Heidi Fodstad

1.0k total citations
26 papers, 673 citations indexed

About

Heidi Fodstad is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Heidi Fodstad has authored 26 papers receiving a total of 673 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 11 papers in Cardiology and Cardiovascular Medicine and 4 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Heidi Fodstad's work include Ion channel regulation and function (12 papers), Cardiac electrophysiology and arrhythmias (10 papers) and Receptor Mechanisms and Signaling (5 papers). Heidi Fodstad is often cited by papers focused on Ion channel regulation and function (12 papers), Cardiac electrophysiology and arrhythmias (10 papers) and Receptor Mechanisms and Signaling (5 papers). Heidi Fodstad collaborates with scholars based in Finland, Switzerland and France. Heidi Fodstad's co-authors include Kimmo Kontula, Heikki Swan, Lauri Toivonen, Kirsi Piippo, Matti Viitasalo, Päivi Laitinen, Päivi J. Laitinen-Forsblom, Tuula Hannila‐Handelberg, Timo P. Hiltunen and Kristian Paavonen and has published in prestigious journals such as Journal of the American College of Cardiology, Analytical Biochemistry and Kidney International.

In The Last Decade

Heidi Fodstad

24 papers receiving 659 citations

Peers

Countries citing papers authored by Heidi Fodstad

Since Specialization

Citations

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

Fields of papers citing papers by Heidi Fodstad

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heidi Fodstad

This figure shows the co-authorship network connecting the top 25 collaborators of Heidi Fodstad. A scholar is included among the top collaborators of Heidi Fodstad 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 Heidi Fodstad. Heidi Fodstad 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	Mosaic RASopathies concept: different skin lesions, same systemic manifestations? 2024 ·Journal of Medical Genetics ·Marie‐Anne Morren, Heidi Fodstad, Hilde Brems, Nicola Bedoni, Emmanuella Guenova, (unknown), Kanetee Busiah, Fabienne Giuliano, Michel Gilliet, Isis Atallah	3
2	Homozygous GLI3 variants observed in three unrelated patients presenting with syndromic polydactyly 2021 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), Sandra Whalen, (unknown), Sophie Kaltenbach, Andrea Superti‐Furga, Michel Vekemans, Heidi Fodstad, Fabienne Giuliano, Tania Attié‐Bitach	0
3	Case Report: A Rare Truncating Variant of the CFHR5 Gene in IgA Nephropathy 2021 ·Frontiers in Genetics ·Gabriella Guzzo, Salima Sadallah, Heidi Fodstad, Jean-Pierre Venetz, Samuel Rotman, Daniel Teta, Thierry Gauthier, Giuseppe Pantaleo, Andrea Superti‐Furga, Manuel Pascual	3
4	Clinical and Genetic Findings in a Series of Eight Families with Arthrogryposis 2021 ·Genes ·Marzia Pollazzon, Stefano Giuseppe Caraffi, Silvia Faccioli, Simonetta Rosato, Heidi Fodstad, Belinda Campos‐Xavier, (unknown), Giuseppina Comitini, Daniele Frattini, Teresa Grimaldi Capitello, (unknown), Davide Martorana, Antonio Percesepe, (unknown), Carlo Fusco, Giancarlo Gargano, Andrea Superti‐Furga, Livia Garavelli	10
5	Childhood neurodegeneration associated with a specific UBTF variant: a new case report and review of the literature 2020 ·BMC Neurology ·(unknown), Mathieu Quinodoz, Marie‐Claude Addor, Béryl Royer‐Bertrand, Heidi Fodstad, Carlo Rivolta, Claudia Poloni, Andrea Superti‐Furga, Eliane Roulet‐Perez, Sébastien Lebon	13
6	Chronic potassium depletion increases adrenal progesterone production that is necessary for efficient renal retention of potassium 2011 ·Kidney International ·(unknown), Aurélie Edwards, (unknown), Anie Azroyan, Heidi Fodstad, Pierre Meneton, Alain Doucet, May Bloch-Faure, Gilles Crambert	38
7	Common genetic variation of β1- and β2-adrenergic receptor and response to four classes of antihypertensive treatment 2010 ·Pharmacogenetics and Genomics ·(unknown), Kati Donner, Tuula Hannila‐Handelberg, Heidi Fodstad, Kimmo Kontula, Timo P. Hiltunen	30
8	Effects of mineralocorticoid and K⁺concentration on K⁺secretion and ROMK channel expression in a mouse cortical collecting duct cell line 2009 ·American Journal of Physiology-Renal Physiology ·Heidi Fodstad, Elena González Rodríguez, (unknown), H. P. Gaeggeler, Barbara Guisan, Bernard C. Rossier, Jean‐Daniel Horisberger	23
9	Renin–Angiotensin System and α-Adducin Gene Polymorphisms and Their Relation to Responses to Antihypertensive Drugs: Results From the GENRES Study 2008 ·American Journal of Hypertension ·(unknown), Tuula Hannila‐Handelberg, Heidi Fodstad, Kati Donner, Kimmo Kontula, Timo P. Hiltunen	26
10	Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients 2006 ·Annals of Medicine ·Heidi Fodstad, Saı̈d Bendahhou, Jean‐Sébastien Rougier, Päivi J. Laitinen-Forsblom, Jacques Barhanin, Hugues Abriel, Laurent Schild, Kimmo Kontula, Heikki Swan	32
11	β1-Adrenergic receptor polymorphisms, QTc interval and occurrence of symptoms in type 1 of long QT syndrome 2006 ·International Journal of Cardiology ·Kristian Paavonen, Heikki Swan, Kirsi Piippo, Päivi Laitinen, Heidi Fodstad, Seppo Sarna, Lauri Toivonen, Kimmo Kontula, Matti Viitasalo	8
12	Common variants of the beta and gamma subunits of the epithelial sodium channel and their relation to plasma renin and aldosterone levels in essential hypertension 2005 ·BMC Medical Genetics ·Tuula Hannila‐Handelberg, Kimmo Kontula, Ilkka Tikkanen, Tuula Tikkanen, Frej Fyhrquist, Kristian Helin, Heidi Fodstad, Kirsi Piippo, Helena E. Miettinen, Jarmo Virtamo, Tom Krusius, Seppo Sarna, Ivan Gautschi, Laurent Schild, Timo P. Hiltunen	53
13	Ratio of Late to Early T-Wave Peak Amplitude in 24-h Electrocardiographic Recordings as Indicator of Symptom History in Patients With Long-QT Syndrome Types 1 and 2 2005 ·Journal of the American College of Cardiology ·Matti Viitasalo, Lasse Oikarinen, Heikki Swan, Kathryn A. Glatter, Heikki Väänänen, Heidi Fodstad, Nipavan Chiamvimonvat, Kimmo Kontula, Lauri Toivonen, Melvin M. Scheinman	15
14	Loss-of-function mutations of the K+ channel gene KCNJ2 constitute a rare cause of long QT syndrome 2004 ·Journal of Molecular and Cellular Cardiology ·Heidi Fodstad	30
15	Four potassium channel mutations account for 73% of the genetic spectrum underlying long‐QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland 2004 ·Annals of Medicine ·Heidi Fodstad, Heikki Swan, Päivi Laitinen, Kirsi Piippo, Kristian Paavonen, Matti Viitasalo, Lauri Toivonen, Kimmo Kontula	80
16	Molecular screening of selected long QT syndrome (LQTS) mutations in 165 consecutive bodies found in water 2003 ·International Journal of Legal Medicine ·Philippe Lunetta, Antti Levo, (unknown), Heidi Fodstad, Kimmo Kontula, Antti Sajantila	17
17	Multiplex genotyping of the human β2-adrenergic receptor gene using solid-phase capturable dideoxynucleotides and mass spectrometry 2003 ·Analytical Biochemistry ·Sobin Kim, Shundi Shi, Tomás Bonome, (unknown), John R. Edwards, Heidi Fodstad, James J. Russo, Jingyue Ju	14
18	association between HERG K897T polymorphism and QT interval in middle-aged finnish women 2002 ·Journal of the American College of Cardiology ·E M Pietilä, Heidi Fodstad, (unknown), (unknown), Heikki Swan, Markku J. Savolainen, Y. Antero Kesäniemi, Kimmo Kontula, Heikki V. Huikuri	78
19	Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects 2000 ·Human Mutation ·Päivi Laitinen, Heidi Fodstad, Kirsi Piippo, Heikki Swan, Lauri Toivonen, Matti Viitasalo, Jaakko Kaprio, Kimmo Kontula	59
20	Genetic Markers in Patients with Intracranial Aneurysms 1987 ·Human Heredity ·(unknown), G. Beckman, L. Beckman, B. Cedergren, Heidi Fodstad, (unknown)	25

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