Rami Abou Jamra

Affiliations
  • Institute of Human Genetics, University of Leipzig, Leipzig, Germany.

Publications (37)

Novel EXOSC3 pathogenic variant results in a mild course of neurologic disease with cerebellum involvement.

European journal of medical genetics
Avec: Diana Le Duc , Susanne Horn , Rami Abou Jamra , Jörg Schaper , Dagmar Wieczorek , Silke Redler

Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Franziska Langhammer , Reza Maroofian , Rueda Badar , Anne Gregor , Michelle Rochman , Jeffrey B Ratliff , Marije Koopmans , Theresia Herget , Maja Hempel , Fanny Kortüm , Delphine Heron , Cyril Mignot , Boris Keren , Susan Brooks , Christina Botti , Bruria Ben-Zeev , Emanuela Argilli , Elliot H Sherr , Vykuntaraju K Gowda , Varunvenkat M Srinivasan , Somayeh Bakhtiari , Michael C Kruer , Mustafa A Salih , Alma Kuechler , Eric A Muller , Karli Blocker , Outi Kuismin , Kristen L Park , Aaina Kochhar , Kathleen Brown , Subhadra Ramanathan , Robin D Clark , Magdeldin Elgizouli , Gia Melikishvili , Nazhi Tabatadze , Zornitza Stark , Ghayda M Mirzaa , Jinfon Ong , Ute Grasshoff , Andrea Bevot , Lydia von Wintzingerode , Rami A Jamra , Yvonne Hennig , Paula Goldenberg , Chadi Al Alam , Majida Charif , Redouane Boulouiz , Mohammed Bellaoui , Rim Amrani , Fuad Al Mutairi , Abdullah M Tamim , Firdous Abdulwahab , Fowzan S Alkuraya , Ebtissal M Khouj , Javeria R Alvi , Tipu Sultan , Narges Hashemi , Ehsan G Karimiani , Farah Ashrafzadeh , Shima Imannezhad , Stephanie Efthymiou , Henry Houlden , Heinrich Sticht , Christiane Zweier

Re-evaluation and re-analysis of 152 research exomes five years after the initial report reveals clinically relevant changes in 18.

European journal of human genetics : EJHG
Avec: Tobias Bartolomaeus , Julia Hentschel , Rami Abou Jamra , Bernt Popp

De novo variants in SP9 cause a novel form of interneuronopathy characterized by intellectual disability, autism spectrum disorder, and epilepsy with variable expressivity.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Marine Tessarech , Gaëlle Friocourt , Florent Marguet , Maryline Lecointre , Morgane Le Mao , Rodrigo Muñoz Díaz , Cyril Mignot , Boris Keren , Bénédicte Héron , Charlotte De Bie , Koen Van Gassen , Didier Loisel , Benoit Delorme , Steffen Syrbe , Annick Klabunde-Cherwon , Rami Abou Jamra , Meret Wegler , Bert Callewaert , Annelies Dheedene , Merzouka Zidane-Marinnes , Agnès Guichet , Céline Bris , Patrick Van Bogaert , Florence Biquard , Guy Lenaers , Pascale Marcorelles , Claude Ferec , Bruno Gonzalez , Vincent Procaccio , Antonio Vitobello , Dominique Bonneau , Annie Laquerriere , Salim Khiati , Estelle Colin

The genetic landscape of intellectual disability and epilepsy in adults and the elderly: a systematic genetic work-up of 150 individuals.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Pia Zacher , Thomas Mayer , Frank Brandhoff , Tobias Bartolomaeus , Diana Le Duc , Martin Finzel , Anja Heinze , Susanne Horn , Chiara Klöckner , Gudrun Körber , Julia Hentschel , Malgorzata Kalita , Ilona Krey , Marina Nastainczyk-Wulf , Konrad Platzer , Johannes Rebstock , Bernt Popp , Mathias Stiller , Anne-Christin Teichmann , Rami Abou Jamra , Johannes R Lemke

Pontocerebellar hypoplasia due to bi-allelic variants in MINPP1.

European journal of human genetics : EJHG
Avec: Bart Appelhof , Matias Wagner , Julia Hoefele , Anja Heinze , Timo Roser , Margarete Koch-Hogrebe , Stefan D Roosendaal , Mohammadreza Dehghani , Mohammad Yahya Vahidi Mehrjardi , Erin Torti , Henry Houlden , Reza Maroofian , Farrah Rajabi , Heinrich Sticht , Frank Baas , Dagmar Wieczorek , Rami Abou Jamra

Germline AGO2 mutations impair RNA interference and human neurological development.

Nature communications
Avec: Davor Lessel , Daniela M Zeitler , Margot R F Reijnders , Andriy Kazantsev , Fatemeh Hassani Nia , Alexander Bartholomäus , Victoria Martens , Astrid Bruckmann , Veronika Graus , Allyn McConkie-Rosell , Marie McDonald , Bernarda Lozic , Ee-Shien Tan , Erica Gerkes , Jessika Johannsen , Jonas Denecke , Aida Telegrafi , Evelien Zonneveld-Huijssoon , Henny H Lemmink , Breana W M Cham , Tanja Kovacevic , Linda Ramsdell , Kimberly Foss , Diana Le Duc , Diana Mitter , Steffen Syrbe , Andreas Merkenschlager , Margje Sinnema , Bianca Panis , Joanna Lazier , Matthew Osmond , Taila Hartley , Jeremie Mortreux , Tiffany Busa , Chantal Missirian , Pankaj Prasun , Sabine Lüttgen , Ilaria Mannucci , Ivana Lessel , Claudia Schob , Stefan Kindler , John Pappas , Rachel Rabin , Marjolein Willemsen , Thatjana Gardeitchik , Katharina Löhner , Patrick Rump , Kerith-Rae Dias , Carey-Anne Evans , Peter Ian Andrews , Tony Roscioli , Han G Brunner , Chieko Chijiwa , M E Suzanne Lewis , Rami Abou Jamra , David A Dyment , Kym M Boycott , Alexander P A Stegmann , Christian Kubisch , Ene-Choo Tan , Ghayda M Mirzaa , Kirsty McWalter , Tjitske Kleefstra , Rolph Pfundt , Zoya Ignatova , Gunter Meister , Hans-Jürgen Kreienkamp

De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders.

American journal of human genetics
Avec: Marija Dulovic-Mahlow , Joanne Trinh , Krishna Kumar Kandaswamy , Geir Julius Braathen , Nataliya Di Donato , Elisa Rahikkala , Skadi Beblo , Martin Werber , Victor Krajka , Øyvind L Busk , Hauke Baumann , Nouriya Abbas Al-Sannaa , Frauke Hinrichs , Rabea Affan , Nir Navot , Mohammed A Al Balwi , Gabriela Oprea , Øystein L Holla , Maximilian E R Weiss , Rami A Jamra , Anne-Karin Kahlert , Shivendra Kishore , Kristian Tveten , Melissa Vos , Arndt Rolfs , Katja Lohmann

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases.

Research square
Avec: Tzung-Chien Hsieh , Hellen Lesmann , Alexander Hustinx , Shahida Moosa , Elaine Marchi , Maria Del Pilar Caro Martin , Ibrahim Abdelrazek , Jean Tori Pantel , Hannah Klinkhammer , Merle Ten Hagen , Meow-Keong Thong , Rifhan Azwani Binti Mazlan , Sok Kun Tae , Tom Kamphans , Wolfgang Meiswinkel , Jing-Mei Li , Behnam Javanmardi , Alexej Knaus , Annette Uwineza , Cordula Knopp , Tinatin Tkemaladze , Miriam Elbracht , Larissa Mattern , Rami Abou Jamra , Clara Velmans , Vincent Strehlow , Maureen Jacob , Angela Peron , Cristina Dias , Beatriz Nunes , Thainá Vilella , Isabel Pinheiro , Chong Kim , Maria Melaragno , Hannah Weiland , Sophia Kaptain , Karolina Chwiałkowska , Miroslaw Kwasniewski , Ramy Saad , Sarah Wiethoff , Himanshu Goel , Clara Tang , Anna Hau , Tahsin Stefan Barakat , Przemysław Panek , Amira Nabil , Julia Suh , Frederik Braun , Israel Gomy , Luisa Averdunk , Ekanem Ekure , Gaber Bergant , Borut Peterlin , Claudio Graziano , Nagwa Gaboon , Moisés Fiesco-Roa , Alessandro Spinelli , Nina-Maria Wilpert , Prasit Phowthongkum , Nergis Güzel , Tobias Haack , Rana Bitar , Andreas Tzschach , Agusti Rodriguez-Palmero , Theresa Brunet , Sabine Rudnik-Schöneborn , Silvina Contreras-Capetillo , Ava Oberlack , Carole Samango-Sprouse , Teresa Sadeghin , Margaret Olaya , Konrad Platzer , Artem Borovikov , Franziska Schnabel , Lara Heuft , Vera Herrmann , Renske Oegema , Nour Elkhateeb , Sheetal Kumar , Katalin Komlosi , Khoushoua Mohamed , Silvia Kalantari , Fabio Sirchia , Antonio Martinez-Monseny , Matthias Höller , Amal Mohamed , Amaia Lasa-Aranzasti , John Sayer , Nadja Ehmke , Magdalena Danyel , Henrike Sczakiel , Sarina Schwartzmann , Felix Boschann , Max Zhao , Ronja Adams , Lara Einicke , Denise Horn , Kee Seang Chew , Choy Chen Kam , Miray Karakoyun , Ben Pode-Shakked , Aviva Eliyahu , Rachel Rock , Teresa Carrion , Odelia Chorin , Yuri Zarate , Marcello Martinez , Mert Karakaya , Moon Ley Tung , Bharatendu Chandra , Aimé Lumaka , Marwan Shinawi , Patrick Blackburn , Tianyun Wang , Tim Niehues , Ping Hu , Rebekah Waikel , Suzanna Ledgister Hanchard , Gehad Elmakkawy , Sylvia Safwat , Frédéric Ebstein , Elke Krüger , Sébastien Küry , Stephane Bezieau , Annabelle Arlt , Felix Marbach , Dong Li , Lucie Dupuis , Roberto Mendoza-Londono , Sofia Douzgou Houge , Denisa Weis , Brian Chung , Christopher Mak , Nursel Elcioglu , Ayca Aykut , Peli Şimşek-Kiper , Nina Bögershausen , Bernd Wollnik , Heidi Beate Bentzen , Ingo Kurth , Christian Netzer , Aleksandra Jezela-Stanek , Koen Devriendt , Karen Gripp , Martin Mücke , Alain Verloes , Christian Schaaf , Christoffer Nellåker , Benjamin Solomon , Markus Nöthen , Ebtesam Abdalla , Gholson Lyon , Peter Krawitz , Hulya Kayserili , Louiza Toutouna , Axel Schmidt , Regina Roth , Dagmar Wieczorek , Eric Olinger

Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Elisabeth Bosch , Bernt Popp , Esther Güse , Cindy Skinner , Pleuntje J van der Sluijs , Isabelle Maystadt , Anna Maria Pinto , Alessandra Renieri , Lucia Pia Bruno , Stefania Granata , Carlo Marcelis , Özlem Baysal , Dewi Hartwich , Laura Holthöfer , Bertrand Isidor , Benjamin Cogne , Dagmar Wieczorek , Valeria Capra , Marcello Scala , Patrizia De Marco , Marzia Ognibene , Rami Abou Jamra , Konrad Platzer , Lauren B Carter , Outi Kuismin , Arie van Haeringen , Reza Maroofian , Irene Valenzuela , Ivon Cuscó , Julian A Martinez-Agosto , Ahna M Rabani , Heather C Mefford , Elaine M Pereira , Charlotte Close , Kwame Anyane-Yeboa , Mallory Wagner , Mark C Hannibal , Pia Zacher , Isabelle Thiffault , Gea Beunders , Muhammad Umair , Priya T Bhola , Erin McGinnis , John Millichap , Jiddeke M van de Kamp , Eloise J Prijoles , Amy Dobson , Amelle Shillington , Brett H Graham , Evan-Jacob Garcia , Maureen Kelly Galindo , Fabienne G Ropers , Esther A R Nibbeling , Gail Hubbard , Catherine Karimov , Guido Goj , Renee Bend , Julie Rath , Michelle M Morrow , Francisca Millan , Vincenzo Salpietro , Annalaura Torella , Vincenzo Nigro , Mitja Kurki , Roger E Stevenson , Gijs W E Santen , Markus Zweier , Philippe M Campeau , Mariasavina Severino , André Reis , Andrea Accogli , Georgia Vasileiou

Unveiling the crucial neuronal role of the proteasomal ATPase subunit gene

medRxiv : the preprint server for health sciences
Avec: Sébastien Küry , Janelle E Stanton , Geeske van Woerden , Tzung-Chien Hsieh , Cory Rosenfelt , Marie Pier Scott-Boyer , Victoria Most , Tianyun Wang , Jonas Johannes Papendorf , Charlotte de Konink , Wallid Deb , Virginie Vignard , Maja Studencka-Turski , Thomas Besnard , Anna Marta Hajdukowicz , Franziska Thiel , Sophie Möller , Laëtitia Florenceau , Silvestre Cuinat , Sylvain Marsac , Ingrid Wentzensen , Annabelle Tuttle , Cara Forster , Johanna Striesow , Richard Golnik , Damara Ortiz , Laura Jenkins , Jill A Rosenfeld , Alban Ziegler , Clara Houdayer , Dominique Bonneau , Erin Torti , Amber Begtrup , Kristin G Monaghan , Sureni V Mullegama , C M L Nienke Volker-Touw , Koen L I van Gassen , Renske Oegema , Mirjam de Pagter , Katharina Steindl , Anita Rauch , Ivan Ivanovski , Kimberly McDonald , Emily Boothe , Andrew Dauber , Janice Baker , Noelle Andrea V Fabie , Raphael A Bernier , Tychele N Turner , Siddharth Srivastava , Kira A Dies , Lindsay Swanson , Carrie Costin , Rebekah K Jobling , John Pappas , Rachel Rabin , Dmitriy Niyazov , Anne Chun-Hui Tsai , Karen Kovak , David B Beck , McV Malicdan , David R Adams , Lynne Wolfe , Rebecca D Ganetzky , Colleen Muraresku , Davit Babikyan , Zdeněk Sedláček , Miroslava Hančárová , Andrew T Timberlake , Hind Al Saif , Berkley Nestler , Kayla King , M J Hajianpour , Gregory Costain , D'Arcy Prendergast , Chumei Li , David Geneviève , Antonio Vitobello , Arthur Sorlin , Christophe Philippe , Tamar Harel , Ori Toker , Ataf Sabir , Derek Lim , Mark Hamilton , Lisa Bryson , Elaine Cleary , Sacha Weber , Trevor L Hoffman , Anna Maria Cueto-González , Eduardo Fidel Tizzano , David Gómez-Andrés , Marta Codina-Solà , Athina Ververi , Efterpi Pavlidou , Alexandros Lambropoulos , Kyriakos Garganis , Marlène Rio , Jonathan Levy , Sarah Jurgensmeyer , Anne M McRae , Mathieu Kent Lessard , Maria Daniela D'Agostino , Isabelle De Bie , Meret Wegler , Rami Abou Jamra , Susanne B Kamphausen , Viktoria Bothe , Larissa M Busch , Uwe Völker , Elke Hammer , Kristian Wende , Benjamin Cogné , Bertrand Isidor , Jens Meiler , Amélie Bosc-Rosati , Julien Marcoux , Marie-Pierre Bousquet , Jeremie Poschmann , Frédéric Laumonnier , Peter W Hildebrand , Evan E Eichler , Kirsty McWalter , Peter M Krawitz , Arnaud Droit , Ype Elgersma , Andreas M Grabrucker , Francois V Bolduc , Stéphane Bézieau , Frédéric Ebstein , Elke Krüger

Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Holly K Harris , Tojo Nakayama , Jenny Lai , Boxun Zhao , Nikoleta Argyrou , Cynthia S Gubbels , Aubrie Soucy , Casie A Genetti , Victoria Suslovitch , Lance H Rodan , George E Tiller , Gaetan Lesca , Karen W Gripp , Reza Asadollahi , Ada Hamosh , Carolyn D Applegate , Peter D Turnpenny , Marleen E H Simon , Catharina M L Volker-Touw , Koen L I van Gassen , Ellen van Binsbergen , Rolph Pfundt , Thatjana Gardeitchik , Bert B A de Vries , LaDonna L Immken , Catherine Buchanan , Marcia Willing , Tomi L Toler , Emily Fassi , Laura Baker , Fleur Vansenne , Xiadong Wang , Julian L Ambrus , Madeleine Fannemel , Jennifer E Posey , Emanuele Agolini , Antonio Novelli , Anita Rauch , Paranchai Boonsawat , Christina R Fagerberg , Martin J Larsen , Maria Kibaek , Audrey Labalme , Alice Poisson , Katelyn K Payne , Laurence E Walsh , Kimberly A Aldinger , Jorune Balciuniene , Cara Skraban , Christopher Gray , Jill Murrell , Caleb P Bupp , Giulia Pascolini , Paola Grammatico , Martin Broly , Sébastien Küry , Mathilde Nizon , Iqra Ghulam Rasool , Muhammad Yasir Zahoor , Cornelia Kraus , André Reis , Muhammad Iqbal , Kevin Uguen , Severine Audebert-Bellanger , Claude Ferec , Sylvia Redon , Janice Baker , Yunhong Wu , Guiseppe Zampino , Steffan Syrbe , Ines Brosse , Rami Abou Jamra , William B Dobyns , Lilian L Cohen , Anne Blomhoff , Cyril Mignot , Boris Keren , Thomas Courtin , Pankaj B Agrawal , Alan H Beggs , Timothy W Yu

PET/MRI Delivers Multimodal Brain Signature in Alzheimer's Disease with De Novo PSEN1 Mutation.

Current Alzheimer research
Avec: Gayane Aghakhanyan , Dorothee Saur , Michael Rullmann , Christopher M Weise , Matthias L Schroeter , Ken Marek , Rami Abou Jamra , Solveig Tiepolt , Maria Strauss , Cordula Scherlach , Karl-Titus Hoffmann , Osama Sabri , Joseph Classen , Henryk Barthel

Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Thomas A Ravenscroft , Jennifer B Phillips , Elizabeth Fieg , Sameer S Bajikar , Judy Peirce , Jeremy Wegner , Alia A Luna , Eric J Fox , Yi-Lin Yan , Jill A Rosenfeld , Jonathan Zirin , Oguz Kanca , Auteur inconnu , Paul J Benke , Eric S Cameron , Vincent Strehlow , Konrad Platzer , Rami Abou Jamra , Chiara Klöckner , Matthew Osmond , Thomas Licata , Samantha Rojas , David Dyment , Josephine S C Chong , Sharyn Lincoln , Joan M Stoler , John H Postlethwait , Michael F Wangler , Shinya Yamamoto , Joel Krier , Monte Westerfield , Hugo J Bellen

Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly.

Brain : a journal of neurology
Avec: Chiara Klöckner , J Pedro Fernández-Murray , Mahtab Tavasoli , Heinrich Sticht , Gisela Stoltenburg-Didinger , Leila Motlagh Scholle , Somayeh Bakhtiari , Michael C Kruer , Hossein Darvish , Saghar Ghasemi Firouzabadi , Alex Pagnozzi , Anju Shukla , Katta Mohan Girisha , Dhanya Lakshmi Narayanan , Parneet Kaur , Reza Maroofian , Maha S Zaki , Mahmoud M Noureldeen , Andreas Merkenschlager , Janina Gburek-Augustat , Elisa Cali , Selina Banu , Kamrun Nahar , Stephanie Efthymiou , Henry Houlden , Rami Abou Jamra , Jason Williams , Christopher R McMaster , Konrad Platzer

WARS1 and SARS1: Two tRNA synthetases implicated in autosomal recessive microcephaly.

Human mutation
Avec: Nina Bögershausen , Hannah E Krawczyk , Rami A Jamra , Sheng-Jia Lin , Gökhan Yigit , Irina Hüning , Anna M Polo , Barbara Vona , Kevin Huang , Julia Schmidt , Janine Altmüller , Johannes Luppe , Konrad Platzer , Beate B Dörgeloh , Andreas Busche , Saskia Biskup , Marisa I Mendes , Desiree E C Smith , Gajja S Salomons , Arne Zibat , Eva Bültmann , Peter Nürnberg , Malte Spielmann , Johannes R Lemke , Yun Li , Martin Zenker , Gaurav K Varshney , Hauke S Hillen , Christian P Kratz , Bernd Wollnik

ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networks.

Human molecular genetics
Avec: Maria W A Teunissen , Elly Lewerissa , Eline J H van Hugte , Shan Wang , Charlotte W Ockeloen , David A Koolen , Rolph Pfundt , Carlo L M Marcelis , Eva Brilstra , Jennifer L Howe , Stephen W Scherer , Xavier Le Guillou , Frédéric Bilan , Michelle Primiano , Jasmin Roohi , Amelie Piton , Anne de Saint Martin , Sarah Baer , Simone Seiffert , Konrad Platzer , Rami Abou Jamra , Steffen Syrbe , Jan H Doering , Shenela Lakhani , Srishti Nangia , Christian Gilissen , R Jeroen Vermeulen , Rob P W Rouhl , Han G Brunner , Marjolein H Willemsen , Nael Nadif Kasri

Frontiers in cell and developmental biology
Avec: Antje Kampmeier , Elsa Leitão , Ilaria Parenti , Jasmin Beygo , Christel Depienne , Nuria C Bramswig , Tzung-Chien Hsieh , Alexandra Afenjar , Stefanie Beck-Wödl , Ute Grasshoff , Tobias B Haack , Emilia K Bijlsma , Claudia Ruivenkamp , Eva Lausberg , Miriam Elbracht , Maria K Haanpää , Hannele Koillinen , Uwe Heinrich , Imma Rost , Rami Abou Jamra , Denny Popp , Margarete Koch-Hogrebe , Kevin Rostasy , Vanesa López-González , María José Sanchez-Soler , Catarina Macedo , Ariane Schmetz , Carmen Steinborn , Sabine Weidensee , Hellen Lesmann , Felix Marbach , Pilar Caro , Christian P Schaaf , Peter Krawitz , Dagmar Wieczorek , Frank J Kaiser , Alma Kuechler

Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Elisa Cali , Tania Quirin , Clarissa Rocca , Stephanie Efthymiou , Antonella Riva , Dana Marafi , Maha S Zaki , Mohnish Suri , Roberto Dominguez , Hasnaa M Elbendary , Shahryar Alavi , Mohamed S Abdel-Hamid , Heba Morsy , Frederic Tran Mau-Them , Mathilde Nizon , Pavel Tesner , Lukáš Ryba , Faisal Zafar , Nuzhat Rana , Nebal W Saadi , Zahra Firoozfar , Pinar Gencpinar , Bulent Unay , Canan Ustun , Ange-Line Bruel , Christine Coubes , Jennifer Stefanich , Ozlem Sezer , Emanuele Agolini , Antonio Novelli , Gessica Vasco , Donatella Lettori , Mathieu Milh , Laurent Villard , Shimriet Zeidler , Henry Opperman , Vincent Strehlow , Mahmoud Y Issa , Hebatallah El Khassab , Prem Chand , Shahnaz Ibrahim , Ali Nejad-Rashidi , Mohammad Miryounesi , Pegah Larki , Jennifer Morrison , Ingrid Cristian , Isabelle Thiffault , Nicole L Bertsch , Grace J Noh , John Pappas , Ellen Moran , Nikolaos M Marinakis , Joanne Traeger-Synodinos , Susan Hosseini , Mohammad Reza Abbaszadegan , Roseline Caumes , Lisenka E L M Vissers , Maedeh Neshatdoust , Mostafa Zohour Montazer , Elmostafa El Fahime , Christin Canavati , Lara Kamal , Moien Kanaan , Omar Askander , Victoria Voinova , Olga Levchenko , Shahzhad Haider , Sara S Halbach , Elias Rayana Maia , Salehi Mansoor , Jain Vivek , Sanjukta Tawde , Viveka Santhosh R Challa , Vykuntaraju K Gowda , Varunvenkat M Srinivasan , Lucas Alves Victor , Benito Pinero-Banos , Jennifer Hague , Heba Ahmed Ei-Awady , Adelia Maria de Miranda Henriques-Souza , Huma Arshad Cheema , Muhammad Nadeem Anjum , Sara Idkaidak , Firas Alqarajeh , Osama Atawneh , Hagar Mor-Shaked , Tamar Harel , Giovanni Zifarelli , Peter Bauer , Fernando Kok , Joao Paulo Kitajima , Fabiola Monteiro , Juliana Josahkian , Gaetan Lesca , Nicolas Chatron , Dorothe Ville , David Murphy , Jeffrey L Neul , Sureni V Mullegama , Amber Begtrup , Isabella Herman , Tadahiro Mitani , Jennifer E Posey , Chee Geap Tay , Iram Javed , Lucinda Carr , Farah Kanani , Fiona Beecroft , Lee Hane , Elsayed Abdelkreem , Milan Macek , Luciana Bispo , Marwa Abd Elmaksoud , Farzad Hashemi-Gorji , Davut Pehlivan , David J Amor , Rami Abou Jamra , Wendy K Chung , Eshan Karimiani Ghayoor , Philippe Campeau , Fowzan S Alkuraya , Alistair T Pagnamenta , Joseph Gleeson , James R Lupski , Pasquale Striano , Andres Moreno-De-Luca , Denis L J Lafontaine , Henry Houlden , Reza Maroofian

De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Ghayda M Mirzaa , Jessica X Chong , Amélie Piton , Bernt Popp , Kimberly Foss , Hui Guo , Ricardo Harripaul , Kun Xia , Joshua Scheck , Kimberly A Aldinger , Samin A Sajan , Sha Tang , Dominique Bonneau , Anita Beck , Janson White , Sonal Mahida , Jacqueline Harris , Constance Smith-Hicks , Juliane Hoyer , Christiane Zweier , André Reis , Christian T Thiel , Rami Abou Jamra , Natasha Zeid , Amy Yang , Laura S Farach , Laurence Walsh , Katelyn Payne , Luis Rohena , Milen Velinov , Alban Ziegler , Elise Schaefer , Vincent Gatinois , David Geneviève , Marleen E H Simon , Jennefer Kohler , Joshua Rotenberg , Patricia Wheeler , Austin Larson , Michelle E Ernst , Cigdem I Akman , Rachel Westman , Patricia Blanchet , Lori-Anne Schillaci , Catherine Vincent-Delorme , Karen W Gripp , Francesca Mattioli , Gwenaël Le Guyader , Bénédicte Gerard , Michèle Mathieu-Dramard , Gilles Morin , Roksana Sasanfar , Muhammad Ayub , Nasim Vasli , Sandra Yang , Rick Person , Kristin G Monaghan , Deborah A Nickerson , Ellen van Binsbergen , Gregory M Enns , Annika M Dries , Leah J Rowe , Anne C H Tsai , Shayna Svihovec , Jennifer Friedman , Zehra Agha , Raheel Qamar , Lance H Rodan , Julian Martinez-Agosto , Charlotte W Ockeloen , Marie Vincent , William James Sunderland , Jonathan A Bernstein , Auteur inconnu , Evan E Eichler , John B Vincent , Auteur inconnu , Michael J Bamshad

Value of renal gene panel diagnostics in adults waiting for kidney transplantation due to undetermined end-stage renal disease.

Kidney international
Avec: Isabel Ottlewski , Johannes Münch , Timo Wagner , Ria Schönauer , Anette Bachmann , Antje Weimann , Julia Hentschel , Tom H Lindner , Daniel Seehofer , Carsten Bergmann , Rami Abou Jamra , Jan Halbritter

Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Lance H Rodan , Rebecca C Spillmann , Harley T Kurata , Shawn M Lamothe , Jasmine Maghera , Rami Abou Jamra , Anna Alkelai , Stylianos E Antonarakis , Isis Atallah , Omer Bar-Yosef , Frédéric Bilan , Kathrine Bjorgo , Xavier Blanc , Patrick Van Bogaert , Yoav Bolkier , Lindsay C Burrage , Björn U Christ , Jorge L Granadillo , Patricia Dickson , Kirsten A Donald , Christèle Dubourg , Aviva Eliyahu , Lisa Emrick , Kendra Engleman , Michaela Veronika Gonfiantini , Jean-Marc Good , Judith Kalser , Chiara Kloeckner , Guus Lachmeijer , Marina Macchiaiolo , Francesco Nicita , Sylvie Odent , Emily O'Heir , Xilma Ortiz-Gonzalez , Marta Pacio-Miguez , María Palomares-Bralo , Loren Pena , Konrad Platzer , Mathieu Quinodoz , Emmanuelle Ranza , Jill A Rosenfeld , Eliane Roulet-Perez , Avni Santani , Fernando Santos-Simarro , Ben Pode-Shakked , Cara Skraban , Rachel Slaugh , Andrea Superti-Furga , Isabelle Thiffault , Richard H van Jaabrsveld , Marie Vincent , Hong-Gang Wang , Pia Zacher , Auteur inconnu , Eric Rush , Geoffrey S Pitt , Ping Yee Billie Au , Vandana Shashi

Molecular and Phenotypic Characterization of the

Neurology
Avec: Zeynep Gokce-Samar , Annalisa Vetro , Julitta De Bellescize , Tiziana Pisano , Laloe Monteiro , Noémie Penaud , Christian M Korff , Joel Fluss , Carla Marini , Elisabetta Cesaroni , Blanca Mercedes Alvarez , Damien Sanlaville , Nicolas Chatron , Alexis A Arzimanoglou , Audrey Labalme , Vishnu A Cuddapah , Sarah M Ruggiero , Francois Lecoquierre , Gael Nicolas , Guerrot Anne Marie , Axel Lebas , Herve O Testard , Katherine L Helbig , Anna Ruiz , Adeline Ngoh , Manju A Kurian , Kimberley Reid , Robert Spaull , Pascal Joset , Georgia Ramantani , Katharina Steindl , Martin Krenn , Lucia Gerstl , Silvia Vieker , Dana Craiu , Manuela Pendziwiat , Chad Haldeman-Englert , Ilya Kanivets , Irina Romanova , Deepa S Rajan , Jill A Rosenfeld , Margaret Au , Katheryn Grand , John M , Arnaud Isapof , Nathalie Villeneuve , Thomas Smol , Roseline Caumes , Pia Zacher , Sonja Neuser , Sigrid Tinschert , Konrad Platzer , Tobias Bartolomaeus , Ines Mohnke , Maximilian Radtke , Rami Abou Jamra , Ingo Helbig , Floortje E Jansen , Klaas Koop , Gabrielle Rudolf , Sebastien Küry , Julien Courchet , Renzo Guerrini , Gaetan Lesca

Bi-allelic loss-of-function variants in TMEM147 cause moderate to profound intellectual disability with facial dysmorphism and pseudo-Pelger-Huët anomaly.

American journal of human genetics
Avec: Quentin Thomas , Marialetizia Motta , Thierry Gautier , Maha S Zaki , Andrea Ciolfi , Julien Paccaud , François Girodon , Odile Boespflug-Tanguy , Thomas Besnard , Jennifer Kerkhof , Haley McConkey , Aymeric Masson , Anne-Sophie Denommé-Pichon , Benjamin Cogné , Eva Trochu , Virginie Vignard , Fatima El It , Lance H Rodan , Mohammad Ayman Alkhateeb , Rami Abou Jamra , Laurence Duplomb , Emilie Tisserant , Yannis Duffourd , Ange-Line Bruel , Adam Jackson , Siddharth Banka , Meriel McEntagart , Anand Saggar , Joseph G Gleeson , David Sievert , Hyunwoo Bae , Beom Hee Lee , Kisang Kwon , Go Hun Seo , Hane Lee , Anjum Saeed , Nadeem Anjum , Huma Cheema , Salem Alawbathani , Imran Khan , Jorge Pinto-Basto , Joyce Teoh , Jasmine Wong , Umar Bin Mohamad Sahari , Henry Houlden , Kristina Zhelcheska , Melanie Pannetier , Mona A Awad , Marion Lesieur-Sebellin , Giulia Barcia , Jeanne Amiel , Julian Delanne , Christophe Philippe , Laurence Faivre , Sylvie Odent , Aida Bertoli-Avella , Christel Thauvin , Bekim Sadikovic , Bruno Reversade , Reza Maroofian , Jérôme Govin , Marco Tartaglia , Antonio Vitobello

Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Heba Morsy , Mehdi Benkirane , Elisa Cali , Clarissa Rocca , Kristina Zhelcheska , Valentina Cipriani , Evangelia Galanaki , Reza Maroofian , Stephanie Efthymiou , David Murphy , Mary O'Driscoll , Mohnish Suri , Siddharth Banka , Jill Clayton-Smith , Thomas Wright , Melody Redman , Jennifer A Bassetti , Mathilde Nizon , Benjamin Cogne , Rami Abu Jamra , Tobias Bartolomaeus , Marion Heruth , Ilona Krey , Janina Gburek-Augustat , Dagmar Wieczorek , Felix Gattermann , Meriel Mcentagart , Alice Goldenberg , Lucie Guyant-Marechal , Hector Garcia-Moreno , Paola Giunti , Brigitte Chabrol , Severine Bacrot , Roger Buissonnière , Virginie Magry , Vykuntaraju K Gowda , Varunvenkat M Srinivasan , Béla Melegh , András Szabó , Katalin Sümegi , Mireille Cossée , Monica Ziff , Russell Butterfield , David Hunt , Georgina Bird-Lieberman , Michael Hanna , Michel Koenig , Michael Stankewich , Jana Vandrovcova , Henry Houlden , Auteur inconnu

Expanding the spectrum of EEF1D neurodevelopmental disorders: Biallelic variants in the guanine exchange domain.

Clinical genetics
Avec: Luisa Averdunk , Khalid Al-Thihli , Harald Surowy , Hermann-Josef Lüdecke , Matthias Drechsler , Gökhan Yigit , Lukasz Smorag , Bassam Al Hallak , Yun Li , Janine Altmüller , Tanja Guthoff , Michael Wallot , Peter Nürnberg , Bernd Wollnik , Rami Abou Jamra , Almundher Al-Maawali , Dagmar Wieczorek

Approach to Cohort-Wide Re-Analysis of Exome Data in 1000 Individuals with Neurodevelopmental Disorders.

Genes
Avec: Insa Halfmeyer , Tobias Bartolomaeus , Bernt Popp , Maximilian Radtke , Tobias Helms , Julia Hentschel , Denny Popp , Rami Abou Jamra

Hemophagocytic lymphohistiocytosis-like hyperinflammation due to a de novo mutation in DPP9.

The Journal of allergy and clinical immunology
Avec: Christine Wolf , Hannah Fischer , Jörn-Sven Kühl , Sarah Koss , Rami Abou Jamra , Sven Starke , Jurek Schultz , Stephan Ehl , Katrin Neumann , Catharina Schuetz , Robert Huber , Veit Hornung , Min Ae Lee-Kirsch

[Genetic Diagnostics in Everyday Clinical Practice in Child and Adolescent Psychiatry: Indications, Framework Conditions, Hurdles, and Proposed Solutions].

Zeitschrift fur Kinder- und Jugendpsychiatrie und Psychotherapie
Avec: Franziska Degenhardt , Eva Wohlleber , Rami Abou Jamra , Johannes Hebebrand

GestaltMatcher Database - A global reference for the facial phenotypic variability of rare human diseases.

medRxiv : the preprint server for health sciences
Avec: Hellen Lesmann , Alexander Hustinx , Shahida Moosa , Elaine Marchi , Pilar Caro , Ibrahim M Abdelrazek , Jean Tori Pantel , Hannah Klinkhammer , Merle Ten Hagen , Tom Kamphans , Wolfgang Meiswinkel , Jing-Mei Li , Behnam Javanmardi , Alexej Knaus , Annette Uwineza , Cordula Knopp , Tinatin Tkemaladze , Miriam Elbracht , Larissa Mattern , Rami Abou Jamra , Clara Velmans , Vincent Strehlow , Himanshu Goel , Beatriz Carvalho Nunes , Thainá Vilella , Isabel Furquim Pinheiro , Chong Ae Kim , Maria Isabel Melaragno , Tahsin Stefan Barakat , Amira Nabil , Julia Suh , Luisa Averdunk , Ekanem Ekure , Claudio Graziano , Prasit Phowthongkum , Nergis Güzel , Tobias B Haack , Theresa Brunet , Sabine Rudnik-Schöneborn , Konrad Platzer , Artem Borovikov , Franziska Schnabel , Lara Heuft , Vera Herrmann , Antonio F Martinez-Monseny , Matthias Höller , Khoshoua Alaaeldin , Aleksandra Jezela-Stanek , Amal Mohamed , Amaia Lasa-Aranzasti , John A Sayer , Ping Hu , Suzanna E Ledgister Hanchard , Gehad Elmakkawy , Sylvia Safwat , Frédéric Ebstein , Elke Krüger , Sébastien Küry , Annabelle Arlt , Felix Marbach , Christian Netzer , Sophia Kaptain , Hannah Weiland , Dong Li , Lucie Dupuis , Roberto Mendoza-Londono , Sofia Douzgou Houge , Denisa Weis , Brian Hon-Yin Chung , Christopher C Y Mak , Koen Devriendt , Karen W Gripp , Martin Mücke , Alain Verloes , Christian P Schaaf , Christoffer Nellåker , Benjamin D Solomon , Rebekah L Waikel , Markus M Nöthen , Ebtesam Abdalla , Gholson J Lyon , Peter M Krawitz , Tzung-Chien Hsieh

Evolutionary conserved networks of human height identify multiple Mendelian causes of short stature.

European journal of human genetics : EJHG
Avec: Nadine N Hauer , Bernt Popp , Leila Taher , Carina Vogl , Perundurai S Dhandapany , Christian Büttner , Steffen Uebe , Heinrich Sticht , Fulvia Ferrazzi , Arif B Ekici , Alessandro De Luca , Patrizia Klinger , Cornelia Kraus , Christiane Zweier , Antje Wiesener , Rami Abou Jamra , Erdmute Kunstmann , Anita Rauch , Dagmar Wieczorek , Anna-Marie Jung , Tilman R Rohrer , Martin Zenker , Helmuth-Guenther Doerr , André Reis , Christian T Thiel

Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration.

Brain : a journal of neurology
Avec: Christina R Fagerberg , Adrian Taylor , Felix Distelmaier , Henrik D Schrøder , Maria Kibæk , Dagmar Wieczorek , Mark Tarnopolsky , Lauren Brady , Martin J Larsen , Rami A Jamra , Annette Seibt , Eva Kildall Hejbøl , Else Gade , Ljubo Markovic , Dirk Klee , Peter Nagy , Nicholas Rouse , Prasoon Agarwal , Vernon W Dolinsky , Marica Bakovic

QRICH1 variants in Ververi-Brady syndrome-delineation of the genotypic and phenotypic spectrum.

Clinical genetics
Avec: Melanie Föhrenbach , Rami Abou Jamra , Arndt Borkhardt , Triantafyllia Brozou , Petra Muschke , Bernt Popp , Linda K Rey , Jörg Schaper , Harald Surowy , Martin Zenker , Christiane Zweier , Dagmar Wieczorek , Silke Redler

GABRA1-Related Disorders: From Genetic to Functional Pathways.

Annals of neurology
Avec: Elisa Musto , Vivian W Y Liao , Katrine M Johannesen , Christina D Fenger , Damien Lederer , Kavitha Kothur , Katrina Fisk , Bruce Bennetts , Pascal Vrielynck , Delphine Delaby , Berten Ceulemans , Sarah Weckhuysen , Peter Sparber , Arjan Bouman , Simone Ardern-Holmes , Christopher Troedson , Domenica I Battaglia , Himanshu Goel , Timothy Feyma , Somayeh Bakhtiari , Linda Tjoa , Martin Boxill , Nina Demina , Olga Shchagina , Elena Dadali , Michael Kruer , Gaetano Cantalupo , Ilaria Contaldo , Tilman Polster , Bertrand Isidor , Stefania M Bova , Walid Fazeli , Leen Wouters , Maria J Miranda , Francesca Darra , Elisa Pede , Diana Le Duc , Rami Abou Jamra , Sébastien Küry , Jacopo Proietti , Niamh McSweeney , Elly Brokamp , Peter Ian Andrews , Marie Gouray Garcia , Mary Chebib , Rikke S Møller , Philip K Ahring , Elena Gardella

Variant-specific pathophysiological mechanisms of

medRxiv : the preprint server for health sciences
Avec: Sissy Bassani , Jacqueline Chrast , Giovanna Ambrosini , Norine Voisin , Frédéric Schütz , Alfredo Brusco , Fabio Sirchia , Lydia Turban , Susanna Schubert , Rami Abou Jamra , Jan-Ulrich Schlump , Desiree DeMille , Pinar Bayrak-Toydemir , Gary Rex Nelson , Kristen Nicole Wong , Laura Duncan , Mackenzie Mosera , Christian Gilissen , Lisenka E L M Vissers , Rolph Pfundt , Rogier Kersseboom , Hilde Yttervik , Geir Åsmund Myge Hansen , Marie Falkenberg Smeland , Kameryn M Butler , Michael J Lyons , Claudia M B Carvalho , Chaofan Zhang , James R Lupski , Lorraine Potocki , Leticia Flores-Gallegos , Rodrigo Morales-Toquero , Florence Petit , Binnaz Yalcin , Annabelle Tuttle , Houda Zghal Elloumi , Lane Mccormick , Mary Kukolich , Oliver Klaas , Judit Horvath , Marcello Scala , Michele Iacomino , Francesca Operto , Federico Zara , Karin Writzl , Ales Maver , Maria K Haanpää , Pia Pohjola , Harri Arikka , Christian Iseli , Nicolas Guex , Alexandre Reymond

Lessons from two series by physicians and caregivers' self-reported data in DDX3X-related disorders.

Molecular genetics & genomic medicine
Avec: Valentin Ruault , Pauline Burger , Johanna Gradels-Hauguel , Nathalie Ruiz , Auteur inconnu , Rami Abou Jamra , Alexandra Afenjar , Yves Alembik , Jean-Luc Alessandri , Stéphanie Arpin , Giulia Barcia , Šárka Bendová , Ange-Line Bruel , Perrine Charles , Nicolas Chatron , Maya Chopra , Solène Conrad , Valérie Cormier Daire , Auriane Cospain , Christine Coubes , Juliette Coursimault , Andrée Delahaye-Duriez , Martine Doco , William Dufour , Benjamin Durand , Camille Engel , Laurence Faivre , Fanny Ferroul , Mélanie Fradin , Hélène Frenkiel , Carlo Fusco , Livia Garavelli , Aurore Garde , Bénédicte Gerard , David Germanaud , Louise Goujon , Aurélie Gouronc , Emmanuelle Ginglinger , Alice Goldenberg , Miroslava Hancarova , Markéta Havlovicová , Delphine Heron , Bertrand Isidor , Nolwenn Jean Marçais , Boris Keren , Margarete Koch-Hogrebe , Paul Kuentz , Victoria Lamure , Anne-Sophie Lebre , François Lecoquierre , Natacha Lehman , Gaetan Lesca , Stanislas Lyonnet , Delphine Martin , Cyril Mignot , Teresa M Neuhann , Gaël Nicolas , Mathilde Nizon , Florence Petit , Christophe Philippe , Amélie Piton , Marzia Pollazzon , Darina Prchalová , Audrey Putoux , Marlène Rio , Sophie Rondeau , Massimiliano Rossi , Quentin Sabbagh , Pascale Saugier-Veber , Ariane Schmetz , Julie Steffann , Christel Thauvin-Robinet , Annick Toutain , Frederic Tran Mau Them , Gabriele Trimarchi , Marie Vincent , Markéta Vlčková , Dagmar Wieczorek , Marjolaine Willems , Kevin Yauy , Michaela Zelinová , Alban Ziegler , Auteur inconnu , Boris Chaumette , Bekim Sadikovic , Jean-Louis Mandel , David Geneviève

CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.

European journal of human genetics : EJHG
Avec: Henry Oppermann , Elia Marcos-Grañeda , Linnea A Weiss , Christina A Gurnett , Anne Marie Jelsig , Susanne H Vineke , Bertrand Isidor , Sandra Mercier , Kari Magnussen , Pia Zacher , Mona Hashim , Alistair T Pagnamenta , Simone Race , Siddharth Srivastava , Zoë Frazier , Robert Maiwald , Matthias Pergande , Donatella Milani , Martina Rinelli , Jonathan Levy , Ilona Krey , Paolo Fontana , Fortunato Lonardo , Stephanie Riley , Jasmine Kretzer , Julia Rankin , Linda M Reis , Elena V Semina , Miriam S Reuter , Stephen W Scherer , Maria Iascone , Denisa Weis , Christina R Fagerberg , Charlotte Brasch-Andersen , Lars Kjaersgaard Hansen , Alma Kuechler , Nathan Noble , Alice Gardham , Jessica Tenney , Geetanjali Rathore , Stefanie Beck-Woedl , Tobias B Haack , Despoina C Pavlidou , Isis Atallah , Julia Vodopiutz , Andreas R Janecke , Tzung-Chien Hsieh , Hellen Lesmann , Hannah Klinkhammer , Peter M Krawitz , Johannes R Lemke , Rami Abou Jamra , Marta Nieto , Zeynep Tümer , Konrad Platzer

Réseau de co-auteurs

Dagmar Wieczorek 11 collaborations
Konrad Platzer 11 collaborations
Reza Maroofian 7 collaborations
Bernt Popp 7 collaborations
None None 7 collaborations
Henry Houlden 6 collaborations
Tobias Bartolomaeus 5 collaborations
Pia Zacher 5 collaborations
Tzung-Chien Hsieh 5 collaborations
Sébastien Küry 5 collaborations
Bertrand Isidor 5 collaborations
Diana Le Duc 4 collaborations
Cyril Mignot 4 collaborations
Boris Keren 4 collaborations
Rami A Jamra 4 collaborations
Stephanie Efthymiou 4 collaborations
Heinrich Sticht 4 collaborations
Christiane Zweier 4 collaborations
Julia Hentschel 4 collaborations
Rolph Pfundt 4 collaborations
Hellen Lesmann 4 collaborations
Vincent Strehlow 4 collaborations
André Reis 4 collaborations
Jill A Rosenfeld 4 collaborations
Lance H Rodan 4 collaborations
Gaetan Lesca 4 collaborations
Mathilde Nizon 4 collaborations
Vykuntaraju K Gowda 3 collaborations
Varunvenkat M Srinivasan 3 collaborations
Somayeh Bakhtiari 3 collaborations
Alma Kuechler 3 collaborations
Ghayda M Mirzaa 3 collaborations
Steffen Syrbe 3 collaborations
Antonio Vitobello 3 collaborations
Dominique Bonneau 3 collaborations
Chiara Klöckner 3 collaborations
Ilona Krey 3 collaborations
Johannes R Lemke 3 collaborations
Margarete Koch-Hogrebe 3 collaborations
John Pappas 3 collaborations
Hannah Klinkhammer 3 collaborations
Miriam Elbracht 3 collaborations
Himanshu Goel 3 collaborations
Luisa Averdunk 3 collaborations
Frédéric Ebstein 3 collaborations
Elke Krüger 3 collaborations
Felix Marbach 3 collaborations
Denisa Weis 3 collaborations
Bernd Wollnik 3 collaborations
Isabelle Thiffault 3 collaborations
Alban Ziegler 3 collaborations
Anita Rauch 3 collaborations
David Geneviève 3 collaborations
Christophe Philippe 3 collaborations
Peter M Krawitz 3 collaborations
Karen W Gripp 3 collaborations
Christina R Fagerberg 3 collaborations
Maha S Zaki 3 collaborations
Elisa Cali 3 collaborations
Martin Zenker 3 collaborations
Tobias B Haack 3 collaborations
Ange-Line Bruel 3 collaborations
Nicolas Chatron 3 collaborations
Marie Vincent 3 collaborations
Susanne Horn 2 collaborations
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Silke Redler 2 collaborations
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Outi Kuismin 2 collaborations
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Claude Ferec 2 collaborations
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Matthew Osmond 2 collaborations
Rachel Rabin 2 collaborations
Thatjana Gardeitchik 2 collaborations
Peter Ian Andrews 2 collaborations
Han G Brunner 2 collaborations
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Alexander Hustinx 2 collaborations
Shahida Moosa 2 collaborations
Elaine Marchi 2 collaborations
Jean Tori Pantel 2 collaborations
Merle Ten Hagen 2 collaborations
Tom Kamphans 2 collaborations
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Behnam Javanmardi 2 collaborations
Alexej Knaus 2 collaborations
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Tinatin Tkemaladze 2 collaborations
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Clara Velmans 2 collaborations
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Hannah Weiland 2 collaborations
Sophia Kaptain 2 collaborations
Tahsin Stefan Barakat 2 collaborations
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Julia Suh 2 collaborations
Ekanem Ekure 2 collaborations
Claudio Graziano 2 collaborations
Prasit Phowthongkum 2 collaborations
Nergis Güzel 2 collaborations
Theresa Brunet 2 collaborations
Sabine Rudnik-Schöneborn 2 collaborations
Artem Borovikov 2 collaborations
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Lara Heuft 2 collaborations
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Renske Oegema 2 collaborations
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Amal Mohamed 2 collaborations
Amaia Lasa-Aranzasti 2 collaborations
Ben Pode-Shakked 2 collaborations
Aviva Eliyahu 2 collaborations
Tianyun Wang 2 collaborations
Ping Hu 2 collaborations
Gehad Elmakkawy 2 collaborations
Sylvia Safwat 2 collaborations
Annabelle Arlt 2 collaborations
Dong Li 2 collaborations
Lucie Dupuis 2 collaborations
Roberto Mendoza-Londono 2 collaborations
Sofia Douzgou Houge 2 collaborations
Nina Bögershausen 2 collaborations
Christian Netzer 2 collaborations
Aleksandra Jezela-Stanek 2 collaborations
Koen Devriendt 2 collaborations
Martin Mücke 2 collaborations
Alain Verloes 2 collaborations
Christoffer Nellåker 2 collaborations
Ebtesam Abdalla 2 collaborations
Peter Krawitz 2 collaborations
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Marcello Scala 2 collaborations
Virginie Vignard 2 collaborations
Thomas Besnard 2 collaborations
Annabelle Tuttle 2 collaborations
Amber Begtrup 2 collaborations
Kristin G Monaghan 2 collaborations
Sureni V Mullegama 2 collaborations
Koen L I van Gassen 2 collaborations
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Janice Baker 2 collaborations
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Tamar Harel 2 collaborations
Marlène Rio 2 collaborations
Jonathan Levy 2 collaborations
Benjamin Cogné 2 collaborations
Evan E Eichler 2 collaborations
Marleen E H Simon 2 collaborations
Ellen van Binsbergen 2 collaborations
Jennifer E Posey 2 collaborations
Emanuele Agolini 2 collaborations
Antonio Novelli 2 collaborations
Martin J Larsen 2 collaborations
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Kimberly A Aldinger 2 collaborations
Cara Skraban 2 collaborations
Cornelia Kraus 2 collaborations
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Peter Nürnberg 2 collaborations
Yun Li 2 collaborations
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Stephen W Scherer 2 collaborations
Frédéric Bilan 2 collaborations
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Alexandra Afenjar 2 collaborations
Maria K Haanpää 2 collaborations
Denny Popp 2 collaborations
Ariane Schmetz 2 collaborations
Pilar Caro 2 collaborations
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Clarissa Rocca 2 collaborations
Mohnish Suri 2 collaborations
Heba Morsy 2 collaborations
Christine Coubes 2 collaborations
Roseline Caumes 2 collaborations
Lisenka E L M Vissers 2 collaborations
David Murphy 2 collaborations
Alistair T Pagnamenta 2 collaborations
James R Lupski 2 collaborations
Amélie Piton 2 collaborations
Christian T Thiel 2 collaborations
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Isis Atallah 2 collaborations
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