D. Bercovich

发表

Naegeli-franceschetti-jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in Krt14

J. Lugassy, P. Itin, A. Ishida-Yamamoto, 2022 .

Homozygosity of MSH2 c.1906G→C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I

D. Bercovich, H. Baris, I. Lerer, 2008, Familial Cancer.

Genotype/phenotype correlation in primary congenital glaucoma patients from different ethnic groups of the Israeli population.

D. Bercovich, C. Shochat, D. Walton, 2011, American journal of ophthalmology.

Mars can wait: facing the challenges of our civilization.

D. Bercovich, M. Gershwin, Geoffrey Goodman, 2014, The Israel Medical Association journal : IMAJ.

A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A

J. Bressler, L. Shaffer, A. Beaudet, 2004, American journal of medical genetics. Part A.

Cell lineage analysis of acute leukemia relapse uncovers the role of replication-rate heterogeneity and microsatellite instability.

E. Shapiro, C. Bloomfield, R. Adar, 2012, Blood.

A mutation in SNAP29, coding for a SNARE protein involved in intracellular trafficking, causes a novel neurocutaneous syndrome characterized by cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma.

Hanna Mandel, Eli Sprecher, H. Mandel, 2005, American journal of human genetics.

Molecular characterization of three novel Fanconi anemia mutations in Israeli Arabs

D. Bercovich, H. Tamary, H. Toledano, 2004, European journal of haematology.

Interleukin 7 and thymic stromal lymphopoietin: from immunity to leukemia

D. Bercovich, S. Izraeli, C. Shochat, 2013, Cellular and Molecular Life Sciences.

Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome

G. Wainreb, A. Green, A. Borkhardt, 2008, The Lancet.

SFB-based S-haplotyping of apricot (Prunus armeniaca) with DHPLC

D. Bercovich, R. Stern, M. Goldway, 2009 .

A case of Ververi‐Brady syndrome due to QRICH1 loss of function and the literature review

D. Bercovich, R. Gershoni-baruch, S. Horn-Saban, 2021, American journal of medical genetics. Part A.

Hereditary Skin Cancer

D. Bercovich, I. Kedar, 2016 .

The two-brains hypothesis: Implications for consciousness

R. R. Poznanski, D. Bercovich, L. Cacha, 2016 .

The Two-Brains Hypothesis: Towards a guide for brain-brain and brain-machine interfaces.

R. R. Poznanski, D. Bercovich, L. Cacha, 2015, Journal of integrative neuroscience.

Facing the challenges of our civilization

D. Bercovich, M. Gershwin, Geoffrey Goodman, 2022 .

Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity

D. Bercovich, H. Baris, I. Lerer, 2016, Pediatric blood & cancer.

Mutations of JAK 2 in acute lymphoblastic leukaemias associated with Down ’ s syndrome

G. Wainreb, A. Green, A. Borkhardt, 2008 .

An Ashkenazi founder mutation in the MSH6 gene leading to HNPCC

D. Bercovich, I. Lerer, Y. Goldberg, 2010, Familial Cancer.

A novel BRCA-1 mutation in Arab kindred from east Jerusalem with breast and ovarian cancer

D. Bercovich, A. Nissan, L. Kadouri, 2007, BMC Cancer.

Mutation Screening andAssociation Study of theCandidate ProstateCancer Susceptibility GenesMSR1,PTEN, andKLF6

D. Bercovich, A. Orr-Urtreger, A. Bar‐Shira, 2006 .

A novel heterozygous IGF-1 receptor mutation associated with hypoglycemia

M. Phillip, D. Bercovich, H. Werner, 2017, Endocrine connections.

Use of denaturing HPLC to provide efficient detection of mutations causing familial hypercholesterolemia.

A. Beaudet, D. Bercovich, C. Ballantyne, 2002, Clinical chemistry.

Synergistic control of keratinocyte adhesion through muscarinic and nicotinic acetylcholine receptor subtypes.

A. Beaudet, J. Wess, D. Bercovich, 2004, Experimental cell research.

Central role of α7 nicotinic receptor in differentiation of the stratified squamous epithelium

D. Bercovich, W. Kummer, A. Orr-Urtreger, 2002, The Journal of cell biology.

Gain-of-function mutations in interleukin-7 receptor-α (IL7R) in childhood acute lymphoblastic leukemias

M. Muckenthaler, M. Schrappe, D. Bercovich, 2011, The Journal of experimental medicine.

Genotype–phenotype correlations analysis of mutations in the phenylalanine hydroxylase (PAH) gene

D. Bercovich, Y. Anikster, R. Loewenthal, 2008, Journal of Human Genetics.

MECP2 Mutations in Israel: Implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndrome

D. Bercovich, A. Orr-Urtreger, Y. Yaron, 2002, Human mutation.

Screening for familial dysautonomia in Israel: evidence for higher carrier rate among Polish Ashkenazi Jews.

D. Bercovich, O. Aizenstein, A. Orr-Urtreger, 2003, Genetic testing.

Denaturing high-performance liquid chromatography for the detection of mutations and polymorphisms in UBE3A.

A. Beaudet, D. Bercovich, A. Beaudet, 2003, Genetic testing.

Outbreak following a Vaccination Campaign Changing Nature of a Meningococcal Molecular Epidemiological Analysis of the

Keller, J. Lupski, A. Beaudet, 2002 .

A protocol for genetic evaluation of patients with multiple colorectal adenomas and without evidence of APC gene mutation.

Z. Halpern, D. Bercovich, C. Shochat, 2010, The Israel Medical Association journal : IMAJ.

Case Study: A Human Pre-Natal Experiment in 1944—“Do No Harm”

D. Bercovich, G. Goodman, K. Shlush, 2016 .

Extreme Short Stature and Severe Neurological Impairment in a 17-Year-Old Male With Untreated Combined Pituitary Hormone Deficiency Due to POU1F1 Mutation

D. Bercovich, S. Amselem, M. Legendre, 2019, Front. Endocrinol..

A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosis.

D. Geiger, M. Indelman, D. Bercovich, 2006, American journal of human genetics.

The Many Faces of Glut1 Deficiency Syndrome

D. Bercovich, Y. Anikster, S. Marcu, 2014, Journal of child neurology.

A novel founder mutation in the RNASEL gene, 471delAAAG, is associated with prostate cancer in Ashkenazi Jews.

G. Rennert, D. Bercovich, L. Kadouri, 2002, American journal of human genetics.

Severe infantile male encephalopathy is a result of early post‐zygotic WDR45 somatic mutation

D. Bercovich, A. Shaag, O. Elpeleg, 2016, Clinical genetics.

Gain-of-function mutations in interleukin-7 receptor-α (IL7R) in childhood acute lymphoblastic leukemias

M. Muckenthaler, M. Schrappe, D. Bercovich, 2011, The Journal of Experimental Medicine.

Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21.

A. Teigler‐Schlegel, O. Haas, D. Bercovich, 2003, Blood.

DHPLC screening for mutations in progressive familial intrahepatic cholestasis patients

D. Bercovich, Y. Anikster, R. Shamir, 2010, Journal of Human Genetics.

Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BFM Study Group.

E. Domany, A. Borkhardt, D. Bercovich, 2010, Blood.

High Prevalence of Hearing Impairment in Primary Congenital Hypothyroidism

S. Almashanu, D. Bercovich, R. Spiegel, 2020, European Thyroid Journal.

Interleukin 7 and thymic stromal lymphopoietin: from immunity to leukemia

D. Bercovich, S. Izraeli, C. Shochat, 2014, Cellular and Molecular Life Sciences.

Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure

D. Bercovich, Dvir Dahary, S. Gulsuner, 2015, Journal of Medical Genetics.

The significance of human spermatozoa vacuoles can be elucidated by a novel procedure of array comparative genomic hybridization

D. Bercovich, Yossy Machluf, A. Berkovitz, 2018, Human reproduction.

RASA1 mutations may cause hereditary capillary malformations without arteriovenous malformations

D. Bercovich, E. Sprecher, D. Hershkovitz, 2008, The British journal of dermatology.

Melanin directly converts light for vertebrate metabolic use: heuristic thoughts on birds, Icarus and dark human skin.

D. Bercovich, G. Goodman, 2008, Medical hypotheses.

Fullerene and the origin of life.

D. Bercovich, M. Gershwin, Geoffrey Goodman, 2012, The Israel Medical Association journal : IMAJ.

Autosomal-recessive hypophosphatemic rickets is associated with an inactivation mutation in the ENPP1 gene.

V. Chalifa-Caspi, D. Bercovich, E. Manor, 2010, American journal of human genetics.

The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation

C. Walsh, D. Bercovich, T. Olender, 2005, Journal of Medical Genetics.

The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease

Nir Giladi, D. Bercovich, T. Gurevich, 2007, Neurology.

POLD1 and POLE Gene Mutations in Jewish Cohorts of Early-Onset Colorectal Cancer and of Multiple Colorectal Adenomas

S. Carmi, D. Bercovich, N. Gluck, 2018, Diseases of the colon and rectum.

mutated JAK2: a report from the International BFM Study Group disease in which aberrant expression of CRLF2 is associated with Down syndrome acute lymphoblastic leukemia, a highly heterogeneous

E. Domany, A. Borkhardt, D. Bercovich, 2013 .

A Mutation Analysis of the Phenylalanine Hydroxylase (PAH) Gene in the Israeli Population

D. Bercovich, Y. Anikster, R. Loewenthal, 2008, Annals of human genetics.

Analysis of genetic polymorphisms in acetylcholinesterase as reflected in different populations.

J. Beckmann, J. Sussman, A. Korczyn, 2005, Current Alzheimer research.

A paradigm for single nucleotide polymorphism analysis: The case of the acetylcholinesterase gene

J. Beckmann, J. Sussman, A. Korczyn, 2004, Human mutation.

Novel activating mutations lacking cysteine in type I cytokine receptors in acute lymphoblastic leukemia.

N. Ben-Tal, M. Muckenthaler, J. Twizere, 2014, Blood.

Functional polymorphisms in the human β4 subunit of nicotinic acetylcholine receptors

A. Beaudet, M. Biasi, D. Bercovich, 2005, Neurogenetics.

RNASEL Mutation Screening and Association Study in Ashkenazi and Non-Ashkenazi Prostate Cancer Patients

G. Rennert, D. Bercovich, L. Kadouri, 2006, Cancer Epidemiology Biomarkers & Prevention.

Pregnancy and lactation after breast cancer elevate plasma prolactin, do not shorten and may prolong survival.

D. Bercovich, G. Goodman, 2009, Medical hypotheses.

Dispersal of an ancient retroposon in the TP53 promoter of Bovidae: phylogeny, novel mechanisms, and potential implications for cow milk persistency

S. Ben-Dor, D. Bercovich, I. Ben-Shlomo, 2015, BMC Genomics.

Mutations in olfactory signal transduction genes are not a major cause of human congenital general anosmia.

D. Lancet, D. Bercovich, E. Feldmesser, 2007, Chemical senses.

Familial adenomatous polyposis

D. Bercovich, P. Rozen, Dani Bercovich, 2009, Orphanet journal of rare diseases.

Quantitative ratio of primer pairs and annealing temperature affecting PCR products in duplex amplification.

D. Bercovich, Y. Gruenbaum, Y. Plotsky, 1999, BioTechniques.

Mitochondrial pro-apoptotic ARTS protein is lost in the majority of acute lymphoblastic leukemia patients

Asaf Rotem, D. Bercovich, R. Elhasid, 2004, Oncogene.

Prolactin does not cause breast cancer and may prevent it or be therapeutic in some conditions.

D. Bercovich, G. Goodman, 2008, Medical hypotheses.

Electromagnetic induction between axons and their schwann cell myelin-protein sheaths.

D. Bercovich, G. Goodman, 2013, Journal of integrative neuroscience.

KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome.

J. Lugassy, P. Itin, D. Bercovich, 2008, The Journal of investigative dermatology.

Central Role of Fibroblast α3 Nicotinic Acetylcholine Receptor in Mediating Cutaneous Effects of Nicotine

A. Beaudet, D. Bercovich, A. Orr-Urtreger, 2003, Laboratory Investigation.

Mammal domestication and the symbiotic spectrum

D. Bercovich, I. Ben-Shlomo, Yossy Machluf, 2017, Proceedings of the National Academy of Sciences.

Increased risk for colorectal adenomas and cancer in mono-allelic MUTYH mutation carriers: results from a cohort of North-African Jews

Z. Halpern, D. Bercovich, Yael Etzion Daniel, 2015, Familial Cancer.

Familial Central Hypothyroidism Caused by a Novel IGSF1 Gene Mutation.

D. Bercovich, D. Bernard, Y. Tenenbaum‐Rakover, 2016, Thyroid : official journal of the American Thyroid Association.

Mutation screening and association study of the candidate prostate cancer susceptibility genes MSR1, PTEN, and KLF6

D. Bercovich, A. Orr-Urtreger, A. Bar‐Shira, 2006, The Prostate.

Mutation spectrum in HNPCC in the Israeli population

E. Pikarski, D. Bercovich, A. Nissan, 2008, Familial Cancer.

The association of common SNPs and haplotypes in the CETP and MDR1 genes with lipids response to fluvastatin in familial hypercholesterolemia.

L. Kleinberg, D. Bercovich, Y. Friedlander, 2006, Atherosclerosis.

Frequency of canine nt230(del4) MDR1 mutation in prone pure breeds, their crosses and mongrels in Israel - insights from a worldwide comparative perspective.

D. Bercovich, I. Ben-Shlomo, Yossy Machluf, 2017, BMC Veterinary Research.

Functional role of alpha7 nicotinic receptor in physiological control of cutaneous homeostasis.

D. Bercovich, A. Orr-Urtreger, D. Vetter, 2003, Life sciences.

acute lymphoblastic leukemia Novel activating mutations lacking cysteine in type I cytokine receptors in

N. Ben-Tal, J. Twizere, S. Constantinescu, 2014 .

Long-term outcome of loss-of-function mutations in thyrotropin receptor gene.

S. Almashanu, D. Bercovich, S. Refetoff, 2015, Thyroid : official journal of the American Thyroid Association.

Molecular analysis of the APC gene in 71 Israeli families: 17 novel mutations

D. Bercovich, A. Orr-Urtreger, Y. Yaron, 2002, Human mutation.

Two BRCA1/2 founder mutations in Jews of Sephardic origin

D. Bercovich, I. Lerer, Y. Goldberg, 2011, Familial Cancer.

nonsyndromic mental retardation C2 domains, is involved in autosomal recessive The CC2D1A, a member of a new gene family with

C. Walsh, D. Bercovich, T. Olender, 2005 .

Molecular Epidemiological Analysis of the Changing Nature of a Meningococcal Outbreak following a Vaccination Campaign

J. Lupski, A. Beaudet, D. Behar, 2002, Journal of Clinical Microbiology.

DOWN'S Syndrome Acute Lymphoblastic LEUKEMIA: A HIGHLY Heterogeneous DISEASE DRIVEN by an Aberrant CRLF2/JAK2 Cooperation – A REPORT FROM the Ibfm-STUDY GROUP.

E. Domany, D. Bercovich, G. Kronnie, 2009 .

Characterization of the human β4 nAChR gene and polymorphisms in CHRNA3 and CHRNB4

A. Beaudet, D. Bercovich, E. Lev-Lehman, 2001, Journal of Human Genetics.

Increased risk for colorectal adenomas and cancer in mono-allelic MUTYH mutation carriers: results from a cohort of North-African Jews

Zamir Halpern, Guy Rosner, Revital Kariv, 2015, Familial Cancer.

Novel activating mutations lacking cysteine in type I cytokine receptors in acute lymphoblastic leukemia.

N. Ben-Tal, M. Muckenthaler, J. Twizere, 2014, Blood.

Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BFM Study Group.

E. Domany, R. Arceci, A. Borkhardt, 2010, Blood.

The two-brains hypothesis: Implications for consciousness

R. Penrose, S. Hameroff, D. Bercovich, 2016 .

Autosomal-recessive hypophosphatemic rickets is associated with an inactivation mutation in the ENPP1 gene.

V. Chalifa-Caspi, D. Bercovich, E. Manor, 2010, American journal of human genetics.

Melanin directly converts light for vertebrate metabolic use: heuristic thoughts on birds, Icarus and dark human skin.

D. Bercovich, G. Goodman, 2008, Medical hypotheses.

Immunity, Life and Dancing Starlings: A Physician's Perspective.

D. Bercovich, M. Gershwin, Geoffrey Goodman, 2016, The Israel Medical Association journal : IMAJ.

RASA1 mutations may cause hereditary capillary malformations without arteriovenous malformations

D. Bercovich, E. Sprecher, D. Hershkovitz, 2008, The British journal of dermatology.