Forbes D. Porter

12.8k citations

213 papers · 8.6k indexed · h-index 51

Physiology top 0.2%
- Lysosomal Storage Disorders Research 109
- Calcium signaling and nucleotide metabolism 20
Physiology top 0.5%
- Lysosomal Storage Disorders Research 109
- Calcium signaling and nucleotide metabolism 20
Developmental Neuroscience top 1%
Molecular Biology top 1%
- Peroxisome Proliferator-Activated Receptors 35
Cell Biology top 1%
Surgery
- Cholesterol and Lipid Metabolism 59
Organic Chemistry
- Carbohydrate Chemistry and Synthesis 31
Hematology
- Autoimmune and Inflammatory Disorders Research 22
Epidemiology
- Cytomegalovirus and herpesvirus research 18
Rheumatology
- Glycogen Storage Diseases and Myoclonus 17

Co-authors: Christopher A. Wassif Gail E. Herman Heiner Westphal Nicole M. Yanjanin Frances M. Platt Simona Bianconi Christopher A. Walsh Edwin S. Monuki
Cited by: Physiology Developmental Neuroscience
Journals: Nature (2 papers)Proceedings of the National Academy of Sciences (2 papers)Journal of Biological Chemistry (3 papers)
Partner nations: United States United Kingdom Canada

In The Last Decade

Forbes D. Porter

203 papers receiving 8.5k citations

Peers

Countries citing papers authored by Forbes D. Porter

Since Specialization

Citations

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

Fields of papers citing papers by Forbes D. Porter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Forbes D. Porter. 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 Forbes D. Porter. The network helps show where Forbes D. Porter may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Forbes D. Porter, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Forbes D. Porter Line = papers co-authored together Forbes D. Porter links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Prevalence of Neutralizing Antibodies to AAV2 and AAV9 in Individuals with Niemann-Pick Disease, Type C1 Human Gene Therapy ·Avani V. Mylvara,Cristin Davidson,Derek Alexander,Charles P. Venditti,Forbes D. Porter	2025	0
2	Cerebrospinal Fluid and Serum Neuron‐Specific Enolase in Niemann‐Pick Disease Type C1 American Journal of Medical Genetics Part A ·Cameron Padilla,Derek Alexander,Desiree A. Labor,Orsolya K. Albert,Kenneth E. Robbins,Elizabeth Berry‐Kravis,Forbes D. Porter	2024	0
3	Elevated cerebrospinal fluid glial fibrillary acidic protein levels in Smith-Lemli-Opitz syndrome Molecular Genetics and Metabolism ·Rachel Luke,Niamh X. Cawley,Samar Rahhal,Aishwarya Selvaraman,Audrey Thurm,Christopher A. Wassif,Forbes D. Porter	2024	1
4	Assessing Postnatal Mortality in Smith–Lemli–Opitz Syndrome American Journal of Medical Genetics Part A ·Aishwarya Selvaraman,Samar Rahhal,Simona Bianconi,Tristan Furnary,Forbes D. Porter	2024	1
5	Brain proton MR spectroscopy measurements in CLN3 disease Molecular Genetics and Metabolism ·An Dang,Eva H. Baker,Cristan Farmer,Ariane Soldatos,Audrey Thurm,Forbes D. Porter	2023	1
6	Elevated oxysterol and N‐palmitoyl‐O‐phosphocholineserine levels in congenital disorders of glycosylation Journal of Inherited Metabolic Disease ·An Dang,Irene J. Chang,Xutian Jiang,Lynne A. Wolfe,Bobby G. Ng,Christina Lam,Rhonda E. Schnur,Katrina Allis,Hana Hansíková,Nina Ondrušková,Shawn O’Connor,Amarilis Sanchez‐Valle,Arve Vøllo,Raymond Wang,Zoe Wolfenson,John Perreault,Daniel S. Ory,Hudson H. Freeze,J. Lawrence Merritt,Forbes D. Porter	2023	4
7	Auditory phenotype of Smith–Lemli–Opitz syndrome American Journal of Medical Genetics Part A ·Christopher Zalewski,Sarah Sydlowski,Kelly King,Simona Bianconi,An Dang,Forbes D. Porter,Carmen C. Brewer	2021	4
8	Scoping review of COVID-19-related systematic reviews and meta-analyses: can we really have confidence in their results? Postgraduate Medical Journal ·Rachel Wurth,Michelle Hajdenberg,Francisco J. Barrera,Skand Shekhar,Caroline E. Copacino,Pablo J. Moreno‐Peña,Omar A M Gharib,Forbes D. Porter,Swapnil Hiremath,Janet E. Hall,Ernesto L. Schiffrin,Graeme Eisenhofer,Stefan R. Bornstein,Juan P. Brito,José Gerardo González‐González,Constantine A. Stratakis,René Rodríguez‐Gutiérrez,Fady Hannah‐Shmouni	2021	7
9	Disruption of Dhcr7 and Insig1/2 in cholesterol metabolism causes defects in bone formation and homeostasis through primary cilium formation Bone Research ·Akiko Suzuki,Kenichi Ogata,Hiroki Yoshioka,Junbo Shim,Christopher A. Wassif,Forbes D. Porter,Junichi Iwata	2020	34
10	Prevalence of Diabetes and Hypertension and Their Associated Risks for Poor Outcomes in Covid-19 Patients Journal of the Endocrine Society ·Francisco J. Barrera,Skand Shekhar,Rachel Wurth,Pablo J. Moreno‐Peña,Oscar J. Ponce,Michelle Hajdenberg,Neri Alejandro Álvarez‐Villalobos,Janet E. Hall,Ernesto L. Schiffrin,Graeme Eisenhofer,Forbes D. Porter,Juan P. Brito,Stefan R. Bornstein,Constantine A. Stratakis,José Gerardo González‐González,René Rodríguez‐Gutiérrez,Fady Hannah‐Shmouni	2020	53
11	Endocrine Conditions and COVID-19 Hormone and Metabolic Research ·Skand Shekhar,Rachel Wurth,Crystal Kamilaris,Graeme Eisenhofer,Francisco J. Barrera,Michelle Hajdenberg,Joselyne Tonleu,Janet E. Hall,Ernesto L. Schiffrin,Forbes D. Porter,Constantine A. Stratakis,Fady Hannah‐Shmouni	2020	32
12	Abnormal LAMP1 glycosylation may play a role in Niemann-Pick disease, type C pathology PLoS ONE ·Niamh X. Cawley,Caitlin Sojka,Antony Cougnoux,A. Lyons,Elena‐Raluca Nicoli,Christopher A. Wassif,Forbes D. Porter	2020	24
13	Mechanistic convergence and shared therapeutic targets in Niemann‐Pick disease Journal of Inherited Metabolic Disease ·Alexandria Colaço,Ecem Kaya,Elias Adriaenssens,Lianne C. Davis,Stefania Zampieri,María E. Fernández‐Suárez,Chong Yew Tan,Patrick Deegan,Forbes D. Porter,(unknown),Bruno Bembi,Andrea Dardis,Frances M. Platt	2019	15
14	High incidence of unrecognized visceral/neurological late-onset Niemann-Pick disease, type C1, predicted by analysis of massively parallel sequencing data sets Genetics in Medicine ·Christopher A. Wassif,Joanna Cross,James Iben,Luis Sánchez‐Pulido,Antony Cougnoux,Frances M. Platt,Daniel Ory,Chris P. Ponting,Joan E. Bailey‐Wilson,Leslie G. Biesecker,Forbes D. Porter	2015	156
15	Brain magnetic resonance imaging findings in smith–lemli–opitz syndrome American Journal of Medical Genetics Part A ·Ryan W.Y. Lee,Sandra K. Conley,Andrea Gropman,Forbes D. Porter,Eva H. Baker	2013	35
16	Altered vitamin E status in Niemann-Pick type C disease Journal of Lipid Research ·Lynn Ulatowski,Robert S. Parker,Cristin Davidson,Nicole M. Yanjanin,Thomas J. Kelley,Deborah A. Corey,Jeffrey Atkinson,Forbes D. Porter,Hiroyuki Arai,Steven U. Walkley,Danny Manor	2011	33
17	Analysis of short‐term behavioral effects of dietary cholesterol supplementation in Smith–Lemli–Opitz syndrome American Journal of Medical Genetics Part A ·Elaine Tierney,Sandra K. Conley,H. Goodwin,Forbes D. Porter	2009	46
18	Malformation syndromes due to inborn errors of cholesterol synthesis Journal of Clinical Investigation ·Forbes D. Porter	2002	4
19	Malformation syndromes due to inborn errors of cholesterol synthesis Journal of Clinical Investigation ·Forbes D. Porter	2002	77
20	A Simple PCR-Based Assay Allows Detection of a Common Mutation, IVS8-1G→C, in DHCR7 in Smith-Lemli-Opitz Syndrome Genetic Testing ·K.P. Battaile,Cheryl L. Maslen,Christopher A. Wassif,Patrycja A. Krakowiak,Forbes D. Porter,Robert D. Steiner	1999	10

About Forbes D. Porter

Forbes D. Porter is a scholar working on Physiology, Physiology and Biochemistry, having authored 213 papers that have together received 8.6k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (109 papers), Cholesterol and Lipid Metabolism (59 papers), Peroxisome Proliferator-Activated Receptors (35 papers), Carbohydrate Chemistry and Synthesis (31 papers), Autoimmune and Inflammatory Disorders Research (22 papers), Calcium signaling and nucleotide metabolism (20 papers), Cytomegalovirus and herpesvirus research (18 papers) and Glycogen Storage Diseases and Myoclonus (17 papers). The work is most often cited by research in Physiology (635 citations), Physiology (2.5k citations) and Developmental Neuroscience (324 citations). Forbes D. Porter has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Christopher A. Wassif, Gail E. Herman, Heiner Westphal, Nicole M. Yanjanin, Frances M. Platt, Simona Bianconi, Christopher A. Walsh, Edwin S. Monuki, Rohini Sidhu and Daniel S. Ory. Their work appears in journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

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