Alia Ahmed

548 citations

37 papers · 349 indexed · h-index 12

Co-authors: Chester B. Whitley Elsa Shapiro Igor Nestrašil Kathleen Delaney Kyle Rudser Brianna Yund Michael Potegal Alicia Kunin‐Batson
Topics: Lysosomal Storage Disorders Research (26 papers)Glycogen Storage Diseases and Myoclonus (11 papers)Child Nutrition and Feeding Issues (4 papers)
Cited by: Physiology Rheumatology Psychiatry and Mental health
Journals: Genetics in Medicine Journal of Clinical and Experimental Neuropsychology Molecular Genetics and Metabolism
Partner nations: United States Canada Germany

In The Last Decade

Alia Ahmed

34 papers receiving 342 citations

Peers

Countries citing papers authored by Alia Ahmed

Since Specialization

Citations

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

Fields of papers citing papers by Alia Ahmed

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alia Ahmed

This figure shows the co-authorship network connecting the top 25 collaborators of Alia Ahmed. A scholar is included among the top collaborators of Alia Ahmed 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 Alia Ahmed. Alia Ahmed 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	Pegvaliase therapy for phenylketonuria: Real-world safety, efficacy, and medication access outcomes in a pharmacist-led pegvaliase program 2025 ·Genetics in Medicine ·(unknown),Alicia Zagel,Nishitha R. Pillai,Alia Ahmed,Jon A. Jacobson,(unknown),Chester B. Whitley,(unknown)	1
2	Dose-intensive therapy (DIT) for infantile Pompe disease: A pilot study 2024 ·Molecular Genetics and Metabolism Reports ·(unknown),Nishitha R. Pillai,Alia Ahmed,(unknown),Michael J. Stark,Chester B. Whitley	0
3	Disparities in late and lost: Pediatricians' role in following Pompe disease identified by newborn screening 2023 ·Molecular Genetics and Metabolism ·Nishitha R. Pillai,(unknown),(unknown),(unknown),Alia Ahmed,Amy Hietala,Alissa Jorgenson,Brendan C. Lanpher,Chester B. Whitley	2
4	Quantifying medical manifestations in Hurler syndrome with the infant physical symptom score: associations with long-term physical and adaptive outcomes 2022 ·Molecular Genetics and Metabolism ·Alia Ahmed,Kyle Rudser,Kelly King,Julie B. Eisengart,Paul J. Orchard,Elsa Shapiro,Chester B. Whitley	0
5	Early Neonatal Cardiac Phenotype in Hurler Syndrome: Case Report and Literature Review 2022 ·Genes ·Nishitha R. Pillai,Alia Ahmed,(unknown),Chester B. Whitley	3
6	A longitudinal study of neurocognition and behavior in patients with Hurler-Scheie syndrome heterozygous for the L238Q mutation 2019 ·Molecular Genetics and Metabolism Reports ·Alia Ahmed,Li Ou,Kyle Rudser,Elsa Shapiro,Julie B. Eisengart,Kelly King,Agnes Chen,Patricia Dickson,Chester B. Whitley	4
7	Distinct progression patterns of brain disease in infantile and juvenile gangliosidoses: Volumetric quantitative MRI study 2017 ·Molecular Genetics and Metabolism ·Igor Nestrašil,Alia Ahmed,(unknown),Kyle Rudser,Chester B. Whitley,(unknown)	32
8	Long-term cognitive and somatic outcomes of enzyme replacement therapy in untransplanted Hurler syndrome 2017 ·Molecular Genetics and Metabolism Reports ·Julie B. Eisengart,(unknown),Alia Ahmed,Igor Nestrašil,Richard Ziegler,Kathleen Delaney,Elsa Shapiro,Chester B. Whitley	18
9	Observing the advanced disease course in mucopolysaccharidosis, type IIIA; a case series 2017 ·Molecular Genetics and Metabolism ·Elsa Shapiro,Alia Ahmed,Chester B. Whitley,Kathleen Delaney	16
10	A longitudinal study of emotional adjustment, quality of life and adaptive function in attenuated MPS II 2016 ·Molecular Genetics and Metabolism Reports ·Elsa Shapiro,Kyle Rudser,Alia Ahmed,Robert D. Steiner,Kathleen Delaney,Brianna Yund,Kelly King,Alicia Kunin‐Batson,Julie B. Eisengart,Chester B. Whitley	30
11	Association of somatic burden of disease with age and neuropsychological measures in attenuated mucopolysaccharidosis types I, II and VI 2016 ·Molecular Genetics and Metabolism Reports ·Alia Ahmed,Elsa Shapiro,Kyle Rudser,Alicia Kunin‐Batson,Kelly King,Chester B. Whitley	19
12	The neurobehavioral phenotype in mucopolysaccharidosis Type IIIB: An exploratory study 2016 ·Molecular Genetics and Metabolism Reports ·Elsa Shapiro,Kelly King,Alia Ahmed,Kyle Rudser,(unknown),Brianna Yund,Kathleen Delaney,Igor Nestrašil,C B Whitley,Michael Potegal	34
13	Mucopolysaccharidosis (MPS) Physical Symptom Score: Development, Reliability, and Validity 2015 ·JIMD Reports ·Alia Ahmed,Kyle Rudser,Alicia Kunin‐Batson,Kathleen Delaney,C B Whitley,Elsa Shapiro	6
14	Quantifying behaviors of children with Sanfilippo syndrome: The Sanfilippo Behavior Rating Scale 2015 ·Molecular Genetics and Metabolism ·Elsa Shapiro,Igor Nestrašil,Alia Ahmed,Andrew Wey,Kyle Rudser,Kathleen Delaney,(unknown),Patrick Haslett,Chester B. Whitley,Michael Potegal	33
15	Cognitive, medical, and neuroimaging characteristics of attenuated mucopolysaccharidosis type II 2014 ·Molecular Genetics and Metabolism ·Brianna Yund,Kyle Rudser,Alia Ahmed,(unknown),Igor Nestrašil,Julian Raiman,Eva Mamak,Paul Harmatz,Robert D. Steiner,Heather Lau,(unknown),Jeffrey R. Wozniak,Kelvin O. Lim,Kathleen Delaney,Chester B. Whitley,Elsa Shapiro	39
16	The MPS health assessment questionnaire: preliminary normative and validity data 2014 ·Molecular Genetics and Metabolism ·(unknown),Alia Ahmed,Brianna Yund,Chester B. Whitley,Elsa Shapiro	1
17	Neurocognitive and neuropsychiatric phenotypes associated with the mutation L238Q of the α-L-iduronidase gene in Hurler–Scheie syndrome 2013 ·Molecular Genetics and Metabolism ·Alia Ahmed,Chester B. Whitley,(unknown),Kyle Rudser,Stephanie Cagle,Nadia Ali,Kathleen Delaney,Brianna Yund,Elsa Shapiro	24
18	Mucopolysaccharidosis Type IIIA presents as a variant of Klüver–Bucy syndrome 2013 ·Journal of Clinical and Experimental Neuropsychology ·Michael Potegal,Brianna Yund,Kyle Rudser,Alia Ahmed,(unknown),Igor Nestrašil,Chester B. Whitley,Elsa Shapiro	26
19	Longitudinal studies of brain structure and function in MPS disorders: A study of the Lysosomal Disease network 2011 ·Molecular Genetics and Metabolism ·Elsa Shapiro,Julie B. Eisengart,Igor Nestrašil,Alia Ahmed,Julian Raiman,(unknown),Paul Harmatz,Gerald J. Berry,Gregory M. Pastores,Paul M. Fernhoff,David Viskochil,Kathleen Delaney	0
20	5. Reliability of manual and automated tracing of hippocampal volumes in MPS patients and normal controls: A report of the neuroimaging core of the lysosomal disease network 2010 ·Molecular Genetics and Metabolism ·Alia Ahmed,Igor Nestrašil,Kyle Rudser,Elsa Shapiro	3

About Alia Ahmed

Alia Ahmed is a scholar working on Physiology, Rheumatology and Anatomy, having authored 37 papers that have together received 349 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (26 papers), Glycogen Storage Diseases and Myoclonus (11 papers) and Child Nutrition and Feeding Issues (4 papers). The work is most often cited by research in Physiology (282 citations), Rheumatology (80 citations) and Psychiatry and Mental health (63 citations). Alia Ahmed has collaborated with scholars based in United States, Canada and Germany. Frequent co-authors include Chester B. Whitley, Elsa Shapiro, Igor Nestrašil, Kathleen Delaney, Kyle Rudser, Brianna Yund, Kyle Rudser, Michael Potegal, Alicia Kunin‐Batson and Kelly King. Their work appears in journals such as Genetics in Medicine, Journal of Clinical and Experimental Neuropsychology and Molecular Genetics and Metabolism.

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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