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Reza Maroofian

UCL Queen Square Institute of Neurology

40H指数
318论文数
5.9K被引数
收录论文 211
发表时间
Clinical, genetic, neuroimaging, and severity spectrum of peroxisomal disorders in Iran: a multicenter cohort study伊朗过氧化物酶体障碍的临床、遗传、神经影像及严重程度谱:一项多中心队列研究
err2026-08-12
err0
errOAAI
errGolazin Shahbodagh Khan; Narges Mashayekhi; Shiva Bayat; Mehran Beiraghi Toosi; Sareh Hosseinpour; Neda Pak; Danielle Dircks; Zahra Rezaei; Reza Shervin Badv; Gholam Reza Zamani; Mahmoud Mohammadi; Mojtaba Movahednia; Parvaneh Karimzadeh; Reza Maroofian; Michael C. Kruer; Ehsan Ghayoor Karimiani; Masoud Garshasbi; Mahmoud Reza Ashrafi; Morteza Heidari; Ali Reza Tavasoli
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Turbocharging synaptic transmission: 12 SNAREpins are required for rapid release of reconstituted synaptic vesicles增强突触传递:12个SNAREpin复合体是快速释放重组突触小泡所必需的
err2026-07-01
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errOAAI
errManindra Bera; Atrouli Chatterjee; Amit Koikkarah Aji; Aniruddha Panda; R. Venkat K. Sundaram; Jeff Coleman; Reza Maroofian; Vincenzo Salpietro; Abhijith Radhakrishnan; Sudhanshu Gautam; Kirill Grushin; Matthieu Caruel; Henry Houlden; Kallol Gupta; Sathish Ramakrishnan; Frederic Pincet; James E. Rothman
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COXFA4L2 upregulation preserves residual cytochrome c oxidase activity in COXFA4-related Leigh-like encephalopathyCOXFA4L2上调在COXFA4相关 Leigh样脑病中维持残余细胞色素c氧化酶活性
err2026-05-30
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errOAAI
errMicol Falabella; Sandra Lopez Calcerrada; Jana Aref; Jiaze Gao; William L. Macken; Chiara Pizzamiglio; Renata Kabiljo; Anna Lucia Francavilla; Pauline Gaignard; Antoine Pouzet; Jonathan Levy; Giulia Barcia; Jamie K. Leighton; Efstathia Chronopoulou; Germaine Pierre; Riza Köksal Özgül; Ali Dursun; Rebecca Halligan; Helen Mundy; Javeria Raza Alvi; Tipu Sultan; William James Craigen; Lisa Emrick; Jill A. Rosenfeld; Gehad Elmakkawy; JiHye Kim; Joseph J. Gleeson; Aboulfazl Rad; Gabriela Oprea; Maqbool Hussain; Khalil Ur Rehman; Sadia Riaz; Robert W. Taylor; Vincent Procaccio; Maha S. Zaki; Erika Fernandez-Vizarra; Ciro Leonardo Pierri; Michael G. Hanna; Henry Houlden; Reza Maroofian; Cristina Ugalde; Jan-Willem Taanman; Robert D. S. Pitceathly
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Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethality蛋白酶体调节因子PSMF1的变异导致从帕金森病到围产期死亡表型谱
err2026-04-15
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errOAAI
errFrancesca Magrinelli; Christelle Tesson; Plamena R. Angelova; Jose A. Rodriguez; Annarita Scardamaglia; Benjamin O’Callaghan; Simon A. Lowe; Ainara Salazar-Villacorta; Brian Hon-Yin Chung; Matthew Jaconelli; Barbara Vona; Noemi Esteras; Angela Mammana; Junko Shimazu; Anna Ka-Yee Kwong; Thomas Courtin; Shahryar Alavi; Reza Maroofian; Raja Nirujogi; Mariasavina Severino; Edoardo Monfrini; Clarissa Rocca; Patrick A. Lewis; Stephanie Efthymiou; Rebecca Buchert; Linda Sofan; Pawel Lis; Chloé Pinon; Guido J. Breedveld; Martin Man-Chun Chui; David Murphy; Vanessa Pitz; Mary B. Makarious; Simone Baiardi; Marina Volin; Marlene Cassar; Bassem A. Hassan; Sana Iftikhar; Peter Bauer; Michele Tinazzi; Marina Svetel; Bedia Samanci; Haşmet A. Hanağası; Basar Bilgiç; Francesco Cavallieri; Mario Santangelo; José A. Obeso; Monica M. Kurtis; Guillaume Cogan; Güneş Kiziltan; Tuğçe Gül-Demirkale; Hülya Tireli; Gülbün A. Yüksel; Gül Yalçın-Cakmakli; Bülent Elibol; Nina Barišić; Earny Wei-Sen Ng; Sze-Shing Fan; Tova Hershkovitz; Karin Weiss; Javeria Raza Alvi; Tipu Sultan; Issam Azmi Alkhawaja; Tawfiq Froukh; Hadeel Abdollah E. Alrukban; Muhammad Nadeem Anjum; Anjum Saeed; Huma Arshad Cheema; Christine Fauth; Ulrich A. Schatz; Thomas Zöggeler; Michael Zech; Karen Stals; Vinod Varghese; Sonia Gandhi; Cornelis Blauwendraat; John A. Hardy; Alessio Di Fonzo; Vincenzo Bonifati; Tobias B. Haack; Aida M. Bertoli-Avella; Suzanne Lesage; Ayşe Nazlı Başak; Robert Steinfeld; Piero Parchi; James E. C. Jepson; Dario R. Alessi; Alexis Brice; Hermann Steller; Andrey Y. Abramov; Kailash P. Bhatia; Henry Houlden
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DRD1-driven infantile dystonia: towards a mechanism-informed framework for GPCR receptoropathiesDRD1驱动的婴儿期肌张力障碍:构建GPCR受体病的机制导向框架
errBrain
IF11.7
err2026-04-09
err0
PREAI
errGülsüm Kayhan; Ryosuke Tany; Reza Maroofian; Esra Serdaroğlu; Eon Kurumiya; Duy Phuoc Tran; Hideko Wakasugi-Masuho; Mirja Thomsen; Kamran Salayev; Rauan Kaiyrzhanov; Saadat Badalova; Ulviyya Guliyeva; Adel Kareem; Peter Bauer; Giovanni Zifarelli; Henry Houlden; Katja Lohmann; Akio Kitao; M Fatih Mulayim; Ikuo Masuho
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Expanded clinical and genetic characterization of autosomal recessive HMGCR-related muscular dystrophy常染色体隐性HMGCR相关肌营养不良的临床与遗传学特征扩展研究
err2026-03-29
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PREAI
errStephany El-Hayek; Aboulfazl Rad; Sahar Sedighzadeh; Gozde Yesil; Sandra Sabbagh; Mohammad Shahrooei; Pratibha Nair; Asuman Gedikbaşı; Sami Bizzari; Murtadha Ali; Eliane Chouery; Cybel Mehawej; Ayca Aslanger; Pejman Rohani; Meisam Sharifzadeh; Sinan Akbas; Javad Mohammadi-asl; Mahdiyeh Behnam; Sandra Corbani; Volkan Karaman; Uluç Yiş; Yavuz Oktay; Ipek Polat; J Andoni Urtizberea; Henry Houlden; Reza Maroofian; Gabriela Oprea; Andre Megarbane
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Expansion of Molecular and Clinical Aspects of EPS8L2 (DFNB106)-Associated Hearing Loss Emphasizes a Potential Therapeutic WindowEPS8L2 (DFNB106)相关听力损失的分子和临床方面扩展强调了潜在的治疗窗口
err2026-01-10
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errOAAI
errDaniel Owrang; Aboulfazl Rad; Masoome Alerasool; Susanne M. Kolb; Sheng-Jia Lin; Julia Doll; Neda Alidadiani; Shahrooz Ghaderi; Michaela A. H. Hofrichter; Reza Maroofian; Gaurav K. Varshney; Majid Mojarrad; Oliver Bartsch; Thomas Haaf; Barbara Vona
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Neurodevelopmental Disease-causing Variants in Choline Kinase CHKA Gene Couple Phosphatidylcholine Synthesis to Oxidative Stress Damage and Disease Etiology神经发育性疾病致病变异在胆碱激酶CHKA基因中,将磷脂酰胆碱合成与氧化应激损伤及疾病病因相耦合。
err2025-11-25
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errOAAI
errMahtab Tavasoli; Mariam Alkandari; Gabriel Dorighello; Michael McPhee; Neale D. Ridgway; Kathy Isaac; Stanislav Sokolenko; Reza Maroofian; Anju Shukla; Maha S. Zaki; Henry Houlden; Christopher R. McMaster
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Letter Concerning Biallelic Variants in EPG5 Gene Are Associated with Parkinson's Disease关于EPG5基因中的双等位基因变异与帕金森病相关性的信件
err2025-10-29
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PREAI
errHormos Salimi Dafsari MD; Celine Deneubourg PhD; Kritarth Singh PhD; Reza Maroofian PhD; Michael R. Duchen PhD; Adam Antebi PhD; Henry Houlden MD, PhD; Manolis Fanto PhD; Heinz Jungbluth MD, PhD
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Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function致病性UNC13A变异通过损害突触功能导致神经发育综合征
err2025-10-22
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errOAAI
errReza Asadollahi; Aisha Ahmad; Paranchai Boonsawat; Jasmine Shahanoor Hinzen; Mareike Lohse; Boris Bouazza-Arostegui; Siqi Sun; Tillmann Utesch; Jonas D. Sommer; Dragana Ilic; Murugesh Padmanarayana; Kati Fischermanns; Mrinalini Ranjan; Moritz Boll; Chandran Ka; Amélie Piton; Francesca Mattioli; Bertrand Isidor; Katrin Õunap; Karit Reinson; Monica H. Wojcik; Christian R. Marshall; Saadet Mercimek-Andrews; Naomichi Matsumoto; Noriko Miyake; Bruno de Oliveira Stephan; Rachel Sayuri Honjo; Debora R. Bertola; Chong Ae Kim; Roman Yusupov; Heather C. Mefford; John Christodoulou; Joy Lee; Oliver Heath; Natasha J. Brown; Naomi Baker; Zornitza Stark; Martin Delatycki; Nicole J. Lake; Shimriet Zeidler; Linda Zuurbier; Saskia M. Maas; Chris C. de Kruiff; Farrah Rajabi; Lance H. Rodan; Stephanie A. Coury; Konrad Platzer; Henry Oppermann; Rami Abou Jamra; Skadi Beblo; Caroline Maxton; Robert Śmigiel; Hunter Underhill; Holly Dubbs; Alyssa Rosen; Katherine L. Helbig; Ingo Helbig; Sarah McKeown Ruggiero; Mark P. Fitzgerald; Dennis Kraemer; Carlos E. Prada; Jeffrey Tenney; Parul Jayakar; Sylvia Redon; Jérémie Lefranc; Kevin Uguen; Simone Race; Stephanie Efthymiou; Reza Maroofian; Henry Houlden; Sandra Coppens; Nicolas Deconinck; Balasubramaniem Ashokkumar; Perumal Varalakshmi; Vykunta Raju Gowda K; Fatemeh Eghbal; Ehsan Ghayoor Karimiani; Morteza Heidari; John Neidhardt; Marta Owczarek-Lipska; G. Christoph Korenke; Michael J. Bamshad; Philippe M. Campeau; Anna Lehman; Laura G. Hendon; Ingrid M. Wentzensen; Kristin G. Monaghan; Yanmin Chen; Anna Szuto; Ronald D. Cohn; Ping Yee Billie Au; Christoph Hübner; Felix Boschann; Kandamurugu Manickam; Daniel C. Koboldt; Aboulfazl Rad; Gabriela Oprea; Kristine K. Bachman; Andrea H. Seeley; Emanuele Agolini; Alessandra Terracciano; Piscopo Carmelo; Caleb Bupp; Bethany Grysko; Annick Rein-Rothschild; Bruria Ben Zeev; Amy Margolin; Jennifer Morrison; Aditi Dagli; Elliot Stolerman; Raymond J. Louie; Camerun Washington; Servi J. C. Stevens; Malou Heijligers; Fowzan S. Alkuraya; Jasmin Lisfeld; Axel Neu; Fabíola Paoli Monteiro; André Luiz Santos Pessoa; Antonio Edvan Camelo-Filho; Fernando Kok; Dwight Koeberl; Kacie Riley; Lydie Burglen; Diane Doummar; Bénédicte Héron; Cyril Mignot; Boris Keren; Perrine Charles; Caroline Nava; Felix P. Bernhard; Andrea A. Kühn; Sven Thoms; Ryan D. Morrie; Shila Mekhoubad; Eric M. Green; Sami J. Barmada; Aaron D. Gitler; Olaf Jahn; Jeong Seop Rhee; Christian Rosenmund; Mišo Mitkovski; Heinrich Sticht; Han Sun; Gerald Le Gac; Holger Taschenberger; Nils Brose; Jeremy S. Dittman; Anita Rauch; Noa Lipstein
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RRP12 Variants Are Associated With Autosomal Recessive Brain CalcificationsRRP12 变体与常染色体隐性脑钙化相关
err2025-10-08
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errOAAI
errEdoardo Monfrini MD, PhD; Paola Rinchetti PhD; Mathieu Anheim MD, PhD; Anna Klingseisen PhD; Ouhaid Lagha-Boukbiza MD; Zhidong Cen MD, PhD; Dehao Yang MD, PhD; Xinhui Chen MD; Reza Maroofian PhD; Henry Houlden MD, PhD, FRCP, FRCPath, FMedSci; Gioia Cappelletti PhD; Anne-Claire Richard BS; Olivier Quenez PhD; Camilo Toro MD; Steven J. Frucht MD; Francesco Lotti PhD; Wei Luo MD, PhD; David Hunt MD, PhD; Gael Nicolas MD, PhD; Giulietta M. Riboldi MD, PhD
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EIPR1 variants cause a neurodevelopmental disorder with endolysosomal and dense core vesicle defectsEIPR1基因变异导致伴有内体-溶酶体和致密核心囊泡缺陷的神经发育障碍
errBrain
IF11.7
err2025-10-07
err0
PREAI
errSaikat Ghosh; Jaskaran Singh; Nadirah S Damseh; Mariasavina Severino; Raffaella De Pace; Adriana E Golding; Michal Jarnik; Poonam Thakran; Laurence Faivre; Jade Heitz; Anne-Sophie Denommé-Pichon; Antonio Vitobello; Lama AlAbdi; Firdous Abdulwahab; Safia Sumayli; Mashael Alqahtani; Huma Arshad Cheema; Iram Javed; JiHye Kim; Hanns Lochmüller; Hagar Mor-Shaked; Jennifer E Neil; Ganeshwaran H Mochida; Giovanni Zifarelli; Peter Bauer; Ehsan Barkhordari; Ehsan Ghayoor Karimiani; Henry Houlden; Bassam Abu-Libdeh; Simon Edvardson; Orly Elpeleg; Reza Maroofian; Shunmoogum A Patten; Juan S Bonifacino
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Comprehensive Genotypic, Phenotypic, and Biochemical Characterization of GOT2 Deficiency: A Progressive Neurodevelopmental Disorder with Epilepsy and Abnormal MovementsGOT2缺乏症的全面基因型、表型及生化表征:一种伴有癫痫和异常运动的进行性神经发育障碍
err2025-09-23
err0
PREAI
errHannah M. German; Maha S. Zaki; Muhammad A. Usmani; Irem Karagoz; Stephanie Efthymiou; Mohamed S. Abdel-Hamid; Haya Abdelhafez Arabiyat; Amama Ghaffar; Mohsin Shahzad; Hans van Bokhoven; Zubair M. Ahmed; Omid Yaghini; Neda Hosseini; Maede Majidinezhad; Shahryar Alavi; Marjolein Bosma; Melissa H. Broeks; Dilşad Türdoğan; Mohnish Suri; Laiz Laura de Godoy; Nanda M. Verhoeven-Duif; Sheikh Riazuddin; Joseph G. Gleeson; Cesar Alves; Judith J.M. Jans; Saima Riazuddin; Henry Houlden; Reza Maroofian
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A clinical and genotype-phenotype analysis of MACF1 variantsMACF1变异的临床与基因型-表型分析
err2025-09-08
err0
PREAI
errJordy Dekker; Rachel Schot; Kimberly A. Aldinger; David B. Everman; Camerun Washington; Julie R. Jones; Jennifer A. Sullivan; Rebecca C. Spillmann; Vandana Shashi; Antonio Vitobello; Anne-Sophie Denommé-Pichon; Anne-Laure Mosca-Boidron; Laurence Perrin; Stéphane Auvin; Maha S. Zaki; Joseph G. Gleeson; Naomi Meave; Cassidy Wallace; Sophie Nambot; Julian Delanne; Sarah M. Ruggiero; Ingo Helbig; Mark P. Fitzgerald; Richard J. Leventer; Dorothy K. Grange; Emanuela Argilli; Elliott H. Sherr; Supraja Prakash; Derek E. Neilson; Francesco Nicita; Antonella Sferra; Enrico S. Bertini; Chiara Aiello; Knut Brockmann; Alexander B. Kuranov; Silke Kaulfuss; Sulman Basit; Majed Alluqmani; Ahmad Almatrafi; Jan M. Friedman; Colleen Guimond; Faruq Mohammed; Pooja Sharma; Divya Goel; Thomas Wirth; Mathieu Anheim; Paulina Bahena; Asuman Koparir; Konstantinos Kolokotronis; Barbara Vona; Thomas Haaf; Erdmute Kunstmann; Reza Maroofian; Henrike L. Sczakiel; Felix Boschann; Mala Misra-Isrie; Raymond J. Louie; Elliot S. Stolerman; Pedro A. Sanchez-Lara; Sandra Mergler; Renske Oegema; Yuri A. Zarate; Ariana Kariminejad; Homa Tajsharghi; Shimriet Zeidler; Anneke J.A. Kievit; Arjan Bouman; Gerarda Cappuccio; Nicola Brunetti-Pierri; Kyra E. Stuurman; Dayna Morel Swols; Mustafa Tekin; Jariya Upadia; Donna M. Martin; Daniel Craven; Susan M. Hiatt; Laura A. van de Pol; Felice D'Arco; Henri Margot; Martina Wilke; Soheil Yousefi; Tahsin Stefan Barakat; Monique M. van Veghel-Plandsoen; Eleonora Aronica; Jasper Anink; Stephen L. Rogers; Kevin C. Slep; Dan Doherty; William B. Dobyns; Grazia M.S. Mancini
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Bi-Allelic Variants in MICU1 Cause Myopathy With Extrapyramidal Signs: Case Series, Phenotypic Spectrum, and Genotype–Phenotype Correlations From 61 Patients双等位基因变异导致伴有锥体外系体征的肌病:61例患者的病例系列、表型谱和基因型-表型相关性
err2025-09-02
err0
PREAI
errPegah Beheshti; Fahimeh Akbarian; Emran Esmaeilzadeh; Hamid Galehdari; Mehdi Khorrami; Sadeq Vallian; Alireza Abdi; Özge Güngör; Rasim Tuncel; Ayca Aykut; Özgul Ekmekci; Haluk Akın; Asude Durmaz; Atefeh Sohanforooshan Moghaddam; Niloofar Chamanrou; Fatemeh Karimi; Arezu Kazemi; Mahvash Habibi; Mohammad Amin Tabatabaiefar; Hamid Reza Khorram Khorshid; Farshid Parvini; Uluç Yiş; Ipek Polat; Leila Youssefian; Hassan Vahidnezhad; Morteza Heidari; Payam Sarraf; Ehsan Ghayoor Karimiani; Reza Maroofian; Sajjad Biglari
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Clinical and molecular characterization of SLC31A1-related developmental and epileptic encephalopathy: insights from 13 new casesSLC31A1相关的发育性癫痫性脑病的临床与分子特征:13例新病例的启示
err2025-09-01
err0
errOAAI
errNatalia Juliá-Palacios; Gerard Muñoz-Pujol; Reza Maroofian; Aida M Bertoli-Avella; Marta Gómez-Chiari; Jordi Muchart-López; Abraham J Paredes-Fuentes; Mar O’Callaghan; Irene S Machado-Casas; Ingrid Cristian; Jennifer Morrison; Angels Garcia-Cazorla; Anna Codina; Mohammad Miryounesi; Emir Zonic; Peter Bauer; Huma Cheema; Muhammad Nadeem Anjum; Nouriya Al-Sannaa; Marwa Abd Elmaksoud; Faroug Ababneh; Sahar Alijanpour; Seyed Hassan Tonekaboni; Afshin Fayazi; Maria Urbaniak; Uxía Barba; Janet Hoenicka; Francesc Palau; Henry Houlden; Juan Darío Ortigoza-Escobar; Antonia Ribes; Carlos Santos-Ocaña; Millie Tyler; Patrick Gaffney; Christopher J Carroll; Frederic Tort; Klaas J Wierenga; Bryn D Webb; Rafael Artuch; Heidy Baide-Mairena; Roser Urreizti
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PIGC-related encephalopathy: Lessons learned from 18 new probandsPIGC相关的脑病:从18例新先证者中获得的经验教训
err2025-09-01
err0
PREAI
errBayat, Allan; Borroto, Maria Carla; Salian, Smrithi; Zaki, Maha S.; Benkerroum, Hind; Elbendary, Hasnaa M.; Nguyen, Thi Tuyet Mai; Sadek, Abdelrahim A.; Carli, Diana; Brusco, Alfredo; Ferrero, Giovanni Battista; Tartaglia, Marco; Hay, Eleanor; Krey, Ilona; A. Jamra, Rami; Bartolomaeus, Tobias; Knaus, Alexej; Gleeson, Joseph G.; Houlden, Henry; Dominik, Natalia; Jackson, Adam; Douzgou Houge, Sofia; Banka, Siddharth; Mohammadi-asl, Javad; Hajjari, Mohammadreza; Azizimalamiri, Reza; Nourbakhsh, Pardis; Neissi, Mostafa; Scardamaglia, Annarita; Li, Dianfan; Kinoshita, Taroh; Maroofian, Reza; Murakami, Yoshiko; Campeau, Philippe M.
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Case report of Pediatric DYT-HPCA: analysis of Ca2+ and K+ channel dynamics and experience with pallidal DBS儿科DYT-HPCA病例报告:Ca2+和K+通道动力学分析及苍白球DBS治疗经验
err2025-08-07
err0
PREAI
errLaia Nou-Fontanet; Jiraporn Ousingsawat; Majid Aziz; Reza Maroofian; Ehsan Ghayoor Karimiani; Anna Fernández-López; Santiago Candela-Cantó; Jordi Rumià; Ana Maria Dominguez; Rainer Schreiber; Karl Kunzelmann; Juan Dario Ortigoza-Escobar
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Recessive Loss of PI4K2A Function Causes a Developmental and Epileptic Dyskinetic Encephalopathy with Prominent Orolingual Dyskinesia隐性PI4K2A功能丧失导致一种伴有显著口舌运动障碍的发育性、癫痫性及运动障碍性脑病
err2025-08-07
err0
errOAAI
errReza Maroofian PhD; Juan Darío Ortigoza-Escobar MD, PhD; Pooja Rohilla PhD; Javeria Raza Alvi MD; Aziza M. Mushiba MD; Naif A.M. Almontashiri MD, PhD; Stephanie Efthymiou PhD; Tipu Sultan MD; Tamas Balla MD, PhD; Henry Houlden MD, PhD
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A programmed decline in ribosome levels governs human early neurodevelopment程序性核糖体水平下降调控人类早期神经发育
err2025-08-04
err0
errOAAI
errChunyang Ni; Yudong Wei; Barbara Vona; Dayea Park; Yulei Wei; Daniel A. Schmitz; Yi Ding; Masahiro Sakurai; Emily Ballard; Leijie Li; Yan Liu; Ashwani Kumar; Chao Xing; Shenlu Qin; Sangin Kim; Martina Foglizzo; Jianchao Zhao; Hyung-Goo Kim; Cumhur Ekmekci; Ehsan Ghayoor Karimiani; Shima Imannezhad; Fatemeh Eghbal; Reza Shervin Badv; Eva Maria Christina Schwaibold; Mohammadreza Dehghani; Mohammad Yahya Vahidi Mehrjardi; Zahra Metanat; Hosein Eslamiyeh; Ebtissal Khouj; Saleh Mohammed Nasser Alhajj; Aziza Chedrawi; Khushnooda Ramzan; Jamil A. Hashmi; Majed M. Alluqmani; Sulman Basit; Danai Veltra; Nikolaos M. Marinakis; Georgios Niotakis; Pelagia Vorgia; Christalena Sofocleous; Hane Lee; Won Chan Jeong; Muhammad Umair; Muhammad Bilal; César Augusto Pinheiro Ferreira Alves; Matthew Sieber; Michael Kruer; Henry Houlden; Fowzan S. Alkuraya; Elton Zeqiraj; Roger A. Greenberg; Can Cenik; Leqian Yu; Reza Maroofian; Jun Wu; Michael Buszczak
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