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Papers共 75 篇Author StatisticsCo-AuthorSimilar Experts

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GestaltMatcher Database - A Global Reference for Facial Phenotypic Variability in Rare Human Diseases
Hellen Lesmann,Alexander Hustinx,Shahida Moosa,Hannah Klinkhammer,Elaine Marchi,Pilar Caro,Ibrahim M Abdelrazek,Jean Tori Pantel, 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 Carvalho Nunes, Thainá Vilella, Isabel Furquim Pinheiro,Chong Ae Kim,Maria Isabel 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 Mauro Spinelli, Nina-Maria Wilpert,Prasit Phowthongkum,Nergis Güzel,Tobias B Haack, Rana Bitar, Andreas Tzschach, Agusti Rodriguez-Palmero,Theresa Brunet,Sabine Rudnik-Schöneborn, Silvina Noemi 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 F Martinez-Monseny, Matthias Höller, Louiza Toutouna, Amal Mohamed,Amaia Lasa-Aranzasti,John A Sayer,Nadja Ehmke,Magdalena Danyel,Henrike Sczakiel,Sarina Schwartzmann,Felix Boschann,Max Zhao,Ronja Adam, Lara Einicke, Denise Horn,Kee Seang Chew, Choy Chen Kam, Miray Karakoyun,Ben Pode-Shakked,Aviva Eliyahu,Rachel Rock, Teresa Carrion,Odelia Chorin,Yuri A Zarate, Marcelo Martinez Conti,Mert Karakaya,Moon Ley Tung,Bharatendu Chandra,Arjan Bouman,Aime Lumaka,Naveed Wasif,Marwan Shinawi,Patrick R Blackburn,Tianyun Wang, Tim Niehues,Axel Schmidt, Regina Rita Roth,Dagmar Wieczorek,Ping Hu,Rebekah L Waikel,Suzanna E Ledgister Hanchard,Gehad Elmakkawy,Sylvia Safwat,Frédéric Ebstein,Elke Krüger,Sébastien Küry,Stéphane Bézieau,Annabelle Arlt,Eric Olinger,Felix Marbach, Dong Li,Lucie Dupuis,Roberto Mendoza-Londono,Sofia Douzgou Houge,Denisa Weis,Brian Hon-Yin Chung,Christopher C Y Mak,Hülya Kayserili,Nursel Elcioglu,Ayca Aykut, Peli Özlem Şimşek-Kiper,Nina Bögershausen,Bernd Wollnik,Heidi Beate Bentzen, Ingo Kurth,Christian Netzer,Aleksandra Jezela-Stanek,Koen Devriendt,Karen W Gripp,Martin Mücke,Alain Verloes,Christian P Schaaf,Christoffer Nellåker,Benjamin D Solomon,Markus M Nöthen,Ebtesam Abdalla,Gholson J Lyon,Peter M Krawitz,Tzung-Chien Hsieh
medRxiv the preprint server for health sciences (2024)
Cited3Views0WOSBibtex
3
0
Deciphering Developmental Disorders in Africa (Ddd-Africa) -the First ∼100 Cases from South Africa
Krause, Barry Shingwenyana,Nadia Carstens,Phelelani Mpangase, Mhlekazi Molatoli,Patracia Nevondwe, Nadja Louw,Aime Lumaka, Prosper Lukusa,Koenraad Devriendt,Zane Lombard
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 471-472
Cited0Views0Bibtex
0
0
Pushing the Boundaries of Rare Disease Diagnostics with the Help of the First Undiagnosed Hackathon
Angelica Maria Delgado-Vega,Helene Cederroth,Fulya Taylan,Katja Ekholm,Marlene Ek,Håkan Thonberg,Anders Jemt,Daniel Nilsson,Jesper Eisfeldt,Kristine Bilgrav Saether,Ida Höijer,Ozlem Akgun-Dogan, Yui Asano,Tahsin Stefan Barakat,Dominyka Batkovskyte,Gareth Baynam,Olaf Bodamer,Wanna Chetruengchai, Pádraic Corcoran,Madeline Couse,Daniel Danis,German Demidov, Eisuke Dohi, Mattias Erhardsson, Luis Fernandez-Luna,Toyofumi Fujiwara, Neha Garg, Roberto Giugliani,Claudia Gonzaga-Jauregui,Giedre Grigelioniene,Tudor Groza,Cecilia Gunnarsson,Anna Hammarsjö, Charles Kumi Hammond,Özden Hatirnaz Ng, Sirisha Hesketh,Dineshani Hettiarachchi,Maria Johansson Soller, Umn Ahmed Kirmani, Martin Kjellberg,Malin Kvarnung,Oleg Kvlividze,Kristina Lagerstedt-Robinson,Paul Lasko,Timo Lassmann, Lynette Y S Lau,Steven Laurie,Weng Khong Lim,Zhandong Liu,Mariya Lysenkova Wiklander,Prince Makay, Alassane Baneye Maiga,Carolina Maya-González,M Stephen Meyn, Ramprasad Neethiraj, Vincenzo Nigro, Felix Nordgren,Jessica Nordlund, Sara Orrsjö,Jesper Ottosson,Ugur Ozbek,Özkan Özdemir,Clyde Partin,David A Pearce, Raquel Peck, Annie Pedersen,Maria Pettersson,Monnat Pongpanich,Manuel Posada de la Paz,Arun Ramani, Juan Andres Romero,Vanessa I Romero,Richard Rosenquist, Aung Min Saw, Matthew Spencer,Eva-Lena Stattin,Chalurmpon Srichomthong,Isabel Tapia-Paez,Domenica Taruscio,Julie P Taylor,Tinatin Tkemaladze, Ian Tully,Zeynep Tümer, Wendy A G van Zelst-Stams,Alain Verloes, Emma Västerviga,Sailan Wang, Rachel Yang,Shinya Yamamoto,Vicente A Yépez, Qing Zhang,Vorasuk Shotelersuk,Samuel Agyei Wiafe,Yasemin Alanay,Lorenzo D Botto,Salman Kirmani,Aimé Lumaka,Elizabeth Emma Palmer,Ratna Dua Puri,Valtteri Wirta,Anna Lindstrand,Orion J Buske, Mikk Cederroth,Ann Nordgren
Nature geneticsno. 11 (2024): 2287-2294
Cited0Views0WOSNATUREBibtex
0
0
My Bantu Vision of Genomic Medicine in Africa
Aimé Lumaka
Nature Geneticspp.1-3, (2023)
Cited0Views0WOSNATUREBibtex
0
0
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Author Statistics

#Papers: 76

#Citation: 396

H-Index: 12

G-Index: 18

Sociability: 6

Diversity: 2

Activity: 22

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