Ammar Husami

2.7k total citations
28 papers, 748 citations indexed

About

Ammar Husami is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Ammar Husami has authored 28 papers receiving a total of 748 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 10 papers in Molecular Biology and 7 papers in Hematology. Recurrent topics in Ammar Husami's work include Genomics and Rare Diseases (8 papers), Autoimmune and Inflammatory Disorders Research (6 papers) and Immune Cell Function and Interaction (4 papers). Ammar Husami is often cited by papers focused on Genomics and Rare Diseases (8 papers), Autoimmune and Inflammatory Disorders Research (6 papers) and Immune Cell Function and Interaction (4 papers). Ammar Husami collaborates with scholars based in United States, India and China. Ammar Husami's co-authors include Kejian Zhang, Alexei A. Grom, Diane Kissell, Alexandra H. Filipovich, Ndate Fall, Grant S. Schulert, C. Alexander Valencia, Judith A. Johnson, Kenneth M. Kaufman and John B. Harley and has published in prestigious journals such as Blood, Gastroenterology and PLoS ONE.

In The Last Decade

Ammar Husami

24 papers receiving 743 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ammar Husami United States 14 424 285 161 157 142 28 748
Halima Moncrieffe United Kingdom 16 472 1.1× 579 2.0× 27 0.2× 291 1.9× 87 0.6× 24 1.1k
Jingshi Wang China 18 482 1.1× 425 1.5× 290 1.8× 254 1.6× 54 0.4× 96 915
Rita Clementi Italy 13 505 1.2× 528 1.9× 265 1.6× 59 0.4× 36 0.3× 21 821
Jasmin Kümmerle‐Deschner Germany 13 222 0.5× 194 0.7× 18 0.1× 206 1.3× 82 0.6× 35 627
Niansheng Chu United States 13 214 0.5× 394 1.4× 85 0.5× 103 0.7× 71 0.5× 21 580
Rémi Dufourcq-Lagelouse France 7 943 2.2× 800 2.8× 493 3.1× 278 1.8× 58 0.4× 8 1.4k
Bianca Tesi Sweden 14 229 0.5× 843 3.0× 94 0.6× 119 0.8× 38 0.3× 43 1.1k
Arpita Myles United States 16 118 0.3× 596 2.1× 48 0.3× 203 1.3× 38 0.3× 23 905
D. Kingsbury United States 13 217 0.5× 235 0.8× 16 0.1× 243 1.5× 36 0.3× 25 768
Eduardo Cuende Spain 13 72 0.2× 231 0.8× 38 0.2× 154 1.0× 52 0.4× 32 590

Countries citing papers authored by Ammar Husami

Since Specialization
Citations

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

Fields of papers citing papers by Ammar Husami

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ammar Husami

This figure shows the co-authorship network connecting the top 25 collaborators of Ammar Husami. A scholar is included among the top collaborators of Ammar Husami 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 Ammar Husami. Ammar Husami 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.
Husami, Ammar, et al.. (2025). Genetic analysis and functional assessment of a TGFBR2 variant in micrognathia and cleft palate. PLoS ONE. 20(6). e0324803–e0324803.
2.
Yang, Zeyu, Amy Shikany, Ammar Husami, et al.. (2025). Sequencing validates deep learning models for EHR-based detection of Noonan syndrome in pediatric patients. npj Genomic Medicine. 10(1). 56–56.
3.
Dolin, Robert H., et al.. (2025). Genetic data normalization for genomic medicine: a Fast Healthcare Interoperability Resources Genomics reference implementation. Journal of the American Medical Informatics Association. 32(10). 1598–1608.
4.
Dolin, Robert H., Bret S.E. Heale, Carla Álvarez, et al.. (2023). Sync for Genes Phase 5: Computable artifacts for sharing dynamically annotated FHIR‐formatted genomic variants. Learning Health Systems. 7(4). 3 indexed citations
5.
Baker, Elizabeth, Ben Pode‐Shakked, Laura Cross, et al.. (2022). PPP2R1A neurodevelopmental disorder is associated with congenital heart defects. American Journal of Medical Genetics Part A. 188(11). 3262–3277. 7 indexed citations
6.
Simpson, Brittany, Ammar Husami, Valentina Pilipenko, et al.. (2022). The 2019–2020 Dengue Fever Epidemic: Genomic Markers Indicating Severity in Dominican Republic Children. Journal of the Pediatric Infectious Diseases Society. 12(3). 169–172. 3 indexed citations
7.
Dolin, Robert H., Bret S.E. Heale, Gil Alterovitz, et al.. (2022). Introducing HL7 FHIR Genomics Operations: a developer-friendly approach to genomics-EHR integration. Journal of the American Medical Informatics Association. 30(3). 485–493. 19 indexed citations
8.
Dolin, Robert H., Aziz A. Boxwala, Bret S.E. Heale, et al.. (2021). vcf2fhir: a utility to convert VCF files into HL7 FHIR format for genomics-EHR integration. BMC Bioinformatics. 22(1). 104–104. 14 indexed citations
9.
Pham, Duc-Hung, Lingfen Xu, C. Alexander Valencia, et al.. (2021). Deleterious Variants in ABCC12 are Detected in Idiopathic Chronic Cholestasis and Cause Intrahepatic Bile Duct Loss in Model Organisms. Gastroenterology. 161(1). 287–300.e16. 14 indexed citations
10.
Schulert, Grant S., Shima Yasin, Brenna Carey, et al.. (2019). Systemic Juvenile Idiopathic Arthritis–Associated Lung Disease: Characterization and Risk Factors. Arthritis & Rheumatology. 71(11). 1943–1954. 115 indexed citations
11.
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
12.
Abu‐El‐Haija, Maisam, Lindsey Hornung, Lee A. Denson, et al.. (2018). Prevalence of abnormal glucose metabolism in pediatric acute, acute recurrent and chronic pancreatitis. PLoS ONE. 13(10). e0204979–e0204979. 21 indexed citations
13.
Schulert, Grant S., Mingce Zhang, Ammar Husami, et al.. (2018). Brief Report: Novel UNC13D Intronic Variant Disrupting an NF‐κB Enhancer in a Patient With Recurrent Macrophage Activation Syndrome and Systemic Juvenile Idiopathic Arthritis. Arthritis & Rheumatology. 70(6). 963–970. 33 indexed citations
14.
Valencia, C. Alexander, Abhinav Mathur, Chao Wei, et al.. (2018). CCEPAS: the creation and validation of a fast and sensitive clinical whole exome analysis pipeline based on gene and variant ranking. 2. 1–1. 1 indexed citations
15.
Valencia, C. Alexander, Xinjian Wang, Jin Wang, et al.. (2016). Deep Sequencing Reveals Novel Genetic Variants in Children with Acute Liver Failure and Tissue Evidence of Impaired Energy Metabolism. PLoS ONE. 11(8). e0156738–e0156738. 9 indexed citations
16.
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
17.
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
18.
Kottyan, Leah C., Marc S. Williams, David H. Ledbetter, et al.. (2014). The struggle to find reliable results in exome sequencing data: filtering out Mendelian errors. Frontiers in Genetics. 5. 16–16. 31 indexed citations
19.
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.
20.
Kothiyal, Prachi, Stephanie Cox, Ammar Husami, et al.. (2010). High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays. BMC Biotechnology. 10(1). 10–10. 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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