Pia Höglund

3.6k citations

27 papers · 1.4k indexed · h-index 21

Molecular Biology top 10%
Pulmonary and Respiratory Medicine top 10%
Surgery top 10%
Genetics top 10%
Nutrition and Dietetics top 10%

Co-authors: Juha Kere Christer Holmberg Siru Haila Albert de la Chapelle Siru Mäkelä Jerzy Socha Kristiina Airola Ulpu Saarialho‐Kere
Topics: Ion Transport and Channel Regulation (14 papers)Helicobacter pylori-related gastroenterology studies (11 papers)Potassium and Related Disorders (9 papers)
Cited by: Sensory Systems Gastroenterology Molecular Biology
Journals: Nature Genetics Oncogene Scientific Reports
Partner nations: Finland Sweden United States

In The Last Decade

Pia Höglund

27 papers receiving 1.4k citations

Peers

Countries citing papers authored by Pia Höglund

Since Specialization

Citations

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

Fields of papers citing papers by Pia Höglund

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pia Höglund

This figure shows the co-authorship network connecting the top 25 collaborators of Pia Höglund. A scholar is included among the top collaborators of Pia Höglund 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 Pia Höglund. Pia Höglund 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	A missense mutation in SLC26A3 is associated with human male subfertility and impaired activation of CFTR 2017 ·Scientific Reports ·Satu Wedenoja,(unknown),(unknown),(unknown),Outi Elomaa,Jorma Toppari,Pia Höglund,Kristiina Aittomäki,Christer Holmberg,Outi Hovatta,Juha S. Tapanainen,Ehud Ohana,Juha Kere	21
2	Follow‐up of a child with congenital chloride diarrhoea caused by a novel mutation 2012 ·Acta Paediatrica ·(unknown),Satu Wedenoja,Pia Höglund,(unknown),Klaus‐Peter Zimmer,Matthias Heckmann	2
3	Update on SLC26A3 mutations in congenital chloride diarrhea 2011 ·Human Mutation ·Satu Wedenoja,(unknown),Pia Höglund,Siru Mäkelä,Christer Holmberg,Juha Kere	88
4	Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD) 2009 ·BMC Gastroenterology ·(unknown),(unknown),Taina Routi,(unknown),Carlo Catassi,Pia Höglund,Erkki Savilahti,Irma Järvelä	30
5	Cl− Is Required for HCO3− Entry Necessary for Sperm Capacitation in Guinea Pig: Involvement of a Cl−/HCO3− Exchanger (SLC26A3) and CFTR1 2008 ·Biology of Reproduction ·Wen Ying Chen,Wenming Xu,(unknown),Ya Ni,Yu Yuan,(unknown),(unknown),Lai Ling Tsang,Yiu Wa Chung,Pia Höglund,Hsiao Chang Chan,Qi Shi	70
6	The impact of sodium chloride and volume depletion in the chronic kidney disease of congenital chloride diarrhea 2008 ·Kidney International ·Satu Wedenoja,Timo Örmälä,Ulla Berg,(unknown),Hannu Jalanko,Riitta Karikoski,Juha Kere,Christer Holmberg,Pia Höglund	26
7	Expression of ion transport-associated proteins in human efferent and epididymal ducts 2007 ·Reproduction ·Minna Kujala,(unknown),Jukka Tienari,Kari Kaunisto,Johanna Hästbacka,Christer Holmberg,Juha Kere,Pia Höglund	60
8	Disruption of the SLC26A3-mediated anion transport is associated with male subfertility 2006 ·Fertility and Sterility ·Pia Höglund,(unknown),Minna Kujala,Aila Tiitinen,Leo Dunkel,Christer Holmberg	36
9	Phenotypic consequences of genetic variation at hemizygous alleles: Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency 2005 ·Genetics in Medicine ·Naohiro Kurotaki,Joseph Shen,(unknown),Tatsuro Kondoh,Remco Visser,Takao Ozaki,Junji Nishimoto,Takashi Shiihara,Kimiaki Uetake,Yoshio Makita,Naoki Harada,Salmo Raskin,Chester Brown,Pia Höglund,Nobuhiko Okamoto,James R. Lupski	33
10	Interstitial 1q25.3‐q31.3 deletion in a boy with mild manifestations 2003 ·American Journal of Medical Genetics Part A ·Pia Höglund,(unknown),Eino Marttinen,Tiina Alitalo	10
11	SLC26A3 mutations in congenital chloride diarrhea 2002 ·Human Mutation ·Siru Mäkelä,Juha Kere,Christer Holmberg,Pia Höglund	114
12	Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea 2001 ·Human Mutation ·Pia Höglund,Markus Sormaala,Siru Haila,Jerzy Socha,(unknown),Wolfram Scheurlen,M. Sinaasappel,Hugo de Jonge,Christer Holmberg,Hideto Yoshikawa,Juha Kere	26
13	Maternal and Paternal Chromosomes 7 Show Differential Methylation of Many Genes in Lymphoblast DNA 2001 ·Genomics ·Katariina Hannula‐Jouppi,Marita Lipsanen‐Nyman,Stephen W. Scherer,Christer Holmberg,Pia Höglund,Juha Kere	23
14	The congenital chloride diarrhea gene is expressed in seminal vesicle, sweat gland, inflammatory colon epithelium, and in some dysplastic colon cells 2000 ·Histochemistry and Cell Biology ·Siru Haila,Ulpu Saarialho‐Kere,Marja-Liisa Karjalainen-Lindsberg,Hannes Lohi,Kristiina Airola,Christer Holmberg,(unknown),Juha Kere,Pia Höglund	53
15	Molecular characterization of deletion at 11q22.1‐23.3 in mantle cell lymphoma 1999 ·British Journal of Haematology ·Outi Monni,Ying Zhu,Kaarle Franssila,(unknown),Pia Höglund,Erkki Elonen,Heikki Joensuu,Sakari Knuutila	37
16	Intestinal cancer in patients with a germline mutation in the down-regulated in adenoma (DRA) gene 1998 ·Oncogene ·Akseli Hemminki,Pia Höglund,Eero Pukkala,Reijo Salovaara,Heikki Järvinen,Reijo Norio,Lauri A. Aaltonen	17
17	Genomic structure of the human congenital chloride diarrhea (CLD) gene 1998 ·Gene ·Siru Haila,Pia Höglund,Stephen W. Scherer,Jeffrey R. Lee,Paula Kristo,Beth Coyle,Richard C. Trembath,Christer Holmberg,Albert de la Chapelle,Juha Kere	24
18	Genetic Background of Congenital Chloride Diarrhea in High-Incidence Populations: Finland, Poland, and Saudi Arabia and Kuwait 1998 ·The American Journal of Human Genetics ·Pia Höglund,Mari Auranen,Jerzy Socha,(unknown),Hisham M. Nazer,(unknown),(unknown),(unknown),(unknown),Albert de la Chapelle,Juha Kere	60
19	Mutations of the Down–regulated in adenoma (DRA) gene cause congenital chloride diarrhoea 1996 ·Nature Genetics ·Pia Höglund,Siru Haila,Jerzy Socha,L Tomaszewski,Ulpu Saarialho‐Kere,Marja‐Liisa Karjalainen‐Lindsberg,Kristiina Airola,Christer Holmberg,Albert de la Chapelle,Juha Kere	329
20	Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3 1995 ·Human Molecular Genetics ·Maria Bitner‐Glindzicz,Peter D. Turnpenny,Pia Höglund,Helena Kääriäinen,Eeva‐Marja Sankila,Silvère M. van der Maarel,Yvette J.M. de Kok,Hans‐Hilger Ropers,Frans P.M. Cremers,(unknown),S Malcolm	58

About Pia Höglund

Pia Höglund is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Nephrology, having authored 27 papers that have together received 1.4k indexed citations. Recurring topics across this work include Ion Transport and Channel Regulation (14 papers), Helicobacter pylori-related gastroenterology studies (11 papers) and Potassium and Related Disorders (9 papers). The work is most often cited by research in Sensory Systems (100 citations), Gastroenterology (101 citations) and Molecular Biology (867 citations). Pia Höglund has collaborated with scholars based in Finland, Sweden and United States. Frequent co-authors include Juha Kere, Christer Holmberg, Siru Haila, Albert de la Chapelle, Siru Mäkelä, Jerzy Socha, Kristiina Airola, Ulpu Saarialho‐Kere, L Tomaszewski and Marja‐Liisa Karjalainen‐Lindsberg. Their work appears in journals such as Nature Genetics, Oncogene and Scientific Reports.

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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