Imran S. Haque

5.6k total citations · 2 hit papers
46 papers, 3.5k citations indexed

About

Imran S. Haque is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Imran S. Haque has authored 46 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 15 papers in Genetics and 10 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Imran S. Haque's work include Cystic Fibrosis Research Advances (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Protein Structure and Dynamics (7 papers). Imran S. Haque is often cited by papers focused on Cystic Fibrosis Research Advances (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Protein Structure and Dynamics (7 papers). Imran S. Haque collaborates with scholars based in United States, Germany and France. Imran S. Haque's co-authors include Charles E. S. Roberts, Michael R. Speicher, Ellen Heitzer, Vijay S. Pande, Gabriel A. Lazarin, Chuanjie Wu, Pengyu Ren, Gary N. I. Clark, Martin Head‐Gordon and Michael J. Schnieders and has published in prestigious journals such as JAMA, The Journal of Chemical Physics and Nature Genetics.

In The Last Decade

Imran S. Haque

41 papers receiving 3.4k 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.

Current Status of the AMOEBA Polarizable Force Field

2010 1.1k citations Jay W. Ponder, Chuanjie Wu et al. The Journal of Physical Chemistry B profile →
Current and future perspectives of liquid biopsies in genomics-driven oncology

2018 948 citations Ellen Heitzer, Imran S. Haque et al. Nature Reviews Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Imran S. Haque United States	20	1.6k	718	668	629	453	46	3.5k
A. Zaslavsky United States	39	1.4k 0.9×	423 0.6×	337 0.5×	1.1k 1.7×	712 1.6×	197	5.7k
Shoudan Liang United States	35	3.5k 2.2×	554 0.8×	235 0.4×	337 0.5×	256 0.6×	84	5.5k
Simon P. Robinson United Kingdom	49	2.0k 1.3×	1.7k 2.4×	859 1.3×	261 0.4×	573 1.3×	243	8.1k
Jörg Steinbach Germany	43	2.6k 1.6×	942 1.3×	834 1.2×	445 0.7×	239 0.5×	305	7.4k
David Lucas United States	44	2.6k 1.6×	251 0.3×	391 0.6×	1.9k 3.1×	123 0.3×	279	7.7k
Joseph Beechem United States	47	5.3k 3.3×	451 0.6×	401 0.6×	634 1.0×	1.2k 2.7×	145	7.6k
Robert A. Beckman United States	33	1.8k 1.1×	662 0.9×	254 0.4×	193 0.3×	362 0.8×	113	3.7k
Christopher A. Reynolds United Kingdom	41	2.5k 1.6×	345 0.5×	255 0.4×	576 0.9×	345 0.8×	168	5.2k
Maneesh Jain United States	50	3.8k 2.4×	1.1k 1.5×	750 1.1×	1.1k 1.7×	137 0.3×	153	7.8k
Philip Walther United States	50	770 0.5×	570 0.8×	1.6k 2.4×	4.7k 7.5×	219 0.5×	221	9.8k

Countries citing papers authored by Imran S. Haque

Since Specialization

Citations

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

Fields of papers citing papers by Imran S. Haque

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Imran S. Haque

This figure shows the co-authorship network connecting the top 25 collaborators of Imran S. Haque. A scholar is included among the top collaborators of Imran S. Haque 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 Imran S. Haque. Imran S. Haque 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:

20 of 20 papers shown

Çelik, Safiye, et al.. (2024). Building, benchmarking, and exploring perturbative maps of transcriptional and morphological data. PLoS Computational Biology. 20(10). e1012463–e1012463. 5 indexed citations

Cho, Jin‐Gun, Liza Thomas, Jennifer Curnow, et al.. (2024). Pulmonary embolism response teams. A description of the first 36‐month Australian experience. Australasian Journal of Paramedicine. 54(8). 1283–1291.

Lazar, Nathan H., Safiye Çelik, Lu Chen, et al.. (2024). High-resolution genome-wide mapping of chromosome-arm-scale truncations induced by CRISPR–Cas9 editing. Nature Genetics. 56(7). 1482–1493. 19 indexed citations

Kaseniit, Kristjan Eerik, Imran S. Haque, Judith D. Goldberg, L.P. Shulman, & Dale Muzzey. (2020). Genetic ancestry analysis on >93,000 individuals undergoing expanded carrier screening reveals limitations of ethnicity-based medical guidelines. Genetics in Medicine. 22(10). 1694–1702. 49 indexed citations

Hogan, Gregory J., Valentina Vysotskaia, Kyle A. Beauchamp, et al.. (2018). Validation of an Expanded Carrier Screen that Optimizes Sensitivity via Full-Exon Sequencing and Panel-wide Copy Number Variant Identification. Clinical Chemistry. 64(7). 1063–1073. 46 indexed citations

Heitzer, Ellen, Imran S. Haque, Charles E. S. Roberts, & Michael R. Speicher. (2018). Current and future perspectives of liquid biopsies in genomics-driven oncology. Nature Reviews Genetics. 20(2). 71–88. 948 indexed citations breakdown →

Amorim, Carlos Eduardo G., Ziyue Gao, Yuval B. Simons, et al.. (2017). The population genetics of human disease: The case of recessive, lethal mutations. PLoS Genetics. 13(9). e1006915–e1006915. 31 indexed citations

Beauchamp, Kyle A., Dale Muzzey, Kenny K. Wong, et al.. (2017). Systematic design and comparison of expanded carrier screening panels. Genetics in Medicine. 20(1). 55–63. 45 indexed citations

Evans, Eric A., et al.. (2017). Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods. Prenatal Diagnosis. 37(5). 482–490. 22 indexed citations

10.

Lazarin, Gabriel A., Imran S. Haque, Eric A. Evans, & Judith D. Goldberg. (2017). Smith–Lemli–Opitz syndrome carrier frequency and estimates of in utero mortality rates. Prenatal Diagnosis. 37(4). 350–355. 28 indexed citations

11.

Goldberg, Judith D., et al.. (2017). Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At‐Risk Couples. Journal of Genetic Counseling. 27(3). 616–625. 64 indexed citations

12.

Wong, Kenny K., Judith D. Goldberg, Eric Evans, Hyunseok P. Kang, & Imran S. Haque. (2016). Re: Carrier Screening is a Deficient Strategy for Determining Sperm Donor Eligibility and Reducing Risk of Disease in Recipient Children(From: Silver AJ, Larson JL, Silver MJ, et al. Genet Test Mol Biomarkers 2016;20:276–284). Genetic Testing and Molecular Biomarkers. 20(8). 413–414. 1 indexed citations

13.

Mehta, Nikita, Gabriel A. Lazarin, Erica Spiegel, et al.. (2016). Tay-Sachs Carrier Screening by Enzyme and Molecular Analyses in the New York City Minority Population. Genetic Testing and Molecular Biomarkers. 20(9). 504–509. 4 indexed citations

14.

Kang, Hyunseok P., Jared Maguire, Clement Chu, et al.. (2016). Design and validation of a next generation sequencing assay for hereditary BRCA1 and BRCA2 mutation testing. PeerJ. 4. e2162–e2162. 13 indexed citations

15.

Lazarin, Gabriel A., et al.. (2014). Systematic Classification of Disease Severity for Evaluation of Expanded Carrier Screening Panels. PLoS ONE. 9(12). e114391–e114391. 102 indexed citations

16.

Lazarin, Gabriel A., Imran S. Haque, Shivani Nazareth, et al.. (2012). An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals. Genetics in Medicine. 15(3). 178–186. 188 indexed citations

17.

Haque, Imran S., Vijay S. Pande, & W. Patrick Walters. (2011). Anatomy of High-Performance 2D Similarity Calculations. Journal of Chemical Information and Modeling. 51(9). 2345–2351. 27 indexed citations

18.

Ready, Kaylene, Imran S. Haque, Balaji S. Srinivasan, & J. R. Marshall. (2011). Knowledge and attitudes regarding expanded genetic carrier screening among women’s healthcare providers. Fertility and Sterility. 97(2). 407–413. 37 indexed citations

19.

Haque, Imran S. & Vijay S. Pande. (2011). Error Bounds on the SCISSORS Approximation Method. Journal of Chemical Information and Modeling. 51(9). 2248–2253. 3 indexed citations

20.

Ponder, Jay W., Chuanjie Wu, Pengyu Ren, et al.. (2010). Current Status of the AMOEBA Polarizable Force Field. The Journal of Physical Chemistry B. 114(8). 2549–2564. 1096 indexed citations breakdown →

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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