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Olli Pietiläinen

ResearcherPublications, citations & collaboration network

Olli Pietiläinen is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Olli Pietiläinen have?

ScholarIQindexed works

Olli Pietiläinen has 201 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Olli Pietiläinen have?

ScholarIQcitation count

Olli Pietiläinen has 26,196 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Olli Pietiläinen?

ScholarIQh-index

Olli Pietiläinen has an h-index of 51 in OpenAlex.

What is the i10-index of Olli Pietiläinen?

ScholarIQi10-index

Olli Pietiläinen has an i10-index of 112 in OpenAlex.

What is the ORCID of Olli Pietiläinen?

ScholarIQorcid

The ORCID for Olli Pietiläinen is on the source record.

What is the OpenAlex record for Olli Pietiläinen?

ScholarIQopenalex

The OpenAlex for Olli Pietiläinen is on the source record.

What are the most-cited papers on Olli Pietiläinen?

ScholarIQmost cited works
Large recurrent microdeletions associated with schizophrenia
GROUP, Hreinn Stefánsson, Dan Rujescu, Sven Cichon, Olli Pietiläinen, Andrés Ingason, Stacy Steinberg, Ragnheiður Fossdal, Engilbert Sigurðsson, Thordur Sigmundsson, Jacobine E. Buizer‐Voskamp, Thomas Folkmann Hansen, Klaus D. Jakobsen, Pierandrea Muglia, Clyde Francks, Paul M. Matthews, Arnaldur Gylfason, Bjarni V. Halldórsson, Daníel F. Guðbjartsson, Thorgeir E. Thorgeirsson, Ásgeir Sigurðsson, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ásgeir Björnsson, Sigurborg Mattiasdottir, Thórarinn Blöndal, Magnús Haraldsson, Brynja B. Magnúsdóttir, Ina Giegling, Hans‐Jürgen Möller, Annette M. Hartmann, Kevin V. Shianna, Dongliang Ge, Anna C. Need, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamarie Tuulio-Henriksson, Tiina Paunio, Timi Toulopoulou, Elvira Bramon, Marta Di Forti, Robin Murray, Mirella Ruggeri, Evangelos Vassos, Sarah Tosato, Muriel Walshe, Tao Li, Catalina Vasilescu, Thomas W. Mühleisen, August G. Wang, Henrik Ullum, Srdjan Djurovic, Ingrid Melle, Jes Olesen, Lambertus A. Kiemeney, Barbara Franke, Chiara Sabatti, Nelson B. Freimer, Jeffrey R. Gulcher, Unnur Þorsteinsdóttir, Augustine Kong, Ole A. Andreassen, Roel A. Ophoff, Alexander Georgi, Marcella Rietschel, Thomas Werge, Hannes Pétursson, David B. Goldstein, Markus M. Nöthen, Leena Peltonen, David Collier, David St Clair, Kāri Stefánsson
Nature. 20081,778 CitationsOPEN ACCESS
Common variants conferring risk of schizophrenia
†Genetic Risk and Outcome in Psychosis (GROUP), Hreinn Stefánsson, Roel A. Ophoff, Stacy Steinberg, Ole A. Andreassen, Sven Cichon, Dan Rujescu, Thomas Werge, Olli Pietiläinen, Ole Mors, Preben Bo Mortensen, Engilbert Sigurðsson, Ómar Gústafsson, Mette Nyegaard, Annamari Tuulio‐Henriksson, Andrés Ingason, Thomas Folkmann Hansen, Jaana Suvisaari, Jouko Lönnqvist, Tiina Paunio, Anders D. Børglum, Annette M. Hartmann, Anders Fink‐Jensen, Merete Nordentoft, David M. Hougaard, Bent Nørgaard‐Pedersen, Yvonne Böttcher, Jes Olesen, René Breuer, Hans‐Jürgen Möller, Ina Giegling, Henrik B. Rasmussen, Sally Timm, Manuel Mattheisen, István Bitter, János Réthelyi, Brynja B. Magnúsdóttir, Thordur Sigmundsson, Pall I. Olason, Gísli Másson, Jeffrey R. Gulcher, Magnús Haraldsson, Ragnheiður Fossdal, Thorgeir E. Thorgeirsson, Unnur Þorsteinsdóttir, Mirella Ruggeri, Sarah Tosato, Barbara Franke, Eric Strengman, Lambertus A. Kiemeney, Ingrid Melle, Srdjan Djurovic, Л. И. Абрамова, В. Г. Каледа, Julio Sanjuán, Rosa de Frutos, Elvira Bramon, Evangelos Vassos, Gillian Fraser, Ulrich Ettinger, Marco Picchioni, Nicholas Walker, Timi Toulopoulou, Anna C. Need, Dongliang Ge, Joeng Lim Yoon, Kevin V. Shianna, Nelson B. Freimer, Rita M. Cantor, Robin Murray, Augustine Kong, В. Е. Голимбет, Ángel Carracedo, Celso Arango, Javier Costas, Erik G. Jönsson, Lars Terenius, Ingrid Agartz, Hannes Pétursson, Markus M. Nöthen, Marcella Rietschel, Paul M. Matthews, Pierandrea Muglia, Leena Peltonen, David St Clair, David B. Goldstein, Kāri Stefánsson, David Collier
Nature. 20091,720 CitationsOPEN ACCESS
Disruption of the neurexin 1 gene is associated with schizophrenia
Dan Rujescu, Andrés Ingason, Sven Cichon, Olli Pietiläinen, Michael R. Barnes, Timothea Toulopoulou, Marco Picchioni, Evangelos Vassos, Ulrich Ettinger, Elvira Bramon, Robin Murray, Mirella Ruggeri, Sarah Tosato, Chiara Bonetto, Stacy Steinberg, Engilbert Sigurðsson, Thordur Sigmundsson, Hannes Pétursson, Arnaldur Gylfason, Pall I. Olason, Gudmundur Hardarsson, Guðrún A. Jónsdóttir, Ómar Gústafsson, Ragnheiður Fossdal, Ina Giegling, Hans‐Jürgen Möller, Annette M. Hartmann, Per Hoffmann, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Srdjan Djurovic, Ingrid Melle, Ole A. Andreassen, Thomas Folkmann Hansen, Thomas Werge, Lambertus A. Kiemeney, Barbara Franke, Joris A. Veltman, Jacobine E. Buizer‐Voskamp, GROUP Investigators, Chiara Sabatti, Roel A. Ophoff, Marcella Rietschel, Markus M. Nöthen, Kāri Stefánsson, Leena Peltonen, David St Clair, Hreinn Stefánsson, David Collier
Human Molecular Genetics. 2008489 CitationsOPEN ACCESS
Copy number variations of chromosome 16p13.1 region associated with schizophrenia
Andrés Ingason, Dan Rujescu, Sven Cichon, Engilbert Sigurðsson, Thordur Sigmundsson, Olli Pietiläinen, Jacobine E. Buizer‐Voskamp, E Strengman, Clyde Francks, Pierandrea Muglia, Arnaldur Gylfason, Ómar Gústafsson, Pall I. Olason, Stacy Steinberg, Thomas Folkmann Hansen, Klaus D. Jakobsen, Henrik B. Rasmussen, Ina Giegling, HJ Möller, A. Hartmann, Caroline Crombie, G. T. Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Elvira Bramon, Lambertus A. Kiemeney, Barbara Franke, Robin Murray, Evangelos Vassos, Timothea Toulopoulou, Thomas W. Mühleisen, Sarah Tosato, Mirella Ruggeri, Srdjan Djurovic, Ole A. Andreassen, Z Zhang, Thomas Werge, Roel A. Ophoff, GROUP Investigators, Marcella Rietschel, Markus M. Nöthen, Hannes Pétursson, Hreinn Stefánsson, Laura‐Maria Peltonen, David Collier, Hreinn Stefánsson, David M. St. Clair
Molecular Psychiatry. 2009266 CitationsOPEN ACCESS
Common variants at VRK2 and TCF4 conferring risk of schizophrenia
Stacy Steinberg, Simone de Jong, Ole A. Andreassen, Thomas Werge, Anders D. Børglum, Ole Mors, Preben Bo Mortensen, Ómar Gústafsson, Javier Costas, Olli Pietiläinen, Ditte Demontis, Sergi Papiol, Johanna Huttenlocher, Manuel Mattheisen, René Breuer, Evangelos Vassos, Ina Giegling, Gillian Fraser, Nicholas Walker, Annamari Tuulio‐Henriksson, Jaana Suvisaari, Jouko Lönnqvist, Tiina Paunio, Ingrid Agartz, Ingrid Melle, Srdjan Djurovic, Eric Strengman, Gesche Jűrgens, Birte Glenthøj, Lars Terenius, David M. Hougaard, Torben Ørntoft, Carsten Wiuf, Michael Didriksen, Mads V. Hollegaard, Merete Nordentoft, Ruud van Winkel, Günter Kenis, Л. И. Абрамова, В. Г. Каледа, Manuel Arrojo, Julio Sanjuán, Celso Arango, Swetlana Sperling, Moritz J. Rossner, Michele Ribolsi, Valentina Magni, Alberto Siracusano, Claus Christiansen, Lambertus A. Kiemeney, Jan H. Veldink, Leonard van den Berg, Andrés Ingason, Pierandrea Muglia, Robin Murray, Markus M. Nöthen, Engilbert Sigurðsson, Hannes Pétursson, Unnur Þorsteinsdóttir, Augustine Kong, I. Alex Rubino, Marc De Hert, János Réthelyi, István Bitter, Erik G. Jönsson, В. Е. Голимбет, Ángel Carracedo, Hannelore Ehrenreich, Nick Craddock, Michael J. Owen, Michael O‘Donovan, Mirella Ruggeri, Sarah Tosato, Leena Peltonen, Roel A. Ophoff, David Collier, David St Clair, Marcella Rietschel, Sven Cichon, Hreinn Stefánsson, Dan Rujescu, Kāri Stefánsson
Human Molecular Genetics. 2011218 CitationsOPEN ACCESS

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