Keyword

hypopigmentation

Description: Hypopigmentation is a reduction in skin pigmentation that makes an area lighter than the surrounding skin or its usual baseline color.

Primary topic: melanin and skin pigmentation (30%)

Wikidata ID: wiki/Q1291366

OpenAlex ID: keywords/hypopigmentation

Prader‐Willi syndrome: Current understanding of cause and diagnosis

1990 · Merlin G. Butler · American Journal of Medical Genetics · 583

Identification and mutation analysis of the complete gene for Chediak–Higashi syndrome

1996 · Deborah L. Nagle, Mohammad A. Karim, et al. · Nature Genetics · 539

Complications of Carbon Dioxide Laser Resurfacing. An Evaluation of 500 Patients

1998 · CHRISTOPHER A. NANNI, TINA S. ALSTER · Dermatologic Surgery · 489

The treatment of melasma: A review of clinical trials

2006 · Aditya K. Gupta, Melissa D. Gover, et al. · Journal of the American Academy of Dermatology · 471

Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice

2001 · Michael G. Anderson, Richard S. Smith, et al. · Nature Genetics · 453

Pembrolizumab Cutaneous Adverse Events and Their Association With Disease Progression

2015 · Martina Sanlorenzo, Igor Vujic, et al. · JAMA Dermatology · 449

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The BACE1 inhibitor verubecestat (MK-8931) reduces CNS β-amyloid in animal models and in Alzheimer’s disease patients

2016 · Matthew E. Kennedy, Andrew W. Stamford, et al. · Science Translational Medicine · 429

Efficacy of pazopanib in progressive, radioiodine-refractory, metastatic differentiated thyroid cancers: results of a phase 2 consortium study

2010 · Keith C Bible, Vera J Suman, et al. · The Lancet Oncology · 421

A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism

1993 · Eugene M. Rinchik, Scott J. Bultman, et al. · Nature · 415

Dermoscopy in General Dermatology: A Practical Overview

2016 · Enzo Errichetti, Giuseppe Stinco · Dermatology and Therapy · 404

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Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3

2000 · S. Brian Potterf, Minao Furumura, et al. · Human Genetics · 379

The Short- and Long-Term Side Effects of Carbon Dioxide Laser Resurfacing

1997 · LEONARD J. BERNSTEIN, ARIELLE N. B. KAUVAR, et al. · Dermatologic Surgery · 378

Chediak-Higashi syndrome

2008 · Jerry Kaplan, Ivana De Domenico, et al. · Current Opinion in Hematology · 364

Mutations in the Human Orthologue of the Mouse underwhite Gene (uw) Underlie a New Form of Oculocutaneous Albinism, OCA4

2001 · J.M. Newton, Orit Cohen-Barak, et al. · The American Journal of Human Genetics · 357

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Treatment Response of Keloidal and Hypertrophic Sternotomy Scars

2002 · Woraphong Manuskiatti · Archives of Dermatology · 352

The pigmentary system : physiology and pathophysiology

1998 · James J. Nordlund · 352

The Relationship of Arsenic Levels in Drinking Water and the Prevalence Rate of Skin Lesions in Bangladesh

1999 · M Tondel, M Rahman, et al. · Environmental Health Perspectives · 341

On the etiology of vitiligo and gray hair

1971 · Aaron B. Lerner · The American Journal of Medicine · 299

Histologic analysis of photochemical lesions produced in rhesus retina by short-wave-length light.

1978 · W T Ham, J J Ruffolo, et al. · PubMed · 293

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

2003 · Gaël Ménasché, Chen Hsuan Ho, et al. · Journal of Clinical Investigation · 291

Epistatic relationship between Waardenburg Syndrome genes MITF and PAX3

1998 · Atsushi Watanabe, Kazuhisa Takeda, et al. · Nature Genetics · 290

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

2003 · Gaël Ménasché, Chen Hsuan Ho, et al. · Journal of Clinical Investigation · 289

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Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy

2012 · Thomas Cullup, Ay Lin Kho, et al. · Nature Genetics · 283

Comparison of Erbium:YAG and Carbon Dioxide Lasers in Resurfacing of Facial Rhytides

1999 · Khalil A. Khatri, Victor Ross, et al. · Archives of Dermatology · 266

Cell-specific ATP7A transport sustains copper-dependent tyrosinase activity in melanosomes

2008 · Subba Rao Gangi Setty, Danièle Tenza, et al. · Nature · 265

Works count: 5,697

Citation count: 80,530