A. Heimbach

发表

The severity of human peri‐implantitis lesions correlates with the level of submucosal microbial dysbiosis

P. Papapanou, P. Hoffmann, F. Schwarz, 2018, Journal of clinical periodontology.

Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum

M. Rietschel, M. Nöthen, R. Spanagel, 2022, Translational Psychiatry.

F8 Inversions at Xq28 Causing Hemophilia A Are Associated With Specific Methylation Changes: Implication for Molecular Epigenetic Diagnosis

M. Jamil, Amit Sharma, J. Oldenburg, 2019, Front. Genet..

CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT).

P. Winyard, D. Fischer, D. Haffner, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores

A. Hoischen, T. Becker, M. Nothnagel, 2022, Molecular genetics & genomic medicine.

I. Horenko, S. Gerber, M. Müller, 2022, Cells.

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

Jan Gründemann, C. Woods, A. Mubaidin, 2006, Nature Genetics.

Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum

M. Rietschel, R. Spanagel, S. Heilmann-Heimbach, 2021, Translational Psychiatry.

Early IFN-α signatures and persistent dysfunction are distinguishing features of NK cells in severe COVID-19

Konrad U. Förstner, Philipp H. Schiffer, Joseph M. Johnson, 2021, Immunity.

Disease severity-specific neutrophil signatures in blood transcriptomes stratify COVID-19 patients

Konrad U. Förstner, Philipp H. Schiffer, P. Bork, 2020, Genome Medicine.

Deleterious somatic variants in 473 consecutive individuals with ovarian cancer: results of the observational AGO-TR1 study (NCT02222883)

A. Reuss, H. Gevensleben, D. Dietrich, 2019, Journal of Medical Genetics.

Sensitivity and specificity of loss of heterozygosity analysis for the classification of rare germline variants in BRCA1/2: results of the observational AGO-TR1 study (NCT02222883)

A. Reuss, H. Gevensleben, D. Dietrich, 2020, Journal of Medical Genetics.

Compound heterozygous SZT2 mutations in two siblings with early-onset epilepsy, intellectual disability and macrocephaly

F. S. Domingues, P. Pramstaller, P. Hoffmann, 2019, Seizure.

Characterization of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection Clusters Based on Integrated Genomic Surveillance, Outbreak Analysis and Contact Tracing in an Urban Setting

Konrad U. Förstner, Philipp H. Schiffer, Jonathan L. Schmid-Burgk, 2021, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Prevalence of deleterious germline variants in risk genes including BRCA1/2 in consecutive ovarian cancer patients (AGO-TR-1)

A. Reuss, H. Gevensleben, D. Dietrich, 2017, PloS one.

Pathogenic effects of novel mutations in the P‐type ATPase ATP13A2 (PARK9) causing Kufor‐Rakeb syndrome, a form of early‐onset parkinsonism

D. Krainc, A. Mackay-Sim, A. Cooper, 2011, Human mutation.

Incidence of germline mutations in risk genes including BRCA1/2 in consecutive ovarian cancer (OC) patients (AGO TR-1)

A. Reuss, R. Schmutzler, F. Marmé, 2016 .

CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT).

P. Winyard, D. Fischer, D. Haffner, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.