Philippe Debeer - Publications, H-index & Citations

Philippe Debeer

university hospital leuven

29H指数

150论文数

2.6K被引数

收录论文 13

发表时间

Management of a first time anterior shoulder dislocation: the decision-making process of a surgeon 初次前肩关节脱位的处理：外科医生的决策过程

Journal of Shoulder and Elbow Surgery

IF2.9

2025-09-02

PREAI

Liselore Quintens; Filip Verhaegen; Philippe Debeer

Covariation between rotator cuff muscle quality and shoulder morphometric bony features in B-glenoids: a statistical modeling approach B型盂窝中旋转袖肌肉质量与肩部骨骼形态测量特征之间的共变关系：一种统计建模方法

Biomechanics and Modeling in Mechanobiology

IF2.7

2025-06-17

PREAI

Nazanin Daneshvarhashjin; Philippe Debeer; Harold Matthews; Peter Claes; Filip Verhaegen; Lennart Scheys

Effectiveness of Botulinum Toxin A for Persistent Upper Limb Pain After Breast Cancer Treatment: A Double-Blinded Randomized Controlled Trial

ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION

IF3.7

2018-07-01

OAAI

De Groef, An; Devoogdt, Nele; Van Kampen, Marijke; Nevelsteen, Ines; Smeets, Ann; Neven, Patrick; Geraerts, Inge; Dams, Lore; Van der Gucht, Ellen; Debeer, Philippe

An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning†

HUMAN MOLECULAR GENETICS

IF3.2

2012-02-27

OAAI

Brison, Nathalie; Debeer, Philippe; Fantini, Sebastian; Oley, Christine; Zappavigna, Vincenzo; Luyten, Frank P.; Tylzanowski, Przemko

Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani-Lenz-like non-syndromic oligosyndactyly

JOURNAL OF MEDICAL GENETICS

IF3.7

2010-07-07

OAAI

Dimitrov, Boyan Ivanov; Voet, Thierry; De Smet, Luc; Vermeesch, Joris Robert; Devriendt, Koen; Fryns, Jean-Pierre; Debeer, Philippe

A G220V substitution within the N-terminal transcription regulating domain of HOXD13 causes a variant synpolydactyly phenotype

HUMAN MOLECULAR GENETICS

IF3.2

2008-12-05

OAAI

Fantini, Sebastian; Vaccari, Giulia; Brison, Nathalie; Debeer, Philippe; Tylzanowski, Przemko; Zappavigna, Vincenzo

A homozygous mutation in the lamin A/C gene associated with a novel syndrome of arthropathy, tendinous calcinosis, and progeroid features

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

IF5.1

2006-02-01

OAAI

Van Esch, H; Agarwal, AK; Debeer, P; Fryns, JP; Garg, A

Early recognition of basal cell naevus syndrome

EUROPEAN JOURNAL OF PEDIATRICS

IF2.6

2004-12-10

PREAI

Debeer, P; Devriendt, K

Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis

NATURE GENETICS

IF31.8

2004-10-17

369

OAAI

Hellemans, J; Preobrazhenska, O; Willaert, A; Debeer, P; Verdonk, PCM; Costa, T; Janssens, K; Menten, B; Van Roy, N; Vermeulen, SJT; Savarirayan, R; Van Hul, W; Vanhoenacker, F; Huylebroeck, D; De Paepe, A; Naeyaert, JM; Vandesompele, J; Speleman, F; Verschueren, K; Coucke, PJ; Mortier, GR

PA26 is a candidate gene for heterotaxia in humans:: identification of a novel PA26-related gene family in human and mouse

HUMAN GENETICS

IF3.6

2003-02-27

116

PREAI

Peeters, H; Debeer, P; Bairoch, A; Wilquet, V; Huysmans, C; Parthoens, E; Fryns, JP; Gewillig, M; Nakamura, Y; Niikawa, N; Van de Ven, W; Devriendt, K

Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13

JOURNAL OF MEDICAL GENETICS

IF3.7

2002-11-01

OAAI

Debeer, P; Bacchelli, C; Scambler, PJ; De Smet, L; Fryns, JP; Goodman, FR

The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly

JOURNAL OF MEDICAL GENETICS

IF3.7

2002-02-01

OAAI

Debeer, P; Schoenmakers, EFPM; Twal, WO; Argraves, WS; De Smet, L; Fryns, JP; Van de Ven, WJM