Gerardo Del Valle

576 citations

12 papers · 334 indexed · h-index 8

Co-authors: Patricia Cuenca Fernando Morales Luis Sanchez‐Ramos Francisco L. Gaudier Darren G. Monckton Tetsuo Ashizawa Andrew M. Kaunitz Isaac Delke
Topics: Genetic Neurodegenerative Diseases (7 papers)Hereditary Neurological Disorders (4 papers)Ion channel regulation and function (3 papers)
Cited by: Cellular and Molecular Neuroscience Obstetrics and Gynecology Neurology
Journals: The American Journal of Human Genetics Human Molecular Genetics American Journal of Obstetrics and Gynecology
Partner nations: Costa Rica Germany United States

In The Last Decade

Gerardo Del Valle

12 papers receiving 326 citations

Peers

Countries citing papers authored by Gerardo Del Valle

Since Specialization

Citations

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

Fields of papers citing papers by Gerardo Del Valle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gerardo Del Valle. 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 Gerardo Del Valle. The network helps show where Gerardo Del Valle may publish in the future.

Co-authorship network of co-authors of Gerardo Del Valle

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

All Works

Sort: Min cites: Since: Top N: Style:

12 of 12 papers shown

#	Work	Indexed citations
1	Functional and Structural Characterization of ClC-1 and Nav1.4 Channels Resulting from CLCN1 and SCN4A Mutations Identified Alone and Coexisting in Myotonic Patients 2021 ·Cells ·(unknown),Raffaella Barbieri,(unknown),(unknown),(unknown),Adarli Romero,Gerardo Del Valle,(unknown),Sara Bertelli,Michael Pusch,Fernando Morales	2
2	Identification and Functional Characterization ofCLCN1Mutations Found in Nondystrophic Myotonia Patients 2015 ·Human Mutation ·(unknown),Michele Fiore,(unknown),Patricia Cuenca,Gerardo Del Valle,Laura Lagostena,Héctor Gaitán‐Peñas,Raúl Estévez,Michael Pusch,Fernando Morales	20
3	Parental age effects, but no evidence for an intrauterine effect in the transmission of myotonic dystrophy type 1 2014 ·European Journal of Human Genetics ·Fernando Morales,(unknown),Patricia Cuenca,Domingo Campos,(unknown),Gerardo Del Valle,(unknown),(unknown),Darren G. Monckton	20
4	Somatic instability of the expanded CTG triplet repeat in myotonic dystrophy type 1 is a heritable quantitative trait and modifier of disease severity 2012 ·Human Molecular Genetics ·Fernando Morales,Jillian M. Couto,Catherine F. Higham,Grant Hogg,Patricia Cuenca,(unknown),Richard H. Wilson,Berit Adam,Gerardo Del Valle,(unknown),(unknown),Tetsuo Ashizawa,Alison Wilcox,D.E. Wilcox,Darren G. Monckton	128
5	Late onset autosomal dominant Charcot–Marie–Tooth 2 neuropathy in a Costa Rican family 2008 ·Neurological Research ·(unknown),Martin Berghoff,Alejandro Leal,Bernal Morera-Brenes,(unknown),Ramiro Barrantes,Bernd Rautenstrauß,Gerardo Del Valle,Dieter Heuß	3
6	Gene symbol: CLCN1. Disease: Myotonia congenita. 2008 ·PubMed ·Fernando Morales,Patricia Cuenca,Gerardo Del Valle,(unknown),(unknown),(unknown),Keith Johnson,Xi Lin,Tetsuo Ashizawa	1
7	Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenita (Becker disease) carrying a new mutation in the CLCN1 gene 2006 ·Revista de Biología Tropical ·Fernando Morales,Patricia Cuenca,Gerardo Del Valle,(unknown),(unknown),(unknown),Keith Johnson,Xi Lin,Tetsuo Ashizawa	8
8	Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3 2004 ·Neuromuscular Disorders ·(unknown),Martin Berghoff,Alejandro Leal,Bernal Morera-Brenes,Ramiro Barrantes,André Reis,B. Neundörfer,Bernd Rautenstrauß,Gerardo Del Valle,Dieter Heuß	14
9	Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero ( MPZ , P0 ) gene causes different phenotypes in homozygous and heterozygous carriers within one family 2003 ·Neurogenetics ·Alejandro Leal,(unknown),Martin Berghoff,Gerardo Del Valle,Carlos Contreras,(unknown),(unknown),Ramiro Barrantes,(unknown),(unknown),André Reis,Bernd Rautenstrauß,Dieter Heuß	14
10	A Second Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 19q13.3 2001 ·The American Journal of Human Genetics ·Alejandro Leal,Bernal Morera-Brenes,Gerardo Del Valle,Dieter Heuß,(unknown),Martin Berghoff,(unknown),(unknown),María Méndez,Hans Christian Hennies,B. Neundörfer,Ramiro Barrantes,André Reis,Bernd Rautenstrauß	49
11	Randomized trial of two doses of the prostaglandin E1 analog misoprostol for labor induction 1997 ·American Journal of Obstetrics and Gynecology ·(unknown),Luis Sanchez‐Ramos,(unknown),Gerardo Del Valle,Francisco L. Gaudier,Isaac Delke,Andrew M. Kaunitz	72
12	Interpretation of the TDx-FLM Fluorescence Polarization Assay in Pregnancies Complicated by Diabetes Mellitus 1997 ·American Journal of Perinatology ·Gerardo Del Valle,C. David Adair,(unknown),Francisco L. Gaudier,Luis Sanchez‐Ramos,(unknown)	3

About Gerardo Del Valle

Gerardo Del Valle is a scholar working on Cellular and Molecular Neuroscience, Obstetrics and Gynecology and Neurology, having authored 12 papers that have together received 334 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (7 papers), Hereditary Neurological Disorders (4 papers) and Ion channel regulation and function (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (223 citations), Obstetrics and Gynecology (66 citations) and Neurology (71 citations). Gerardo Del Valle has collaborated with scholars based in Costa Rica, Germany and United States. Frequent co-authors include Patricia Cuenca, Fernando Morales, Luis Sanchez‐Ramos, Francisco L. Gaudier, Darren G. Monckton, Tetsuo Ashizawa, Andrew M. Kaunitz, Isaac Delke, Richard H. Wilson and Grant Hogg. Their work appears in journals such as The American Journal of Human Genetics, Human Molecular Genetics and American Journal of Obstetrics and Gynecology.

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.

Explore authors with similar magnitude of impact