Search Results - "Heilmann, S."

Design of a migration assay for human gingival fibroblasts on biodegradable magnesium surfaces by Amberg, R., Elad, A., Rothamel, D., Fienitz, T., Szakacs, G., Heilmann, S., Witte, F.

“…[Display omitted] A novel regenerative approach to Guided Bone Regeneration (GBR) in dental surgery is based on the development of biodegradable and volume…”
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Common variants in DLG1 locus are associated with non‐syndromic cleft lip with or without cleft palate by Mostowska, A., Gaczkowska, A., Żukowski, K., Ludwig, K.U., Hozyasz, K.K., Wójcicki, P., Mangold, E., Böhmer, A.C., Heilmann‐Heimbach, S., Knapp, M., Zadurska, M., Biedziak, B., Budner, M., Lasota, A., Daktera‐Micker, A., Jagodziński, P.P.

“…Non‐syndromic cleft lip with or without cleft palate (nsCL/P) is a common craniofacial anomaly with a complex and heterogeneous aetiology. Knowledge regarding…”
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Genome-wide significant risk factors for Alzheimer’s disease: role in progression to dementia due to Alzheimer's disease among subjects with mild cognitive impairment by Lacour, A, Espinosa, A, Louwersheimer, E, Heilmann, S, Hernández, I, Wolfsgruber, S, Fernández, V, Wagner, H, Rosende-Roca, M, Mauleón, A, Moreno-Grau, S, Vargas, L, Pijnenburg, Y A L, Koene, T, Rodríguez-Gómez, O, Ortega, G, Ruiz, S, Holstege, H, Sotolongo-Grau, O, Kornhuber, J, Peters, O, Frölich, L, Hüll, M, Rüther, E, Wiltfang, J, Scherer, M, Riedel-Heller, S, Alegret, M, Nöthen, M M, Scheltens, P, Wagner, M, Tárraga, L, Jessen, F, Boada, M, Maier, W, van der Flier, W M, Becker, T, Ramirez, A, Ruiz, A

“…Few data are available concerning the role of risk markers for Alzheimer’s disease (AD) in progression to AD dementia among subjects with mild cognitive…”
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Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19 by Henne, S. K., Hochfeld, L. M., Maj, C., Nöthen, M. M., Heilmann‐Heimbach, S.

“…Background Male androgenetic alopecia (AGA) has been implicated as a putative risk factor in severe COVID‐19 based on high incidences of advanced AGA in male…”
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Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk-Locus Xq28,distal by Claus, I, Sivalingam, S, Koller, A C, Weiß, A, Mathey, C M, Sindermann, L, Klein, D, Henschel, L, Ludwig, K U, Hoffmann, P, Heimbach, A, Heilmann-Heimbach, S, Vedder, H, Kammerer-Ciernioch, J, Stürmer, T, Streit, F, Maaser-Hecker, A, Nenadić, I, Baune, B T, Hartmann, A M, Konte, B, Giegling, I, Heilbronner, U, Wagner, M, Philipsen, A, Schmidt, B, Rujescu, D, Buness, A, Schulze, T G, Rietschel, M, Forstner, A J, Nöthen, M M, Degenhardt, F

“…Duplications of the Xq28,distal locus have been described in male and female patients with schizophrenia (SCZ) or intellectual disability. The Xq28,distal…”
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Follow-up of loci from the International Genomics of Alzheimer’s Disease Project identifies TRIP4 as a novel susceptibility gene by Ruiz, A, Heilmann, S, Becker, T, Hernández, I, Wagner, H, Thelen, M, Mauleón, A, Rosende-Roca, M, Bellenguez, C, Bis, J C, Harold, D, Gerrish, A, Sims, R, Sotolongo-Grau, O, Espinosa, A, Alegret, M, Arrieta, J L, Lacour, A, Leber, M, Becker, J, Lafuente, A, Ruiz, S, Vargas, L, Rodríguez, O, Ortega, G, Dominguez, M-A, Mayeux, R, Haines, J L, Pericak-Vance, M A, Farrer, L A, Schellenberg, G D, Chouraki, V, Launer, L J, van Duijn, C, Seshadri, S, Antúnez, C, Breteler, M M, Serrano-Ríos, M, Jessen, F, Tárraga, L, Nöthen, M M, Maier, W, Boada, M, Ramírez, A

“…To follow-up loci discovered by the International Genomics of Alzheimer’s Disease Project, we attempted independent replication of 19 single nucleotide…”
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Evidence for a polygenic contribution to androgenetic alopecia by Heilmann, S., Brockschmidt, F.F., Hillmer, A.M., Hanneken, S., Eigelshoven, S., Ludwig, K.U., Herold, C., Mangold, E., Becker, T., Kruse, R., Knapp, M., Nöthen, M.M.

“…Summary Background Male pattern baldness (androgenetic alopecia, AGA) is a highly heritable trait and the most common form of hair loss in humans. Eight…”
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Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness by Brockschmidt, F.F., Heilmann, S., Ellis, J.A., Eigelshoven, S., Hanneken, S., Herold, C., Moebus, S., Alblas, M.A., Lippke, B., Kluck, N., Priebe, L., Degenhardt, F.A., Jamra, R.A., Meesters, C., Jöckel, K.-H., Erbel, R., Harrap, S., Schumacher, J., Fröhlich, H., Kruse, R., Hillmer, A.M., Becker, T., Nöthen, M.M.

“…Summary Background  Male‐pattern baldness (androgenetic alopecia, AGA) is the most common form of hair loss among humans. Research has shown that it is caused…”
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O100 : The hepatic microenvironment induces a CSC phenotype and determines the prognosis of HCC patients by Castven, D, Fischer, M, Heinrich, S, Andersen, J.B, Sprinzl, M.F, Gockel, I, Heilmann, S, Wörns, M.A, Thorgeirsson, S.S, Galle, P.R, Lang, H, Marquardt, J.U

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Fine mapping of the human AR/EDA2R locus in androgenetic alopecia by Brockschmidt, F.F., Hillmer, A.M., Eigelshoven, S., Hanneken, S., Heilmann, S., Barth, S., Herold, C., Becker, T., Kruse, R., Nöthen, M.M.

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Morphine metabolism in human skin microsomes by Heilmann, S, Küchler, S, Schäfer-Korting, M

“…For patients with severe skin wounds, topically applied morphine is an option to induce efficient analgesia due to the presence of opioid receptors in the…”
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Bruchmechanische Untersuchung der Titan‐PEEK‐Grenzfläche in thermoplastischen Titan‐CF/PEEK‐Laminaten durch Mixed‐Mode‐Bending‐Versuche by Schulze, K., Hausmann, J., Heilmann, S., Wielage, B.

“…Adhäsions‐ und Versagensmechanismen an der Titan‐PEEK‐Grenzfläche in Ti‐CF/PEEK‐Laminaten wurden im Mixed‐Mode‐Bending‐Versuch bei überlagerter Mode I‐ und…”
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No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia by Heilmann, S., Nyholt, D.R., Brockschmidt, F.F., Hillmer, A.M., Herold, C., Becker, T., Martin, N.G., Nöthen, M.M.

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Clinical presentation of qualitative olfactory dysfunction by FRASNELLI, J, LANDIS, B. N, HEILMANN, S, HAUSWALD, B, HÜTTENBRINK, K. B, LACROIX, J. S, LEOPOLD, D. A, HUMMEL, T

“…Many patients with olfactory dysfunction not only experience quantitative reduction of olfactory function, but also suffer from distorted olfactory sensations…”
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A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1 by Vijayakrishnan, J, Kumar, R, Henrion, M Y R, Moorman, A V, Rachakonda, P S, Hosen, I, da Silva Filho, M I, Holroyd, A, Dobbins, S E, Koehler, R, Thomsen, H, Irving, J A, Allan, J M, Lightfoot, T, Roman, E, Kinsey, S E, Sheridan, E, Thompson, P D, Hoffmann, P, Nöthen, M M, Heilmann-Heimbach, S, Jöckel, K H, Greaves, M, Harrison, C J, Bartram, C R, Schrappe, M, Stanulla, M, Hemminki, K, Houlston, R S

“…Genome-wide association studies (GWASs) have shown that common genetic variation contributes to the heritable risk of childhood acute lymphoblastic leukemia…”
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MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration by Stüssel, L.G., Hollstein, R., Laugsch, M., Hochfeld, L.M., Welzenbach, J., Schröder, J., Thieme, F., Ishorst, N., Romero, R. Olmos, Weinhold, L., Hess, T., Gehlen, J., Mostowska, A., Heilmann-Heimbach, S., Mangold, E., Rada-Iglesias, A., Knapp, M., Schaaf, C.P., Ludwig, K.U.

“…Nonsyndromic cleft lip with or without palate (nsCL/P) ranks among the most common human birth defects and has a multifactorial etiology. Human neural crest…”
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Microdeletions Including FMR1 in Three Female Patients with Intellectual Disability - Further Delineation of the Phenotype and Expression Studies by Zink, A.M., Wohlleber, E., Engels, H., Rødningen, O.K., Ravn, K., Heilmann, S., Rehnitz, J., Katzorke, N., Kraus, C., Blichfeldt, S., Hoffmann, P., Reutter, H., Brockschmidt, F.F., Kreiß-Nachtsheim, M., Vogt, P.H., Prescott, T.E., Tümer, Z., Lee, J.A.

“…Fragile X syndrome (FXS) is one of the most common causes of intellectual disability/developmental delay (ID/DD), especially in males. It is caused most often…”
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The serotonin receptor 3E variant is a risk factor for female IBS-D by Fritz, Nikola, Berens, Sabrina, Dong, Yuanjun, Martínez, Cristina, Schmitteckert, Stefanie, Houghton, Lesley A., Goebel-Stengel, Miriam, Wahl, Verena, Kabisch, Maria, Götze, Dorothea, D’Amato, Mauro, Zheng, Tenghao, Röth, Ralph, Mönnikes, Hubert, Tesarz, Jonas, Engel, Felicitas, Gauss, Annika, Raithel, Martin, Andresen, Viola, Keller, Jutta, Frieling, Thomas, Pehl, Christian, Stein-Thöringer, Christoph, Clarke, Gerard, Kennedy, Paul J., Cryan, John F., Dinan, Timothy G., Quigley, Eamonn M. M., Spiller, Robin, Beltrán, Caroll, Madrid, Ana María, Torres, Verónica, Mayer, Emeran A., Sayuk, Gregory, Gazouli, Maria, Karamanolis, George, Bustamante, Mariona, Estivil, Xavier, Rabionet, Raquel, Hoffmann, Per, Nöthen, Markus M., Heilmann-Heimbach, Stefanie, Schmidt, Börge, Franke, André, Lieb, Wolfgang, Herzog, Wolfgang, Boeckxstaens, Guy, Wouters, Mira M., Simrén, Magnus, Rappold, Gudrun A., Vicario, Maria, Santos, Javier, Schaefert, Rainer, Lorenzo-Bermejo, Justo, Niesler, Beate

“…Irritable bowel syndrome (IBS) is a gut-brain disorder of multifactorial origin. Evidence of disturbed serotonergic function in IBS accumulated for the 5-HT 3…”
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Genome-wide association study of pathological gambling by Lang, M, Leménager, T, Streit, F, Fauth-Bühler, M, Frank, J, Juraeva, D, Witt, S.H, Degenhardt, F, Hofmann, A, Heilmann-Heimbach, S, Kiefer, F, Brors, B, Grabe, H.-J, John, U, Bischof, A, Bischof, G, Völker, U, Homuth, G, Beutel, M, Lind, P.A, Medland, S.E, Slutske, W.S, Martin, N.G, Völzke, H, Nöthen, M.M, Meyer, C, Rumpf, H.-J, Wurst, F.M, Rietschel, M, Mann, K.F

“…Abstract Background Pathological gambling is a behavioural addiction with negative economic, social, and psychological consequences. Identification of…”
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Traffic conflicts and their contextual factors when riding conventional vs. electric bicycles by Petzoldt, Tibor, Schleinitz, Katja, Heilmann, Sarah, Gehlert, Tina

“…•E-bikes faster than conventional bicycles, leading to concerns about traffic safety.•Investigation of traffic conflicts of e-bikes and bicycles with…”
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