Esperanza Font–Montgomery

919 citations

14 papers · 334 indexed · h-index 9

Co-authors: William A. Gahl Joy Bryant Meral Gunay‐Aygun M. Tuchman Theo Heller Peter L. Choyke Kailash Daryanani Parvathi Mohan
Topics: Genetic and Kidney Cyst Diseases (4 papers)Renal and related cancers (4 papers)Lysosomal Storage Disorders Research (4 papers)
Cited by: Genetics Clinical Biochemistry Pediatrics, Perinatology and Child Health
Journals: The Lancet Journal of Pediatric Gastroenterology and Nutrition Molecular Genetics and Metabolism
Partner nations: United States Germany Australia

In The Last Decade

Esperanza Font–Montgomery

14 papers receiving 329 citations

Peers

Countries citing papers authored by Esperanza Font–Montgomery

Since Specialization

Citations

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

Fields of papers citing papers by Esperanza Font–Montgomery

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Esperanza Font–Montgomery. 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 Esperanza Font–Montgomery. The network helps show where Esperanza Font–Montgomery may publish in the future.

Co-authorship network of co-authors of Esperanza Font–Montgomery

This figure shows the co-authorship network connecting the top 25 collaborators of Esperanza Font–Montgomery. A scholar is included among the top collaborators of Esperanza Font–Montgomery 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 Esperanza Font–Montgomery. Esperanza Font–Montgomery is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Safety and efficacy of migalastat in adolescent patients with Fabry disease: Results from ASPIRE, a phase 3b, open-label, single-arm, 12-month clinical trial, and its open-label extension 2025 ·Molecular Genetics and Metabolism ·Uma Ramaswami,Esperanza Font–Montgomery,Özlem Göker-Alpan,Damara Ortiz,Amarilis Sanchez‐Valle,Chester B. Whitley,William R. Wilcox,Hai Jiang,Lee Ann Lawson,(unknown),Haichen Yang,Robert J. Hopkin	3
2	The role of biomarkers for the follow up of infants with positive newborn screening results for Fabry disease 2021 ·Molecular Genetics and Metabolism ·(unknown),(unknown),Amy White,Dawn Peck,(unknown),(unknown),(unknown),Jennifer Gannon,Bryce A. Heese,Esperanza Font–Montgomery,(unknown),(unknown),(unknown),Dimitar Gavrilov,Silvia Tortorelli,Devin Oglesbee,Piero Rinaldo,Dietrich Matern,Kimiyo Raymond	2
3	Prospective evaluation of kidney and liver disease in autosomal recessive polycystic kidney disease-congenital hepatic fibrosis 2020 ·Molecular Genetics and Metabolism ·(unknown),Esperanza Font–Montgomery,(unknown),Joy Bryant,(unknown),Peter L. Choyke,Barış Türkbey,Theo Heller,William A. Gahl,Meral Gunay‐Aygun	11
4	Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra‐rare disease 2020 ·Journal of Inherited Metabolic Disease ·Laura Adang,Lars Schlotawa,Samuel Groeschel,Christiane Kehrer,K. Harzer,Orna Staretz‐Chacham,(unknown),Ida Vanessa Döederlein Schwartz,Jutta Gärtner,Mauricio De Castro,(unknown),Esperanza Font–Montgomery,Thomas Dierks,Karthikeyan Radhakrishnan,Rebecca C. Ahrens‐Nicklas	18
5	Response to letter to the editor: Why does Leigh syndrome responds to immunotherapy? 2016 ·Molecular Genetics and Metabolism Reports ·(unknown),Raghav Govindarajan,Dawn Peck,Esperanza Font–Montgomery	1
6	Response to immunotherapy in a patient with adult onset Leigh syndrome and T9176C mtDNA mutation 2016 ·Molecular Genetics and Metabolism Reports ·(unknown),Raghav Govindarajan,Dawn Peck,Esperanza Font–Montgomery	12
7	Newborn screening for Fabry disease: Is the A143T allele a pathogenic mutation or a pseudodeficiency allele? 2015 ·Molecular Genetics and Metabolism ·Andrea M. Atherton,Dana Doheny,Dawn Peck,Katherine Christensen,Kayla Smith,Linda Manwaring,(unknown),Richard E. Hillman,Esperanza Font–Montgomery,Marwan Shinawi,Dorothy K. Grange,Robert J. Desnick,Bryce A. Heese	1
8	Efficacy and safety of cyclic pyranopterin monophosphate substitution in severe molybdenum cofactor deficiency type A: a prospective cohort study 2015 ·The Lancet ·Bernd Schwahn,Francjan J. van Spronsen,Abdel Ali Belaidi,(unknown),John Christodoulou,Terry G. J. Derks,Julia B. Hennermann,Elisabeth Jameson,Kai König,Tracy L. McGregor,Esperanza Font–Montgomery,José Angel Santamaria‐Araujo,Saikat Santra,(unknown),Anne Vierzig,Evangeline Wassmer,(unknown),Flora Y. Wong,Alex Veldman,Günter Schwarz	99
9	The first two years of full population pilot newborn screening for lysosomal disorders: The Missouri experience 2015 ·Molecular Genetics and Metabolism ·Andrea M. Atherton,Dawn Peck,Katherine Christensen,Kayla Smith,Linda Manwaring,Patrick V. Hopkins,(unknown),(unknown),Esperanza Font–Montgomery,Richard E. Hillman,Stephen R. Braddock,Marwan Shinawi,Dorothy K. Grange,Bryce A. Heese	1
10	Congenital Hepatic Fibrosis and Portal Hypertension in Autosomal Dominant Polycystic Kidney Disease 2011 ·Journal of Pediatric Gastroenterology and Nutrition ·Kevin O’Brien,Esperanza Font–Montgomery,(unknown),Joy Bryant,Katie Piwnica–Worms,Hailey Edwards,Lauren C. Riney,(unknown),Kailash Daryanani,Peter L. Choyke,Parvathi Mohan,Theo Heller,William A. Gahl,Meral Gunay‐Aygun	19
11	PKHD1 sequence variations in 78 children and adults with autosomal recessive polycystic kidney disease and congenital hepatic fibrosis 2009 ·Molecular Genetics and Metabolism ·Meral Gunay‐Aygun,M. Tuchman,Esperanza Font–Montgomery,(unknown),Hailey Edwards,(unknown),(unknown),Shira G. Ziegler,Katie Piwnica–Worms,Joy Bryant,Isa Bernardini,Roxanne Fischer,Marjan Huizing,Lisa M. Guay‐Woodford,William A. Gahl	66
12	Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF) 2008 ·Pediatric Radiology ·Barış Türkbey,İclal Ocak,Kailash Daryanani,Esperanza Font–Montgomery,(unknown),Joy Bryant,M. Tuchman,Parvathi Mohan,Theo Heller,William A. Gahl,Peter L. Choyke,Meral Gunay‐Aygun	69
13	Clinical outcome and follow‐up of the first reported case of Russell‐Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic trisomy 7 2005 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Esperanza Font–Montgomery,(unknown),David D. Weaver,Gail H. Vance,Soma Das,Virginia C. Thurston	22
14	Clinical and cytogenetic manifestations of subtelomeric aberrations: Report of six cases 2004 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Esperanza Font–Montgomery,David D. Weaver,Laurence E. Walsh,Celanie K. Christensen,Virginia C. Thurston	10

About Esperanza Font–Montgomery

Esperanza Font–Montgomery is a scholar working on Clinical Biochemistry, Genetics and Physiology, having authored 14 papers that have together received 334 indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (4 papers), Renal and related cancers (4 papers) and Lysosomal Storage Disorders Research (4 papers). The work is most often cited by research in Genetics (193 citations), Clinical Biochemistry (37 citations) and Pediatrics, Perinatology and Child Health (59 citations). Esperanza Font–Montgomery has collaborated with scholars based in United States, Germany and Australia. Frequent co-authors include William A. Gahl, Joy Bryant, Meral Gunay‐Aygun, M. Tuchman, Theo Heller, Peter L. Choyke, Kailash Daryanani, Parvathi Mohan, Barış Türkbey and Hailey Edwards. Their work appears in journals such as The Lancet, Journal of Pediatric Gastroenterology and Nutrition 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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