B. Leube

M. Pericak-Vance, M. Polymeropoulos, R. Nussbaum, 1998, DNA research : an international journal for rapid publication of reports on genes and genomes.

STK11 genotyping and cancer risk in Peutz-Jeghers syndrome

G. Möslein, B. Royer-Pokora, B. Leube, 2005, Journal of Medical Genetics.

Establishment of a Conditionally Immortalized Wilms Tumor Cell Line with a Homozygous WT1 Deletion within a Heterozygous 11p13 Deletion and UPD Limited to 11p15

J. Mora, C. de Torres, P. Jat, 2016, PloS one.

Synergistic mutations in SLC3A1 and SLC7A9 leading to heterogeneous cystinuria phenotypes: pitfalls in the diagnostic workup

T. Eggermann, A. Schlune, B. Leube, 2013, Pediatric Nephrology.

Mutations in CIZ1 cause adult onset primary cervical dystonia

D. Maraganore, R. Uitti, J. Perlmutter, 2012, Annals of neurology.

Cloning and tissue expression of two putative steroid membrane receptors.

E. Falkenstein, M. Wehling, B. Leube, 1998, Biological chemistry.

Clinical outcome and genotype in patients with hereditary multiple exostoses

M. Jäger, B. Royer-Pokora, B. Leube, 2007, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

SDHD mutation analysis in seven German patients with sporadic carotid body paraganglioma: one novel mutation, no Dutch founder mutation and further evidence that G12S is a polymorphism

B. Royer-Pokora, B. Leube, T. Goecke, 2003, Clinical genetics.

Ulna/height ratio as clinical parameter separating EXT1 from EXT2 families?

M. Jäger, B. Royer-Pokora, B. Leube, 2008, Genetic testing.

Mutations in CIZ1 are not a major cause for dystonia in Germany

T. Wächter, P. Bauer, T. Gasser, 2015, Movement disorders : official journal of the Movement Disorder Society.

Sporadic focal dystonia in Northwest Germany: Molecular basis on chromosome 18p

R. Benecke, K. Kessler, M. Knapp, 1997, Annals of neurology.

Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distribution.

R. Benecke, K. Kessler, G. Auburger, 1996, Human molecular genetics.

RNA biomarkers in prodromal PARK 4 and rapid eye movement sleep behavior disorder show role of complexin 1 loss for risk of Parkinson ' s disease

E. Schröck, W. Oertel, H. Steinmetz, 2018 .

Blood RNA biomarkers in prodromal PARK4 and rapid eye movement sleep behavior disorder show role of complexin 1 loss for risk of Parkinson's disease

E. Schröck, W. Oertel, H. Steinmetz, 2017, Disease Models & Mechanisms.

Questionable role of adult‐onset focal dystonia among sporadic dystonia patients

P. Goodfellow, S. Sawcer, A. Compston, 1998, Annals of neurology.

Evidence for DYT7 being a common cause of cervical dystonia (torticollis) in Central Europe.

K. Kessler, G. Auburger, B. Leube, 1997, American journal of medical genetics.

A phenotype map for 14q32.3 terminal deletions

A. Hoischen, R. Hennekam, S. Rudnik-Schöneborn, 2012, American journal of medical genetics. Part A.

Primary torsion dystonia: the search for genes is not over

D. Maraganore, A. Bentivoglio, A. Albanese, 1999, Journal of neurology, neurosurgery, and psychiatry.

Phenotypic variability of the DYT1 mutation in German dystonia patients

A. Ferbert, K. Kessler, F. Erbguth, 1999, Acta neurologica Scandinavica.

Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardation

R. Cohn, T. Voit, B. Leube, 1999, Neuromuscular Disorders.

Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family

R. Benecke, K. Kessler, G. Auburger, 1997, Movement disorders : official journal of the Movement Disorder Society.

Refined mapping of allele loss at chromosome 10q23‐26 in prostate cancer

T. Visakorpi, W. Schulz, R. Schäfer, 2002, The Prostate.

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.

P. Elliott, M. Jarvelin, C. Gieger, 2021 .