diagnosis Of Inherited Hemolytic Anemia. Blood. 122(21). 949–949. 2 indexed citations

Sivakumaran, Theru A., Ammar Husami, Diane Kissell, et al.. (2013). Performance Evaluation of the Next‐Generation Sequencing Approach for Molecular Diagnosis of Hereditary Hearing Loss. Otolaryngology. 148(6). 1007–1016. 28 indexed citations

10.

Shahzad, Mohsin, Theru A. Sivakumaran, Julie M. Schultz, et al.. (2013). Genetic Analysis through OtoSeq of Pakistani Families Segregating Prelingual Hearing Loss. Otolaryngology. 149(3). 478–487. 19 indexed citations

11.

Kalfa, Theodosia A., Mary Risinger, Suvarnamala Pushkaran, et al.. (2012). Next Generation Sequencing for Diagnostic Testing of Erythrocyte Cytoskeleton Disorders. Blood. 120(21). 976–976.

12.

Zhang, Kejian, Michael B. Jordan, Rebecca Marsh, et al.. (2011). Hypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH. Blood. 118(22). 5794–5798. 288 indexed citations

13.

Simon, David K., Nathan Pankratz, Diane Kissell, et al.. (2010). Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease. BMC Medical Genetics. 11(1). 53–53. 26 indexed citations

14.

Nichols, William C., Diane Kissell, Nathan Pankratz, et al.. (2009). Variation in GIGYF2 is not associated with Parkinson disease. Neurology. 72(22). 1886–1892. 33 indexed citations

15.

Pankratz, Nathan, Diane Kissell, Michael W. Pauciulo, et al.. (2009). Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations. Neurology. 73(4). 279–286. 53 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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