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论文共 48 篇作者统计合作学者相似作者

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Extremely Rare CNVs Contributing to Alzheimer Disease Risk: a Case-Control Association Analysis of Exome Sequencing Data from 22,319 Individuals
Olivier Quenez,Catherine Schramm,Kevin Cassinari,Aude Nicolas, Joan Groeneveld,Guillaume Huguet,Benjamin Grenier-Boley,Marc Hulsman,Anne-Claire Richard,Stéphane Rousseau,Shahzad Ahmad,Najaf Amin,Philippe Amouyel, Olivia Belbin,Céline Bellenguez,Claudine Berr,Anne Boland,Paola Bossù,Femke Bouwman,Jose Bras,Jordi Clarimon,Antonio Daniele,Jean-François Dartigues,Stéphanie Debette,Jean-François Deleuze,Nicola Denning,Oriol Dols-Icardo, Cornelia M, van Dujin, Victoria Fernandez,Wiesje M. van der Flier,Juan Fortea,Nick C. Fox,Ruth Frikke-Schmidt,Daniela Galimberti,Emmanuelle Genin,Roberta Ghidoni,Vilmantas Giedraitis, Johan J. P. Gille,Detelina Grozeva,Rita Guerreiro,Edna Grünblatt,John Hardy,Steffi G. Riedel-Heller,Mikko Hiltunen,Clive Holmes,Henne Holstege,Jakub Hort,Holger Hummerich,M. Arfan Ikram,M. Kamran Ikram,Martin Ingelsson,Iris E. Jansen,Amit Kawalia,Robert Kraaij,Patrick G. Kehoe, Marc Lathrop,Morgane Lacour,Afina W. Lemstra,Alberto Lleò,Lauren Luckcuck,Marcel M. A. M. Mannens,Rachel Marshall,Carlo Masullo,Simon Mead,Patrizia Mecocci,Alexandre de Mendonça,Alun Meggy,Shima Mehrabian,Merel O. Mol,Kevin Morgan,Alexandre Morin,Benedetta Nacmias,Penny J. Norsworthy,Florence Pasquier,Pau Pastor, Fabrizio Piras,Julius Popp,Alfredo Ramirez,Rachel Raybould,Richard Redon,Marcel J. T. Reinders,Fernando Rivadeneira,Jeroen G. J. van Rooij,Natalie S. Ryan,Salha Saad,Pascual Sanchez-Juan,Nikolaos Scarmeas,Philip Scheltens,Jonathan M. Schott,Davide Seripa,Daoud Sie,Rebecca Sims, Erik A. Sistermans,Sandro Sorbi,Kristel Sleegers,Resie van Spaendonk,John C. van Swieten,Niccolo Tesi, Betty M Tijms,André G. Uitterlinden,Magda Tsolaki,Pieter Jelle Visser,Michael Wagner,Julie Williams,Aline Zarea,David Wallon, Sébastien Jacquemont,Jean-Charles Lambert,Sven J. van der Lee,Camille Charbonnier,Gaël Nicolas
crossref（2024）
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Exome Sequencing Identifies Rare Damaging Variants in ATP8B4 and ABCA1 As Risk Factors for Alzheimer’s Disease
Henne Holstege,Marc Hulsman,Camille Charbonnier,Benjamin Grenier-Boley,Olivier Quenez,Detelina Grozeva,Jeroen G. J. van Rooij,Rebecca Sims,Shahzad Ahmad,Najaf Amin,Penny J. Norsworthy,Oriol Dols-Icardo,Holger Hummerich,Amit Kawalia,Philippe Amouyel,Gary W. Beecham,Claudine Berr,Joshua C. Bis,Anne Boland,Paola Bossù,Femke Bouwman,Jose Bras,Dominique Campion,J. Nicholas Cochran,Antonio Daniele,Jean-François Dartigues,Stéphanie Debette,Jean-François Deleuze,Nicola Denning,Anita L. DeStefano,Lindsay A. Farrer,Maria Victoria Fernández,Nick C. Fox,Daniela Galimberti,Emmanuelle Genin, Johan J. P. Gille,Yann Le Guen,Rita Guerreiro,Jonathan L. Haines,Clive Holmes,M. Arfan Ikram,M. Kamran Ikram,Iris E. Jansen,Robert Kraaij, Marc Lathrop,Afina W. Lemstra,Alberto Lleó,Lauren Luckcuck,Marcel M. A. M. Mannens,Rachel Marshall,Eden R. Martin,Carlo Masullo,Richard Mayeux,Patrizia Mecocci,Alun Meggy,Merel O. Mol,Kevin Morgan,Richard M. Myers,Benedetta Nacmias,Adam C. Naj,Valerio Napolioni,Florence Pasquier,Pau Pastor,Margaret A. Pericak-Vance,Rachel Raybould,Richard Redon,Marcel J. T. Reinders,Anne-Claire Richard,Steffi G. Riedel-Heller,Fernando Rivadeneira,Stéphane Rousseau,Natalie S. Ryan,Salha Saad,Pascual Sanchez-Juan,Gerard D. Schellenberg,Philip Scheltens,Jonathan M. Schott,Davide Seripa,Sudha Seshadri,Daoud Sie,Erik A. Sistermans,Sandro Sorbi,Resie van Spaendonk,Gianfranco Spalletta,Niccolo’ Tesi,Betty Tijms,André G. Uitterlinden,Sven J. van der Lee,Pieter Jelle Visser,Michael Wagner,David Wallon,Li-San Wang,Aline Zarea,Jordi Clarimon,John C. van Swieten,Michael D. Greicius,Jennifer S. Yokoyama,Carlos Cruchaga,John Hardy,Alfredo Ramirez,Simon Mead,Wiesje M. van der Flier,Cornelia M. van Duijn,Julie Williams,Gaël Nicolas,Céline Bellenguez,Jean-Charles Lambert
Nature Genetics（2022）
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作者统计

#Papers: 48

#Citation: 2872

H-Index: 23

G-Index: 35

Sociability: 6

Diversity: 3

Activity: 12

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