Jeanette M. Ramos
Sourced from institutional research profiles (UAMS TRI or ARA).
Associate Professor
Faculty Researcher
Pathology, College of Medicine
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Jeanette M. Ramos's research focuses on the pathological mechanisms and diagnosis of various diseases, with a particular emphasis on infectious agents and hematological disorders. Her work has investigated fatal cases of *Naegleria fowleri* meningoencephalitis and severe tick-borne diseases in infants, exploring their role as triggers for syndromes like Hemophagocytic Lymphohistiocytosis (HLH). Dr. Ramos also examines less common causes of pancytopenia, differentiating them from malignant conditions, and has published on the diagnostic considerations for Acute Myeloid Leukemia with hemophagocytosis. Her research further includes an investigation into pulmonary saddle embolism linked to hypercoagulability from pancreatic cancer metastasis. She has a publication record of 21 papers, with an h-index of 6 and 95 total citations, and collaborates with researchers at the University of Arkansas for Medical Sciences, including Salim Aljabari, Steven Dahl, and Shahwar Yousuf.
Metrics
- h-index: 6
- Publications: 21
- Citations: 95
Selected Publications
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Severe transient abnormal myelopoiesis in a premature neonate with Trisomy 21: a rare, fatal presentation with complex therapeutic challenges (2026)
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Vascular Pathology: A Multifocal Cadaveric Analysis of Arterial Aneurysms (2025)
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Acute Myeloid Leukemia with Hemophagocytosis: Diagnostic Cues and Potential Pitfalls. (2025)PubMed OpenAlex
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Investigation of Pulmonary Saddle Embolism Caused by Metastasis-Induced Hypercoagulability Originating From Pancreatic Cancer (2024)
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828: FATAL TICK-BORNE DISEASE IN A VERY YOUNG INFANT: AN UNUSUAL DRIVER OF HLH-LIKE SYNDROME (2023)
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Fluorescent In Situ Hybridization (FISH) (2021)
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Unexpected and prominent parvovirus infection in a patient with plasma cell myeloma (2020)
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Hydatid Disease of the Urinary Bladder: a Review (2020)
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S1438 Epstein-Barr Virus Infection Masquerading as Cholestasis in a Patient With Gallstone Disease (2020)
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Plasma cell myeloma in a patient with Gaucher disease (2019)
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Late breast cancer recurrence with bone marrow metastases and acute pulmonary hypertension (2018)
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An unusual presentation of chronic lymphocytic leukemia (2017)
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The utility of B-cell receptor gene rearrangement studies in diagnosing diffuse large B-cell lymphoma with plasmacytic differentiation. (2015)
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An Unusual Case of Gastric Cancer with Bone Marrow Metastases and Embolic Phenomena as Initial Presentation (2015)
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First Reported Case of Ehrlichia ewingii Involving Human Bone Marrow (2014)
Collaboration Network
Top Collaborators
- Vascular Pathology: A Multifocal Cadaveric Analysis of Arterial Aneurysms
- Vascular Pathology: A Multifocal Cadaveric Analysis of Arterial Aneurysms
- Vascular Pathology: A Multifocal Cadaveric Analysis of Arterial Aneurysms
- Vascular Pathology: A Multifocal Cadaveric Analysis of Arterial Aneurysms
- Vascular Pathology: A Multifocal Cadaveric Analysis of Arterial Aneurysms
- Vascular Pathology: A Multifocal Cadaveric Analysis of Arterial Aneurysms
- Vascular Pathology: A Multifocal Cadaveric Analysis of Arterial Aneurysms
- Vascular Pathology: A Multifocal Cadaveric Analysis of Arterial Aneurysms
- Vascular Pathology: A Multifocal Cadaveric Analysis of Arterial Aneurysms
- Vascular Pathology: A Multifocal Cadaveric Analysis of Arterial Aneurysms
- Vascular Pathology: A Multifocal Cadaveric Analysis of Arterial Aneurysms
- Severe transient abnormal myelopoiesis in a premature neonate with Trisomy 21: a rare, fatal presentation with complex therapeutic challenges
- Severe transient abnormal myelopoiesis in a premature neonate with Trisomy 21: a rare, fatal presentation with complex therapeutic challenges
- Severe transient abnormal myelopoiesis in a premature neonate with Trisomy 21: a rare, fatal presentation with complex therapeutic challenges
- Severe transient abnormal myelopoiesis in a premature neonate with Trisomy 21: a rare, fatal presentation with complex therapeutic challenges
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