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Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness. [electronic resource] by
- Hillmer, Axel M
- Freudenberg, Jan
- Myles, Sean
- Herms, Stefan
- Tang, Kun
- Hughes, David A
- Brockschmidt, Felix F
- Ruan, Yijun
- Stoneking, Mark
- Nöthen, Markus M
Producer: 20090908
In:
Human genetics vol. 126
Availability: No items available.
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Loss of the SWI/SNF-ATPase subunit members SMARCF1 (ARID1A), SMARCA2 (BRM), SMARCA4 (BRG1) and SMARCB1 (INI1) in oesophageal adenocarcinoma. [electronic resource] by
- Schallenberg, Simon
- Bork, Julian
- Essakly, Ahlem
- Alakus, Hakan
- Buettner, Reinhard
- Hillmer, Axel M
- Bruns, Christiane
- Schroeder, Wolfgang
- Zander, Thomas
- Loeser, Heike
- Gebauer, Florian
- Quaas, Alexander
Producer: 20200615
In:
BMC cancer vol. 20
Availability: No items available.
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10.
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PIK3CA and KRAS Amplification in Esophageal Adenocarcinoma and their Impact on the Inflammatory Tumor Microenvironment and Prognosis. [electronic resource] by
- Essakly, Ahlem
- Loeser, Heike
- Kraemer, Max
- Alakus, Hakan
- Chon, Seung-Hun
- Zander, Thomas
- Buettner, Reinhard
- Hillmer, Axel M
- Bruns, Christiane J
- Schroeder, Wolfgang
- Gebauer, Florian
- Quaas, Alexander
Publication details: Translational oncology Feb 2020
In:
Translational oncology vol. 13
Availability: No items available.
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A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. [electronic resource] by
- Abraham, Richard
- Moskvina, Valentina
- Sims, Rebecca
- Hollingworth, Paul
- Morgan, Angharad
- Georgieva, Lyudmila
- Dowzell, Kimberley
- Cichon, Sven
- Hillmer, Axel M
- O'Donovan, Michael C
- Williams, Julie
- Owen, Michael J
- Kirov, George
Producer: 20090723
In:
BMC medical genomics vol. 1
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Novel therapeutic targets on the horizon for lung cancer. [electronic resource] by
- Tan, Wan-Ling
- Jain, Amit
- Takano, Angela
- Newell, Evan W
- Iyer, N Gopalakrishna
- Lim, Wan-Teck
- Tan, Eng-Huat
- Zhai, Weiwei
- Hillmer, Axel M
- Tam, Wai-Leong
- Tan, Daniel S W
Producer: 20170605
In:
The Lancet. Oncology vol. 17
Availability: No items available.
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Concurrent Single-Cell RNA and Targeted DNA Sequencing on an Automated Platform for Comeasurement of Genomic and Transcriptomic Signatures. [electronic resource] by
- Kong, Say Li
- Li, Huipeng
- Tai, Joyce A
- Courtois, Elise T
- Poh, Huay Mei
- Lau, Dawn Pingxi
- Haw, Yu Xuan
- Iyer, Narayanan Gopalakrishna
- Tan, Daniel Shao Weng
- Prabhakar, Shyam
- Ruff, Dave
- Hillmer, Axel M
Producer: 20191121
In:
Clinical chemistry vol. 65
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G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth. [electronic resource] by
- Pasternack, Sandra M
- von Kügelgen, Ivar
- Al Aboud, Khalid
- Lee, Young-Ae
- Rüschendorf, Franz
- Voss, Katrin
- Hillmer, Axel M
- Molderings, Gerhard J
- Franz, Thomas
- Ramirez, Alfredo
- Nürnberg, Peter
- Nöthen, Markus M
- Betz, Regina C
Producer: 20080402
In:
Nature genetics vol. 40
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Impaired development of neural-crest cell-derived organs and intellectual disability caused by MED13L haploinsufficiency. [electronic resource] by
- Utami, Kagistia Hana
- Winata, Cecilia Lanny
- Hillmer, Axel M
- Aksoy, Irene
- Long, Hoang Truong
- Liany, Herty
- Chew, Elaine G Y
- Mathavan, Sinnakaruppan
- Tay, Stacey K H
- Korzh, Vladimir
- Sarda, Pierre
- Davila, Sonia
- Cacheux, Valere
Producer: 20150626
In:
Human mutation vol. 35
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Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26. [electronic resource] by
- Hillmer, Axel M
- Flaquer, Antonia
- Hanneken, Sandra
- Eigelshoven, Sibylle
- Kortüm, Anne-Katrin
- Brockschmidt, Felix F
- Golla, Astrid
- Metzen, Christine
- Thiele, Holger
- Kolberg, Susanne
- Reinartz, Roman
- Betz, Regina C
- Ruzicka, Thomas
- Hennies, Hans Christian
- Kruse, Roland
- Nöthen, Markus M
Producer: 20080328
In:
American journal of human genetics vol. 82
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17.
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Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase. [electronic resource] by
- Ramirez, Alfredo
- Heimbach, André
- Gründemann, Jan
- Stiller, Barbara
- Hampshire, Dan
- Cid, L Pablo
- Goebel, Ingrid
- Mubaidin, Ammar F
- Wriekat, Abdul-Latif
- Roeper, Jochen
- Al-Din, Amir
- Hillmer, Axel M
- Karsak, Meliha
- Liss, Birgit
- Woods, C Geoffrey
- Behrens, Maria I
- Kubisch, Christian
Producer: 20061128
In:
Nature genetics vol. 38
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Loss-of-function mutations in the filaggrin gene and alopecia areata: strong risk factor for a severe course of disease in patients comorbid for atopic disease. [electronic resource] by
- Betz, Regina C
- Pforr, Jana
- Flaquer, Antonia
- Redler, Silke
- Hanneken, Sandra
- Eigelshoven, Sibylle
- Kortüm, Anne-Katrin
- Tüting, Thomas
- Lambert, Julien
- De Weert, Jozef
- Hillmer, Axel M
- Schmael, Christine
- Wienker, Thomas F
- Kruse, Roland
- Lutz, Gerhard
- Blaumeiser, Bettina
- Nöthen, Markus M
Producer: 20071029
In:
The Journal of investigative dermatology vol. 127
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19.
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Differential Expression between Human Dermal Papilla Cells from Balding and Non-Balding Scalps Reveals New Candidate Genes for Androgenetic Alopecia. [electronic resource] by
- Chew, Elaine G Y
- Tan, Joanna H J
- Bahta, Adiam W
- Ho, Bryan S-Y
- Liu, Xingliang
- Lim, Tze Chiun
- Sia, Yee Yen
- Bigliardi, Paul L
- Heilmann, Stefanie
- Wan, Andrew C A
- Nöthen, Markus M
- Philpott, Michael P
- Hillmer, Axel M
Producer: 20170717
In:
The Journal of investigative dermatology vol. 136
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The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations. [electronic resource] by
- Schumacher, Johannes
- Laje, Gonzalo
- Abou Jamra, Rami
- Becker, Tim
- Mühleisen, Thomas W
- Vasilescu, Catalina
- Mattheisen, Manuel
- Herms, Stefan
- Hoffmann, Per
- Hillmer, Axel M
- Georgi, Alexander
- Herold, Christine
- Schulze, Thomas G
- Propping, Peter
- Rietschel, Marcella
- McMahon, Francis J
- Nöthen, Markus M
- Cichon, Sven
Producer: 20090914
In:
Human molecular genetics vol. 18
Availability: No items available.
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