ScholarIQanswers from OpenAlex & ORCID
Susanne Petri
ResearcherPublications, citations & collaboration network
Susanne Petri is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Susanne Petri have?
ScholarIQindexed works
Susanne Petri has 410 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Susanne Petri have?
ScholarIQcitation count
Susanne Petri has 25,020 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Susanne Petri?
ScholarIQh-index
Susanne Petri has an h-index of 65 in OpenAlex.
What is the i10-index of Susanne Petri?
ScholarIQi10-index
Susanne Petri has an i10-index of 227 in OpenAlex.
What is the ORCID of Susanne Petri?
ScholarIQorcid
The ORCID for Susanne Petri is on the source record.
What is the OpenAlex record for Susanne Petri?
ScholarIQopenalex
The OpenAlex for Susanne Petri is on the source record.
What are the most-cited papers on Susanne Petri?
ScholarIQmost cited works
Association of Anxiety-Related Traits with a Polymorphism in the Serotonin Transporter Gene Regulatory Region
Klaus‐Peter Lesch, Dietmar Bengel, Armin Heils, Sue Z. Sabol, Benjamin D. Greenberg, Susanne Petri, Jonathan Benjamin, Clemens R. Müller, Dean H. Hamer, Dennis L. Murphy
Allelic Variation of Human Serotonin Transporter Gene Expression
Armin Heils, Andreas Teufel, Susanne Petri, Gerald Stöber, Peter Riederer, Dietmar Bengel, Klaus‐Peter Lesch
EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) – revised report of an EFNS task force
The EFNS Task Force on Diagnosis and Management of Amyotrophic Lateral Sclerosis:, Peter M. Andersen, Sharon Abrahams, Gian Domenico Borasio, Mamede de Carvalho, Adriano Chiò, Philip Van Damme, Orla Hardiman, Katja Kollewe, Karen Morrison, Susanne Petri, Pierre‐François Pradat, Vincenzo Silani, Barbara Tomik, Maria Wasner, Markus Weber
Amyotrophic lateral sclerosis
Eva L. Feldman, Stephen A. Goutman, Susanne Petri, Letizia Mazzini, Masha G. Savelieff, Pamela J. Shaw, Gen Sobue
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
PARALS Registry, Wouter van Rheenen, SLALOM Group, SLAP Registry, NNIPPS Study Group, Aleksey Shatunov, Annelot M. Dekker, Russell L. McLaughlin, Frank P. Diekstra, Sara L. Pulit, Rick A. A. van der Spek, Urmo Võsa, Simone de Jong, Matthew R. Robinson, Jian Yang, Isabella Fogh, Perry Tc van Doormaal, Gijs Tazelaar, Max Koppers, Anna M. Blokhuis, William Sproviero, Ashley R Jones, Kevin P. Kenna, Kristel R. van Eijk, Oliver Harschnitz, Raymond D. Schellevis, William J. Brands, Jelena Medic, Androniki Menelaou, Alice Vajda, Nicola Ticozzi, Kuang Lin, Boris Rogelj, Katarina Vrabec, Metka Ravnik‐Glavač, Blaž Koritnik, Janez Zidar, Lea Leonardis, Leja Dolenc Grošelj, Stéphanie Millecamps, François Salachas, Vincent Meininger, Mamede de Carvalho, Susana Pinto, Jesús S. Mora, Ricardo Rojas-García, Meraida Polak, Siddharthan Chandran, Shuna Colville, Robert Swingler, Karen Morrison, Pamela J. Shaw, John Hardy, Richard W. Orrell, Alan Pittman, Katie Sidle, Pietro Fratta, Andrea Malaspina, Simon Topp, Susanne Petri, Susanne Abdulla, Carsten Drepper, Michael Sendtner, Thomas Meyer, Roel A. Ophoff, Kim A. Staats, Martina Wiedau‐Pazos, Catherine Lomen‐Hoerth, Vivianna M. Van Deerlin, John Q. Trojanowski, Lauren Elman, Leo McCluskey, A. Nazlı Başak, Ceren Tunca, Hamid Hamzeiy, Yeşim Parman, Thomas Meitinger, Peter Lichtner, Milena Radivojkov‐Blagojevic, Christian Andrés, Cindy Maurel, Gilbert Bensimon, G. Bernhard Landwehrmeyer, Alexis Brice, Christine Payan, Safaa Saker-Delye, Alexandra Dürr, Nicholas Wood, Lukas Tittmann, Wolfgang Lieb, André Franke, Marcella Rietschel, Sven Cichon, Markus M. Nöthen, Philippe Amouyel, Christophe Tzourio, Jean‐François Dartigues, André G. Uitterlinden, Fernando Rivadeneira, Karol Estrada