Ivana Klisak

5.0k citations

67 papers · 4.0k indexed · 2 hit papers · h-index 27

Molecular Biology top 5%
Genetics top 2%
Immunology top 2%
Genetics top 1%
Surgery top 10%

Co-authors: Robert S. Sparkes T. Mohandas John E. Byfield Paula M. Calabro-Jones Shirley G. Quan David J. Rawlings R.Cutler Allen Douglas C. Saffran
Topics: Genomic variations and chromosomal abnormalities (10 papers)Chronic Lymphocytic Leukemia Research (7 papers)Genomics and Chromatin Dynamics (7 papers)
Cited by: Genetics Immunology
Journals: Science Cell The Lancet
Partner nations: United States Japan Germany

In The Last Decade

Ivana Klisak

67 papers receiving 3.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia

1993 1.1k citations Satoshi Tsukada, Douglas C. Saffran et al. Cell profile →
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

1993 527 citations Ethylin Wang Jabs, Ulrich Müller et al. Cell profile →

Peers

Countries citing papers authored by Ivana Klisak

Since Specialization

Citations

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

Fields of papers citing papers by Ivana Klisak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ivana Klisak

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

#	Work	Indexed citations
1	Pillars Article: Deficient Expression of a B Cell Cytoplasmic Tyrosine Kinase in Human X-linked Agammaglobulinemia. Cell. 1993. 72: 279–290 2012 ·The Journal of Immunology ·Satoshi Tsukada,Douglas C. Saffran,David J. Rawlings,Ornella Parolini,Roger C. Allen,Ivana Klisak,Robert S. Sparkes,Hiromi Kubagawa,T. Mohandas,Shirley G. Quan,John W. Belmont,Max D. Cooper,Mary Ellen Conley,Owen N. Witte	2
2	Localization of multiple human dihydrodiol dehydrogenase (DDH1 and DDH2) and chlordecone reductase (CHDR) genes in chromosome 10 by the polymerase chain reaction and fluorescence in situ hybridization 1995 ·Genomics ·Marilyn Khanna,Kenan Qin,Ivana Klisak,(unknown),Robert S. Sparkes,(unknown)	22
3	Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemiabreakdown → 1993 ·Cell ·Satoshi Tsukada,Douglas C. Saffran,David J. Rawlings,Ornella Parolini,R.Cutler Allen,Ivana Klisak,Robert S. Sparkes,Hiromi Kubagawa,T. Mohandas,Shirley G. Quan,John W. Belmont,Max D. Cooper,Mary Ellen Conley,Owen N. Witte	1053
4	A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosisbreakdown → 1993 ·Cell ·Ethylin Wang Jabs,Ulrich Müller,Xiang Li,Liang Ma,Wen Luo,Ian S. Haworth,Ivana Klisak,Robert S. Sparkes,Matthew L. Warman,John B. Mulliken,Malcolm L. Snead,Rob Maxson	527
5	The l-isoaspartyl/d-aspartyl protein methyltransferase gene (PCMT1) maps to human chromosome 6q22.3–6q24 and the syntenic region of mouse chromosome 10 1992 ·Genomics ·Duncan C. MacLaren,Clare M. O’Connor,Yu-Rong Xia,Margarete Mehrabian,Ivana Klisak,R.S. Sparkes,(unknown),(unknown)	12
6	Mapping of the gene for the cardiac sarcolemmal Na+Ca2+ exchanger to human chromosome 2p21–p23 1992 ·Genomics ·(unknown),Yu Xia,R S Sparkes,Ivana Klisak,Aldons J. Lusis,Debora A. Nicoll,Kenneth D. Philipson	19
7	The human retinal degeneration slow (RDS) gene: Chromosome assignment and structure of the mRNA 1991 ·Genomics ·Gabriel H. Travis,Lori B. Christerson,Patria E. Danielson,Ivana Klisak,Robert S. Sparkes,Lauri B. Hahn,Thaddeus P. Dryja,J. Gregor Sutcliffe	108
8	A U6 snRNA gene with an Internal promoter is juxtaposed to an snRNP protein sequence within an intron of a human G protein gene 1991 ·Nucleic Acids Research ·Eric D. Wieben,Anne M. Vrabel,Eileen L. Holicky,Ivana Klisak,Robert S. Sparkes,David R. Stanford	5
9	Assignment of the human gene for CREB1 to chromosome 2q32.3–q34 1990 ·Genomics ·Annette K. Taylor,Ivana Klisak,T. Mohandas,Robert S. Sparkes,Ching Li,Richard B. Gaynor,Aldons J. Lusis	28
10	Assignment of the gene for the small nuclear ribonucleoprotein E (SNRPE) to human chromosome 1q25–q43 1990 ·Genomics ·Katherine Neiswanger,David R. Stanford,R S Sparkes,Darryl Nishimura,T. Mohandas,Ivana Klisak,Camilla Heinzmann,Eric D. Wieben	6
11	Mapping of the gene for CNBP, a finger protein, to human chromosome 3q13.3–q24 1990 ·Genomics ·Aldons J. Lusis,T B Rajavashisth,Ivana Klisak,Camilla Heinzmann,T. Mohandas,R S Sparkes	11
12	Isolation and characterization of cDNA encoding the gamma-subunit of cGMP phosphodiesterase in human retina 1990 ·Gene ·Narendra Tuteja,Michael Danciger,Ivana Klisak,Renu Tuteja,George Inana,T. Mohandas,Robert S. Sparkes,Debora B. Farber	26
13	Chromosomal distribution of three members of the human natriuretic peptide receptor/guanylyl cyclase gene family 1990 ·Genomics ·David Lowe,Ivana Klisak,Robert S. Sparkes,T. Mohandas,David V. Goeddel	38
14	A gene homologous to plasminogen located on human chromosome 2q11–p11 1989 ·Genomics ·(unknown),Ivana Klisak,Robert S. Sparkes,Aldons J. Lusis	14
15	Human monoamine oxidase A and B genes map to xp11.23 and are deleted in a patient with norrie disease 1989 ·Genomics ·Nancy C. Lan,Camilla Heinzmann,Andreas Gal,Ivana Klisak,Ulrike Orth,Eric Lai,Joseph Grimsby,Robert S. Sparkes,T. Mohandas,Jean C. Shih	167
16	Human Aromatase: cDNA Cloning, Southern Blot Analysis, and Assignment of the Gene to Chromosome 15 1988 ·DNA ·Shiuan Chen,Marc J. Besman,Robert S. Sparkes,Susan Zollman,Ivana Klisak,T. Mohandas,Peter F. Hall,John E. Shively	188
17	The apolipoprotein(a) gene resides on human chromosome 6q26?27, in close proximity to the homologous gene for plasminogen 1988 ·Human Genetics ·(unknown),Ivana Klisak,(unknown),T. Mohandas,(unknown),(unknown),(unknown),(unknown)	103
18	Nucleotide Sequence for the cDNA of the Bovine βB2 Crystallin and Assignment of the Orthologous Human Locus to Chromosome 22 1987 ·Current Eye Research ·David Hogg,Michael B. Gorin,Camilla Heinzmann,Susan Zollman,T. Mohandas,Ivana Klisak,Robert S. Sparkes,Martin L. Breitman,L.-C. Tsui,Joseph Horwitz	30
19	Assignment of the human gene for cholesteryl ester transfer protein to chromosome 16q12–16q21 1987 ·Genomics ·Aldons J. Lusis,Susan Zollman,Robert S. Sparkes,Ivana Klisak,T. Mohandas,Dennis Drayna,Richard M. Lawn	27
20	Report of a trisomy 8p infant with carrier father. 1978 ·Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·(unknown),(unknown),Ivana Klisak	16

About Ivana Klisak

Ivana Klisak is a scholar working on Genetics, Genetics and Hematology, having authored 67 papers that have together received 4.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Chronic Lymphocytic Leukemia Research (7 papers) and Genomics and Chromatin Dynamics (7 papers). The work is most often cited by research in Genetics (703 citations), Immunology (1.0k citations) and Genetics (1.1k citations). Ivana Klisak has collaborated with scholars based in United States, Japan and Germany. Frequent co-authors include Robert S. Sparkes, T. Mohandas, John E. Byfield, Paula M. Calabro-Jones, T. Mohandas, Shirley G. Quan, David J. Rawlings, R.Cutler Allen, Douglas C. Saffran and Satoshi Tsukada. Their work appears in journals such as Science, Cell and The Lancet.

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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