ScholarIQanswers from OpenAlex
Neuron
JournalCitation impact & published research
Neuron is a journal indexed in ScholarIQ from OpenAlex.
How many works does Neuron have?
ScholarIQindexed works
Neuron has 14,488 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Neuron have?
ScholarIQcitation count
Neuron has 2,833,041 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Neuron?
ScholarIQh-index
Neuron has an h-index of 700 in OpenAlex.
What is the article processing charge of Neuron?
ScholarIQarticle processing charge
Neuron lists an article processing charge of 9,080 USD in OpenAlex.
What is the OpenAlex record for Neuron?
ScholarIQopenalex
The OpenAlex for Neuron is on the source record.
What are the most-cited papers on Neuron?
ScholarIQmost cited works
Whole Brain Segmentation
Bruce Fischl, David H. Salat, Evelina Busa, Marilyn Albert, Megan Dieterich, Christian Haselgrove, André van der Kouwe, Ronald Killiany, David N. Kennedy, Shuna Klaveness, Albert Montillo, Nikos Makris, Bruce R. Rosen, Anders M. Dale
Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
Mariely DeJesus‐Hernandez, Ian R. Mackenzie, Bradley F. Boeve, Adam L. Boxer, Matt Baker, Nicola J. Rutherford, Alexandra M. Nicholson, NiCole A. Finch, Heather C. Flynn, Jennifer Adamson, Naomi Kouri, Aleksandra Wojtas, Pheth Sengdy, Ging‐Yuek Robin Hsiung, Anna Karydas, William W. Seeley, Keith A. Josephs, Giovanni Coppola, Daniel H. Geschwind, Zbigniew K. Wszołek, Howard Feldman, David S. Knopman, Ronald C. Petersen, Bruce L. Miller, Dennis W. Dickson, Khrista Boylan, Neill R. Graff‐Radford, Rosa Rademakers
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
Alan E. Renton, Elisa Majounie, Adrian J. Waite, Javier Simón‐Sánchez, Sara Rollinson, J. Raphael Gibbs, Jennifer C. Schymick, Hannu Laaksovirta, John C. van Swieten, Liisa Myllykangas, Hannu Kalimo, Anders Paetau, Yevgeniya Abramzon, Anne M. Remes, Alice Kaganovich, Sonja W. Scholz, Jamie Duckworth, Jinhui Ding, Daniel W. Harmer, Dena G. Hernandez, Janel O. Johnson, Kin Y. Mok, Mina Ryten, Daniah Trabzuni, Rita Guerreiro, Richard W. Orrell, James Neal, Alex Murray, Justin Pearson, Iris E. Jansen, David Sondervan, Harro Seelaar, Derek J. Blake, Kate Young, Nicola Halliwell, Janis Bennion Callister, Greg Toulson, Anna Richardson, Alexander Gerhard, Julie S. Snowden, David Mann, David Neary, Michael A. Nalls, Terhi Peuralinna, Lilja Jansson, Veli‐Matti Isoviita, Anna-Lotta Kaivorinne, Maarit Hölttä‐Vuori, Elina Ikonen, Raimo Sulkava, Michael Benatar, Joanne Wuu, Adriano Chiò, Gabriella Restagno, Giuseppe Borghero, Mario Sabatelli, David Heckerman, Ekaterina Rogaeva, Lorne Zinman, Jeffrey D. Rothstein, Michael Sendtner, Carsten Drepper, Evan E. Eichler, Can Alkan, Ziedulla Abdullaev, Svetlana Pack, Amalia Dutra, Evgenia Pak, John Hardy, Andrew Singleton, Nigel Williams, Peter Heutink, Stuart Pickering‐Brown, Huw R. Morris, Pentti J. Tienari, Bryan J. Traynor
Functional Network Organization of the Human Brain
Jonathan D. Power, Alexander L. Cohen, Steven M. Nelson, Gagan S. Wig, Kelly A. Barnes, Jessica A. Church, Alecia C. Vogel, Timothy O. Laumann, Fran M. Miezin, Bradley L. Schlaggar, Steven E. Petersen
Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
Alexander Zimprich, Saskia Biskup, Petra Leitner, Peter Lichtner, Matthew J. Farrer, Sarah Lincoln, Jennifer M. Kachergus, Mary Hulihan, Ryan J. Uitti, Donald B. Calne, A. Jon Stoessl, Ronald F. Pfeiffer, Nadja Patenge, Iria Carballo‐Carbajal, P. Vieregge, Friedrich Asmus, Bertram Müller‐Myhsok, Dennis W. Dickson, Thomas Meitinger, Tim M. Strom, Zbigniew K. Wszołek, Thomas Gasser