S. Hussain Askree

683 total citations
6 papers, 378 citations indexed

About

S. Hussain Askree is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, S. Hussain Askree has authored 6 papers receiving a total of 378 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Plant Science. Recurrent topics in S. Hussain Askree's work include Genetic Syndromes and Imprinting (2 papers), CRISPR and Genetic Engineering (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). S. Hussain Askree is often cited by papers focused on Genetic Syndromes and Imprinting (2 papers), CRISPR and Genetic Engineering (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). S. Hussain Askree collaborates with scholars based in United States and Israel. S. Hussain Askree's co-authors include Sarit Smolikov, Raya Gurevich, Joshua D. Hawk, Martin Kupiec, Anat Krauskopf, Michael J. McEachern, Madhuri Hegde, Kathryn B. Garber, Patricia Hall and Bradford Coffee and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genome Research and Genetics in Medicine.

In The Last Decade

S. Hussain Askree

6 papers receiving 375 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
S. Hussain Askree United States	5	311	126	64	56	55	6	378
Anne E. Dodson United States	9	467 1.5×	28 0.2×	45 0.7×	72 1.3×	117 2.1×	16	541
Taketo Taguchi United States	3	216 0.7×	74 0.6×	19 0.3×	93 1.7×	41 0.7×	5	325
Andrea Formenton Switzerland	6	508 1.6×	124 1.0×	49 0.8×	84 1.5×	25 0.5×	6	603
Muhammad Khairul Ramlee Singapore	6	213 0.7×	127 1.0×	30 0.5×	24 0.4×	20 0.4×	8	288
Nikolaos Charmpilas Greece	9	199 0.6×	35 0.3×	16 0.3×	12 0.2×	45 0.8×	13	272
Wing Lee Chan Germany	7	221 0.7×	19 0.2×	76 1.2×	36 0.6×	14 0.3×	7	289
Claudia Armenise France	9	390 1.3×	86 0.7×	76 1.2×	241 4.3×	31 0.6×	10	513
Patrick Gonzales United States	9	172 0.6×	47 0.4×	33 0.5×	34 0.6×	24 0.4×	13	286
Michael V. Zuccaro United States	10	403 1.3×	22 0.2×	137 2.1×	33 0.6×	23 0.4×	16	476
Chirag Jain Germany	5	213 0.7×	64 0.5×	67 1.0×	14 0.3×	92 1.7×	8	350

Countries citing papers authored by S. Hussain Askree

Since Specialization

Citations

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

Fields of papers citing papers by S. Hussain Askree

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. Hussain Askree. 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 S. Hussain Askree. The network helps show where S. Hussain Askree may publish in the future.

Co-authorship network of co-authors of S. Hussain Askree

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Garber, Kathryn B., et al.. (2016). Variants of uncertain significance in newborn screening disorders: implications for large-scale genomic sequencing. Genetics in Medicine. 19(1). 77–82. 28 indexed citations

2.

Askree, S. Hussain, Ephrem Chin, Lora Bean, et al.. (2013). Detection limit of intragenic deletions with targeted array comparative genomic hybridization. BMC Genetics. 14(1). 116–116. 14 indexed citations

3.

Askree, S. Hussain, et al.. (2012). Parent-of-Origin Testing for 15q11-q13 Gains by Quantitative DNA Methylation Analysis. Journal of Molecular Diagnostics. 14(3). 192–198. 4 indexed citations

4.

Ankala, Arunkanth, et al.. (2011). Aberrant firing of replication origins potentially explains intragenic nonrecurrent rearrangements within genes, including the human DMD gene. Genome Research. 22(1). 25–34. 41 indexed citations

5.

Askree, S. Hussain, Lawrence N. Hjelm, Muhammad Pervaiz, et al.. (2011). Allelic Dropout Can Cause False-Positive Results for Prader-Willi and Angelman Syndrome Testing. Journal of Molecular Diagnostics. 13(1). 108–112. 10 indexed citations

6.

Askree, S. Hussain, Sarit Smolikov, Raya Gurevich, et al.. (2004). A genome-wide screen for Saccharomyces cerevisiae deletion mutants that affect telomere length. Proceedings of the National Academy of Sciences. 101(23). 8658–8663. 281 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.

Explore authors with similar magnitude of impact